메뉴 건너뛰기




Volumn 116, Issue 3, 2016, Pages 1094-1138

Efficient Separation of Enantiomers Using Stereoregular Chiral Polymers

Author keywords

[No Author keywords available]

Indexed keywords

COLUMN CHROMATOGRAPHY; EFFLUENT TREATMENT; GAS CHROMATOGRAPHY; STEREOCHEMISTRY; SUPERCRITICAL FLUIDS;

EID: 84958093894     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/acs.chemrev.5b00317     Document Type: Review
Times cited : (596)

References (443)
  • 1
    • 0023639698 scopus 로고
    • Bias in Pharmacokinetics and Clinical Pharmacology
    • Ariëns, E. J.; Wuis, E. W. Bias in Pharmacokinetics and Clinical Pharmacology Clin. Pharmacol. Ther. 1987, 42, 361-363 10.1038/clpt.1987.163
    • (1987) Clin. Pharmacol. Ther. , vol.42 , pp. 361-363
    • Ariëns, E.J.1    Wuis, E.W.2
  • 5
    • 84902422003 scopus 로고    scopus 로고
    • Elsevier: Amsterdam, Separations and Analysis
    • In Comprehensive Chirality; Carreira, E. M.; Yamamoto, H., Eds.; Elsevier: Amsterdam, 2012; Vol. 8, Separations and Analysis.
    • (2012) Comprehensive Chirality , vol.8
    • Carreira, E.M.1    Yamamoto, H.2
  • 9
    • 1542350269 scopus 로고    scopus 로고
    • Optically Active Polymers for Chiral Separation
    • Yamamoto, C.; Okamoto, Y. Optically Active Polymers for Chiral Separation Bull. Chem. Soc. Jpn. 2004, 77, 227-257 10.1246/bcsj.77.227
    • (2004) Bull. Chem. Soc. Jpn. , vol.77 , pp. 227-257
    • Yamamoto, C.1    Okamoto, Y.2
  • 10
    • 0035847205 scopus 로고    scopus 로고
    • Enantioselective Chromatography as a Powerful Alternative for the Preparation of Drug Enantiomers
    • Francotte, E. Enantioselective Chromatography as a Powerful Alternative for the Preparation of Drug Enantiomers J. Chromatogr. A 2001, 906, 379-397 10.1016/S0021-9673(00)00951-1
    • (2001) J. Chromatogr. A , vol.906 , pp. 379-397
    • Francotte, E.1
  • 11
    • 17044426351 scopus 로고    scopus 로고
    • A Practical Guide to HPLC Enantioseparations for Pharmaceutical Compounds
    • Thompson, R. A Practical Guide to HPLC Enantioseparations for Pharmaceutical Compounds J. Liq. Chromatogr. Relat. Technol. 2005, 28, 1215-1231 10.1081/JLC-200053033
    • (2005) J. Liq. Chromatogr. Relat. Technol. , vol.28 , pp. 1215-1231
    • Thompson, R.1
  • 12
    • 0035847276 scopus 로고    scopus 로고
    • Optically Active Synthetic Polymers as Chiral Stationary Phases in HPLC
    • Nakano, T. Optically Active Synthetic Polymers as Chiral Stationary Phases in HPLC J. Chromatogr. A 2001, 906, 205-225 10.1016/S0021-9673(00)00944-4
    • (2001) J. Chromatogr. A , vol.906 , pp. 205-225
    • Nakano, T.1
  • 14
    • 0026834334 scopus 로고
    • Chiral Separations by High-Performance Liquid Chromatography
    • Taylor, D. R.; Maher, K. Chiral Separations by High-Performance Liquid Chromatography J. Chromatogr. Sci. 1992, 30, 67-85 10.1093/chromsci/30.3.67
    • (1992) J. Chromatogr. Sci. , vol.30 , pp. 67-85
    • Taylor, D.R.1    Maher, K.2
  • 15
    • 11744286228 scopus 로고
    • Considerations of Chiral Recognition Relevant to the Liquid Chromatography Separation of Enantiomers
    • Pirkle, W. H.; Pochapsky, T. C. Considerations of Chiral Recognition Relevant to the Liquid Chromatography Separation of Enantiomers Chem. Rev. 1989, 89, 347-362 10.1021/cr00092a006
    • (1989) Chem. Rev. , vol.89 , pp. 347-362
    • Pirkle, W.H.1    Pochapsky, T.C.2
  • 16
    • 56549116899 scopus 로고    scopus 로고
    • Chiral HPLC for Efficient Resolution of Enantiomers
    • Okamoto, Y.; Ikai, T. Chiral HPLC for Efficient Resolution of Enantiomers Chem. Soc. Rev. 2008, 37, 2593-2608 10.1039/b808881k
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 2593-2608
    • Okamoto, Y.1    Ikai, T.2
  • 17
    • 84855960441 scopus 로고    scopus 로고
    • Chiral Separations: A Review of Current Topics and Trends
    • Ward, T. J.; Ward, K. D. Chiral Separations: A Review of Current Topics and Trends Anal. Chem. 2012, 84, 626-635 10.1021/ac202892w
    • (2012) Anal. Chem. , vol.84 , pp. 626-635
    • Ward, T.J.1    Ward, K.D.2
  • 18
    • 84870315859 scopus 로고    scopus 로고
    • Recent Developments on Polysaccharide-Based Chiral Stationary Phases for Liquid-Phase Separation of Enantiomers
    • Chankvetadze, B. Recent Developments on Polysaccharide-Based Chiral Stationary Phases for Liquid-Phase Separation of Enantiomers J. Chromatogr. A 2012, 1269, 26-51 10.1016/j.chroma.2012.10.033
    • (2012) J. Chromatogr. A , vol.1269 , pp. 26-51
    • Chankvetadze, B.1
  • 19
    • 0035847272 scopus 로고    scopus 로고
    • Separation of Enantiomers: Needs, Challenges, Perspectives
    • Maier, N. M.; Franco, P.; Lindner, W. Separation of Enantiomers: Needs, Challenges, Perspectives J. Chromatogr. A 2001, 906, 3-33 10.1016/S0021-9673(00)00532-X
    • (2001) J. Chromatogr. A , vol.906 , pp. 3-33
    • Maier, N.M.1    Franco, P.2    Lindner, W.3
  • 20
    • 31444433430 scopus 로고    scopus 로고
    • Toda, F. Kluwer Academic Publishers: Dordrecht
    • Yamamoto, C.; Okamoto, Y. In Enantiomer Separation; Toda, F., Ed.; Kluwer Academic Publishers: Dordrecht, 2004; p 301-322.
    • (2004) Enantiomer Separation , pp. 301-322
    • Yamamoto, C.1    Okamoto, Y.2
  • 21
    • 36649036013 scopus 로고    scopus 로고
    • Polysaccharide Derivatives as Useful Chiral Stationary Phases in High-Performance Liquid Chromatography
    • Chen, X. M.; Yamamoto, C.; Okamoto, Y. Polysaccharide Derivatives as Useful Chiral Stationary Phases in High-Performance Liquid Chromatography Pure Appl. Chem. 2007, 79, 1561-1573 10.1351/pac200779091561
    • (2007) Pure Appl. Chem. , vol.79 , pp. 1561-1573
    • Chen, X.M.1    Yamamoto, C.2    Okamoto, Y.3
  • 22
    • 73249126525 scopus 로고    scopus 로고
    • Structure Control of Polysaccharide Derivatives for Efficient Separation of Enantiomers by Chromatography
    • Ikai, T.; Okamoto, Y. Structure Control of Polysaccharide Derivatives for Efficient Separation of Enantiomers by Chromatography Chem. Rev. 2009, 109, 6077-6101 10.1021/cr8005558
    • (2009) Chem. Rev. , vol.109 , pp. 6077-6101
    • Ikai, T.1    Okamoto, Y.2
  • 23
    • 0000237404 scopus 로고
    • NMR Determination of Enantiomeric Purity
    • Parker, D. NMR Determination of Enantiomeric Purity Chem. Rev. 1991, 91, 1441-1457 10.1021/cr00007a009
    • (1991) Chem. Rev. , vol.91 , pp. 1441-1457
    • Parker, D.1
  • 24
    • 84908109517 scopus 로고    scopus 로고
    • Synthesis and Application of Immobilized Polysaccharide-Based Chiral Stationary Phases for Enantioseparation by High-Performance Liquid Chromatography
    • Shen, J.; Ikai, T.; Okamoto, Y. Synthesis and Application of Immobilized Polysaccharide-Based Chiral Stationary Phases for Enantioseparation by High-Performance Liquid Chromatography J. Chromatogr. A 2014, 1363, 51-61 10.1016/j.chroma.2014.06.042
    • (2014) J. Chromatogr. A , vol.1363 , pp. 51-61
    • Shen, J.1    Ikai, T.2    Okamoto, Y.3
  • 26
    • 0023734924 scopus 로고
    • Chiral Resolution of a Series of 3-Thienylcyclohexylglycolic Acids by Liquid or Subcritical Fluid Chromatography. A Mechanistic Study
    • Macaudiere, P.; Caude, M.; Rosset, R.; Tambute, A. Chiral Resolution of a Series of 3-Thienylcyclohexylglycolic Acids by Liquid or Subcritical Fluid Chromatography. A Mechanistic Study J. Chromatogr. 1988, 450, 255-269 10.1016/S0021-9673(01)83579-2
    • (1988) J. Chromatogr. , vol.450 , pp. 255-269
    • Macaudiere, P.1    Caude, M.2    Rosset, R.3    Tambute, A.4
  • 27
    • 44349182545 scopus 로고    scopus 로고
    • Chiral Separations in Sub- and Supercritical Fluid Chromatography
    • Mangelings, D.; Heyden, Y. V. Chiral Separations in Sub- and Supercritical Fluid Chromatography J. Sep. Sci. 2008, 31, 1252-1273 10.1002/jssc.200700564
    • (2008) J. Sep. Sci. , vol.31 , pp. 1252-1273
    • Mangelings, D.1    Heyden, Y.V.2
  • 28
    • 44349111130 scopus 로고    scopus 로고
    • Clinical and Pharmaceutical Applications of Packed-Column Supercritical Fluid Chromatography
    • Abbott, E.; Veenstra, T. D.; Issaq, H. J. Clinical and Pharmaceutical Applications of Packed-Column Supercritical Fluid Chromatography J. Sep. Sci. 2008, 31, 1223-1230 10.1002/jssc.200700579
    • (2008) J. Sep. Sci. , vol.31 , pp. 1223-1230
    • Abbott, E.1    Veenstra, T.D.2    Issaq, H.J.3
  • 29
    • 18144400098 scopus 로고    scopus 로고
    • Enantioselective Separations by Packed Column Subcritical and Supercritical Fluid Chromatography
    • Phinney, K. W. Enantioselective Separations by Packed Column Subcritical and Supercritical Fluid Chromatography Anal. Bioanal. Chem. 2005, 382, 639-645 10.1007/s00216-005-3074-y
    • (2005) Anal. Bioanal. Chem. , vol.382 , pp. 639-645
    • Phinney, K.W.1
  • 30
    • 2342559912 scopus 로고    scopus 로고
    • High Efficiency Liquid and Super-/Subcritical Fluid-Based Enantiomeric Separations: An Overview
    • Liu, Y.; Lantz, A. W.; Armstrong, D. W. High Efficiency Liquid and Super-/Subcritical Fluid-Based Enantiomeric Separations: An Overview J. Liq. Chromatogr. Relat. Technol. 2004, 27, 1121-1178 10.1081/JLC-120030600
    • (2004) J. Liq. Chromatogr. Relat. Technol. , vol.27 , pp. 1121-1178
    • Liu, Y.1    Lantz, A.W.2    Armstrong, D.W.3
  • 31
    • 0011169213 scopus 로고
    • A New Method for Resolving a Racemic Compound
    • Henderson, G. M.; Rule, H. G. A New Method for Resolving a Racemic Compound Nature 1938, 141, 917-918 10.1038/141917b0
    • (1938) Nature , vol.141 , pp. 917-918
    • Henderson, G.M.1    Rule, H.G.2
  • 32
    • 0001295831 scopus 로고
    • Über die Spaltung der Tröger'schen Base in Optische Antipoden, ein Beitrag zur Stereochemie des Dreiwertigen Stickstoffs
    • Prelog, V.; Wieland, P. Über die Spaltung der Tröger'schen Base in Optische Antipoden, ein Beitrag zur Stereochemie des Dreiwertigen Stickstoffs Helv. Chim. Acta 1944, 27, 1127-1134 10.1002/hlca.194402701143
    • (1944) Helv. Chim. Acta , vol.27 , pp. 1127-1134
    • Prelog, V.1    Wieland, P.2
  • 33
    • 33947477854 scopus 로고
    • Optically Active Vinyl Polymers. VI. Chromatographic Resolution of Linear Polymers of (R)(S)-4-Methyl-1-hexene
    • Pino, P.; Ciadelli, F.; Lorenzi, G. P.; Natta, G. Optically Active Vinyl Polymers. VI. Chromatographic Resolution of Linear Polymers of (R)(S)-4-Methyl-1-hexene J. Am. Chem. Soc. 1962, 84, 1487-1488 10.1021/ja00867a028
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 1487-1488
    • Pino, P.1    Ciadelli, F.2    Lorenzi, G.P.3    Natta, G.4
  • 34
    • 37049126956 scopus 로고
    • Ligand Chromatography on Asymmetric Complex-Forming Sorbents as a New Method for Resolution of Racemates
    • Rogozhin, S. V.; Davankov, V. A. Ligand Chromatography on Asymmetric Complex-Forming Sorbents as a New Method for Resolution of Racemates J. Chem. Soc. D 1971, 490-490 10.1039/c2971000490a
    • (1971) J. Chem. Soc. D , pp. 490
    • Rogozhin, S.V.1    Davankov, V.A.2
  • 35
    • 84981919271 scopus 로고
    • Chromatographic Resolution of Racemates
    • Blaschke, G. Chromatographic Resolution of Racemates Angew. Chem., Int. Ed. Engl. 1971, 10, 520-521 10.1002/anie.197105202
    • (1971) Angew. Chem., Int. Ed. Engl. , vol.10 , pp. 520-521
    • Blaschke, G.1
  • 36
    • 0000146718 scopus 로고
    • Enzyme-Analogue Built Polymers and Their Use for the Resolution of Racemates
    • Wulff, G.; Sarhan, A.; Zabrocki, K. Enzyme-Analogue Built Polymers and Their Use for the Resolution of Racemates Tetrahedron Lett. 1973, 14, 4329-4332 10.1016/S0040-4039(01)87213-0
    • (1973) Tetrahedron Lett. , vol.14 , pp. 4329-4332
    • Wulff, G.1    Sarhan, A.2    Zabrocki, K.3
  • 37
    • 0015800169 scopus 로고
    • Eine Vollständige Recemattennung durch Eluitons- Chromagographie an Cellulose-tri-acetat
    • Hesse, G.; Hagel, R. Eine Vollständige Recemattennung durch Eluitons- Chromagographie an Cellulose-tri-acetat Chromatographia 1973, 6, 277-280 10.1007/BF02282825
    • (1973) Chromatographia , vol.6 , pp. 277-280
    • Hesse, G.1    Hagel, R.2
  • 38
    • 0000820691 scopus 로고
    • Resolution of DL-Tryptophan by Affinity Chromatography on Bovine-serum Albumin-agarose Columns
    • Stewart, K. K.; Doherty, R. F. Resolution of DL-Tryptophan by Affinity Chromatography on Bovine-serum Albumin-agarose Columns Proc. Natl. Acad. Sci. U. S. A. 1973, 70, 2850-2852 10.1073/pnas.70.10.2850
    • (1973) Proc. Natl. Acad. Sci. U. S. A. , vol.70 , pp. 2850-2852
    • Stewart, K.K.1    Doherty, R.F.2
  • 40
    • 0040502386 scopus 로고
    • Chromatographic Optical Resolution through Chiral Complexation of Amino Ester Salts by a Host Covalently Bound to Silica Gel
    • Dotsevi, G.; Sogah, Y.; Cram, D. J. Chromatographic Optical Resolution through Chiral Complexation of Amino Ester Salts by a Host Covalently Bound to Silica Gel J. Am. Chem. Soc. 1975, 97, 1259-1261 10.1021/ja00838a059
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 1259-1261
    • Dotsevi, G.1    Sogah, Y.2    Cram, D.J.3
  • 41
    • 84985566376 scopus 로고
    • Complete Enantiomer Separation by Chromatography on Potato Starch
    • Hess, H.; Burger, G.; Musso, H. Complete Enantiomer Separation by Chromatography on Potato Starch Angew. Chem., Int. Ed. Engl. 1978, 17, 612-614 10.1002/anie.197806121
    • (1978) Angew. Chem., Int. Ed. Engl. , vol.17 , pp. 612-614
    • Hess, H.1    Burger, G.2    Musso, H.3
  • 42
    • 0017910481 scopus 로고
    • Optical Resolution of Mandelic Acid Derivatives by Column Chromatography on Crosslinked Cyclodextrin Gels
    • Harada, A.; Furue, M.; Nozakura, S. Optical Resolution of Mandelic Acid Derivatives by Column Chromatography on Crosslinked Cyclodextrin Gels J. Polym. Sci., Polym. Chem. Ed. 1978, 16, 189-196 10.1002/pol.1978.170160119
    • (1978) J. Polym. Sci., Polym. Chem. Ed. , vol.16 , pp. 189-196
    • Harada, A.1    Furue, M.2    Nozakura, S.3
  • 43
    • 0001497432 scopus 로고
    • Chiral High-pressure Liquid Chromatographic Stationary Phases. 1. Separation of the Enantiomers of Sulfoxides, Amines, Amino Acids, Alcohols, Hydroxy Acids, Lactones, and Mercaptans
    • Pirkle, W. H.; House, D. W. Chiral High-pressure Liquid Chromatographic Stationary Phases. 1. Separation of the Enantiomers of Sulfoxides, Amines, Amino Acids, Alcohols, Hydroxy Acids, Lactones, and Mercaptans J. Org. Chem. 1979, 44, 1957-1960 10.1021/jo01326a014
    • (1979) J. Org. Chem. , vol.44 , pp. 1957-1960
    • Pirkle, W.H.1    House, D.W.2
  • 44
    • 33845560736 scopus 로고
    • Optically Active Poly(triphenylmethyl methacrylate) with One-handed Helical Conformation
    • Okamoto, Y.; Suzuki, K.; Ohta, K.; Hatada, K.; Yuki, H. Optically Active Poly(triphenylmethyl methacrylate) with One-handed Helical Conformation J. Am. Chem. Soc. 1979, 101, 4763-4765 10.1021/ja00510a072
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 4763-4765
    • Okamoto, Y.1    Suzuki, K.2    Ohta, K.3    Hatada, K.4    Yuki, H.5
  • 45
    • 0000333083 scopus 로고
    • Resolution of Racemic Compounds by Optically Active Poly(triphenylmethyl methacrylate)
    • Yuki, H.; Okamoto, Y.; Okamoto, I. Resolution of Racemic Compounds by Optically Active Poly(triphenylmethyl methacrylate) J. Am. Chem. Soc. 1980, 102, 6356-6358 10.1021/ja00540a039
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 6356-6358
    • Yuki, H.1    Okamoto, Y.2    Okamoto, I.3
  • 46
    • 0001570050 scopus 로고
    • Novel Packing Material for Optical Resolution: (+)-Poly(triphenylmethyl Methacrylate) Coated on Macroporous Silica Gel
    • Okamoto, Y.; Honda, S.; Okamoto, I.; Yuki, H.; Murata, S.; Noyori, R.; Takaya, H. Novel Packing Material for Optical Resolution: (+)-Poly(triphenylmethyl Methacrylate) Coated on Macroporous Silica Gel J. Am. Chem. Soc. 1981, 103, 6971-6973 10.1021/ja00413a038
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 6971-6973
    • Okamoto, Y.1    Honda, S.2    Okamoto, I.3    Yuki, H.4    Murata, S.5    Noyori, R.6    Takaya, H.7
  • 47
    • 0001126895 scopus 로고
    • Optical Resolution of Atropisomeric Poly(triphenylmethyl methacrylate)
    • Okamoto, Y.; Honda, S.; Okamoto, I.; Yuki, H. Optical Resolution of Atropisomeric Poly(triphenylmethyl methacrylate) J. Polym. Sci., Polym. Lett. Ed. 1981, 19, 451-455 10.1002/pol.1981.130190904
    • (1981) J. Polym. Sci., Polym. Lett. Ed. , vol.19 , pp. 451-455
    • Okamoto, Y.1    Honda, S.2    Okamoto, I.3    Yuki, H.4
  • 48
    • 0019525285 scopus 로고
    • Separation of Isotactic Polymers of (R)-(+)- and (S)-(-)- α-Methylbenzyl Methacrylates on Opticlly Active Polychloral
    • Hatada, H.; Shimizu, S.; Yuki, H.; Harria, W.; Vogl, O. Separation of Isotactic Polymers of (R)-(+)- and (S)-(-)- α-Methylbenzyl Methacrylates on Opticlly Active Polychloral Polym. Bull. 1981, 4, 179-183 10.1007/BF00263059
    • (1981) Polym. Bull. , vol.4 , pp. 179-183
    • Hatada, H.1    Shimizu, S.2    Yuki, H.3    Harria, W.4    Vogl, O.5
  • 49
    • 0001151298 scopus 로고
    • A Widely Useful Chiral Stationary Phase for the High-Performance Liquid Chromatography Separation of Enantiomers
    • Pirkle, W. H.; Finn, J. M.; Schreiner, J. L.; Hamper, B. C. A Widely Useful Chiral Stationary Phase for the High-Performance Liquid Chromatography Separation of Enantiomers J. Am. Chem. Soc. 1981, 103, 3964-3966 10.1021/ja00403a076
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 3964-3966
    • Pirkle, W.H.1    Finn, J.M.2    Schreiner, J.L.3    Hamper, B.C.4
  • 50
    • 4544277916 scopus 로고    scopus 로고
    • (-)-Sparteine: the Compound that Most Significantly Influenced My Research
    • Okamoto, Y. (-)-Sparteine: The Compound that Most Significantly Influenced My Research J. Polym. Sci., Part A: Polym. Chem. 2004, 42, 4480-4491 10.1002/pola.20192
    • (2004) J. Polym. Sci., Part A: Polym. Chem. , vol.42 , pp. 4480-4491
    • Okamoto, Y.1
  • 51
    • 0000915204 scopus 로고
    • Useful Chiral Packing Materials for High-Performance Liquid Chromatographic Resolution. Cellulose Triacetate and Tribenzoate Coated on Macroporous Silica Gel
    • Okamoto, Y.; Kawashima, M.; Yamamoto, K.; Hatada, K. Useful Chiral Packing Materials for High-Performance Liquid Chromatographic Resolution. Cellulose Triacetate and Tribenzoate Coated on Macroporous Silica Gel Chem. Lett. 1984, 13, 739-742 10.1246/cl.1984.739
    • (1984) Chem. Lett. , vol.13 , pp. 739-742
    • Okamoto, Y.1    Kawashima, M.2    Yamamoto, K.3    Hatada, K.4
  • 52
    • 0012003562 scopus 로고
    • Useful Chiral Packing Materials for High-Performance Liquid Chromatographic Resolution of Enantiomers: Phenylcarbamates of Polysaccharides Coated on Silica Gel
    • Okamoto, Y.; Kawashima, M.; Hatada, K. Useful Chiral Packing Materials for High-Performance Liquid Chromatographic Resolution of Enantiomers: Phenylcarbamates of Polysaccharides Coated on Silica Gel J. Am. Chem. Soc. 1984, 106, 5357-5359 10.1021/ja00330a057
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 5357-5359
    • Okamoto, Y.1    Kawashima, M.2    Hatada, K.3
  • 54
    • 0021491345 scopus 로고
    • Cyclodextrin Bonded Phases for the Liquid-Chromatographic Separation of Optical, Geometrical, and Structural Isomers
    • Armstrong, D.; DeMond, W. Cyclodextrin Bonded Phases for the Liquid-Chromatographic Separation of Optical, Geometrical, and Structural Isomers J. Chromatogr. Sci. 1984, 22, 411-415 10.1093/chromsci/22.9.411
    • (1984) J. Chromatogr. Sci. , vol.22 , pp. 411-415
    • Armstrong, D.1    Demond, W.2
  • 55
    • 0038559960 scopus 로고
    • New Chiral Stationary Phases for Optical Resolution. Optically Active Polyamides Having (-)-Anti Head-to-head Coumarin Dimer Component
    • Saigo, K.; Chen, Y.; Yonezawa, N.; Tachibana, K.; Kanoe, T.; Hasegawa, M. New Chiral Stationary Phases for Optical Resolution. Optically Active Polyamides Having (-)-Anti Head-to-head Coumarin Dimer Component Chem. Lett. 1985, 14, 1891-1894 10.1246/cl.1985.1891
    • (1985) Chem. Lett. , vol.14 , pp. 1891-1894
    • Saigo, K.1    Chen, Y.2    Yonezawa, N.3    Tachibana, K.4    Kanoe, T.5    Hasegawa, M.6
  • 56
    • 0002642210 scopus 로고
    • Controlled Chiral Recognition of Cellulose Triphenylcarbamate Derivatives Supported on Silica Gel
    • Okamoto, Y.; Kawashima, M.; Hatada, K. Controlled Chiral Recognition of Cellulose Triphenylcarbamate Derivatives Supported on Silica Gel J. Chromatogr. 1986, 363, 173-186 10.1016/S0021-9673(01)83736-5
    • (1986) J. Chromatogr. , vol.363 , pp. 173-186
    • Okamoto, Y.1    Kawashima, M.2    Hatada, K.3
  • 57
    • 0002640343 scopus 로고
    • Useful Chiral Stationary Phases for HPLC. Amylose Tris(3,5-dimethylphenylcarbamate) and Tris(3,5-dichlorophenylcarbamate) Supported on Silica Gel
    • Okamoto, Y.; Aburatani, R.; Fukumoto, T.; Hatada, K. Useful Chiral Stationary Phases for HPLC. Amylose Tris(3,5-dimethylphenylcarbamate) and Tris(3,5-dichlorophenylcarbamate) Supported on Silica Gel Chem. Lett. 1987, 16, 1857-1860 10.1246/cl.1987.1857
    • (1987) Chem. Lett. , vol.16 , pp. 1857-1860
    • Okamoto, Y.1    Aburatani, R.2    Fukumoto, T.3    Hatada, K.4
  • 58
    • 0023175366 scopus 로고
    • Chiral Stationary Phases for HPLC: Cellulose Tris(3,5-dimethylphenylcarbamate) and Tris(3,5-dichlorophenylcarbamate) Chemically Bonded to Silica Gel
    • Okamoto, Y.; Aburatani, R.; Miura, S.; Hatada, K. Chiral Stationary Phases for HPLC: Cellulose Tris(3,5-dimethylphenylcarbamate) and Tris(3,5-dichlorophenylcarbamate) Chemically Bonded to Silica Gel J. Liq. Chromatogr. 1987, 10, 1613-1628 10.1080/01483918708066791
    • (1987) J. Liq. Chromatogr. , vol.10 , pp. 1613-1628
    • Okamoto, Y.1    Aburatani, R.2    Miura, S.3    Hatada, K.4
  • 59
    • 19344376760 scopus 로고    scopus 로고
    • Solvent Versatility of Immobilized 3,5-Dimethylphenylcarbamate of Amylose in Enantiomeric Separations by HPLC
    • Zhang, T.; Kientzy, C.; Franco, P.; Ohnishi, A.; Kagamihara, Y.; Kurosawa, H. Solvent Versatility of Immobilized 3,5-Dimethylphenylcarbamate of Amylose in Enantiomeric Separations by HPLC J. Chromatogr. A 2005, 1075, 65-75 10.1016/j.chroma.2005.03.116
    • (2005) J. Chromatogr. A , vol.1075 , pp. 65-75
    • Zhang, T.1    Kientzy, C.2    Franco, P.3    Ohnishi, A.4    Kagamihara, Y.5    Kurosawa, H.6
  • 60
    • 85042810334 scopus 로고    scopus 로고
    • PCT International Patent Application
    • Francotte, E.; Zhang, T. PCT International Patent Application WO 9704011, 1996.
    • (1996)
    • Francotte, E.1    Zhang, T.2
  • 61
    • 85031962433 scopus 로고    scopus 로고
    • Chem. Abstr. 1997, 126, 213598
    • (1997) Chem. Abstr. , vol.126 , pp. 213598
  • 62
    • 0028227322 scopus 로고
    • Macrocyclic Antibiotics as a New Class of Chiral Selectors for Liquid Chromatography
    • Armstrong, D. W.; Tang, Y.; Chen, S.; Zhou, Y.; Bagwill, C.; Chen, J. R. Macrocyclic Antibiotics as a New Class of Chiral Selectors for Liquid Chromatography Anal. Chem. 1994, 66, 1473-1484 10.1021/ac00081a019
    • (1994) Anal. Chem. , vol.66 , pp. 1473-1484
    • Armstrong, D.W.1    Tang, Y.2    Chen, S.3    Zhou, Y.4    Bagwill, C.5    Chen, J.R.6
  • 63
    • 37049070491 scopus 로고
    • An Optically Active Stereoregular Polyphenylacetylene Derivative as a Novel Chiral Stationary Phase for HPLC
    • Yashima, E.; Huang, S.; Okamoto, Y. An Optically Active Stereoregular Polyphenylacetylene Derivative as a Novel Chiral Stationary Phase for HPLC J. Chem. Soc., Chem. Commun. 1994, 1811-1812 10.1039/c39940001811
    • (1994) J. Chem. Soc., Chem. Commun. , pp. 1811-1812
    • Yashima, E.1    Huang, S.2    Okamoto, Y.3
  • 64
    • 0028847071 scopus 로고
    • A New Class of Network-Polymeric Chiral Stationary Phases
    • Allenmark, S. G.; Andersson, S.; Möller, P.; Sanchez, D. A New Class of Network-Polymeric Chiral Stationary Phases Chirality 1995, 7, 248-256 10.1002/chir.530070411
    • (1995) Chirality , vol.7 , pp. 248-256
    • Allenmark, S.G.1    Andersson, S.2    Möller, P.3    Sanchez, D.4
  • 65
    • 0030576524 scopus 로고    scopus 로고
    • Quinine and Quinidine Derivatives as Chiral Selectors I. Brush Type Chiral Stationary Phases for High-Performance Liquid Chromatography Based on Cinchonan Carbamates and Their Application as Chiral Anion Exchangers
    • Lämmerhofer, M.; Lindner, W. Quinine and Quinidine Derivatives as Chiral Selectors I. Brush Type Chiral Stationary Phases for High-Performance Liquid Chromatography Based on Cinchonan Carbamates and Their Application as Chiral Anion Exchangers J. Chromatogr. A 1996, 741, 33-48 10.1016/0021-9673(96)00137-9
    • (1996) J. Chromatogr. A , vol.741 , pp. 33-48
    • Lämmerhofer, M.1    Lindner, W.2
  • 66
    • 0036194086 scopus 로고    scopus 로고
    • Asymmetric Polymerization of N-1-Anthrylmaleimide with Diethylzinc-Chiral Ligand Complexes and Optical Resolution Using the Polymer
    • Isobe, Y.; Onimura, K.; Tsutsumi, H.; Oishi, T. Asymmetric Polymerization of N-1-Anthrylmaleimide with Diethylzinc-Chiral Ligand Complexes and Optical Resolution Using the Polymer Polym. J. 2002, 34, 18-24 10.1295/polymj.34.18
    • (2002) Polym. J. , vol.34 , pp. 18-24
    • Isobe, Y.1    Onimura, K.2    Tsutsumi, H.3    Oishi, T.4
  • 67
    • 72449121300 scopus 로고    scopus 로고
    • Development of New HPLC Chiral Stationary Phases Based on Native and Derivatized Cyclofructants
    • Sun, P.; Wang, C.; Breitbach, Z. S.; Zhang, Y.; Armstrong, D. Development of New HPLC Chiral Stationary Phases Based on Native and Derivatized Cyclofructants Anal. Chem. 2009, 81, 10215-10226 10.1021/ac902257a
    • (2009) Anal. Chem. , vol.81 , pp. 10215-10226
    • Sun, P.1    Wang, C.2    Breitbach, Z.S.3    Zhang, Y.4    Armstrong, D.5
  • 68
    • 0000936090 scopus 로고
    • Resolution into Optical Isomers of Some Amino Acids by Paper Chromatography
    • Kotake, M.; Sakan, T.; Nakamura, N.; Senoh, S. Resolution into Optical Isomers of Some Amino Acids by Paper Chromatography J. Am. Chem. Soc. 1951, 73, 2973-2974 10.1021/ja01150a548
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 2973-2974
    • Kotake, M.1    Sakan, T.2    Nakamura, N.3    Senoh, S.4
  • 69
    • 39149140764 scopus 로고
    • Separation of Enantiomers by Gas Liquid Chromatography with an Optically Active Stationary Phase
    • Gil-Av, E.; Feibush, B.; Charles-Sigler, R. Separation of Enantiomers by Gas Liquid Chromatography with an Optically Active Stationary Phase Tetrahedron Lett. 1966, 7, 1009-1015 10.1016/S0040-4039(00)70231-0
    • (1966) Tetrahedron Lett. , vol.7 , pp. 1009-1015
    • Gil-Av, E.1    Feibush, B.2    Charles-Sigler, R.3
  • 70
    • 0017495101 scopus 로고
    • Rapid Gas-Chromatographic Separation of Amino-acid Enantiomers with a Novel Chiral Stationary Phase
    • Frank, H.; Nicholson, G. J.; Bayer, E. Rapid Gas-Chromatographic Separation of Amino-acid Enantiomers with a Novel Chiral Stationary Phase J. Chromatogr. Sci. 1977, 15, 174-176 10.1093/chromsci/15.5.174
    • (1977) J. Chromatogr. Sci. , vol.15 , pp. 174-176
    • Frank, H.1    Nicholson, G.J.2    Bayer, E.3
  • 71
    • 0022161544 scopus 로고
    • Electrokinetic Separation of Chiral Compounds
    • Gassmann, E.; Kuo, J. E.; Zaew, R. N. Electrokinetic Separation of Chiral Compounds Science 1985, 230, 813-814 10.1126/science.230.4727.813
    • (1985) Science , vol.230 , pp. 813-814
    • Gassmann, E.1    Kuo, J.E.2    Zaew, R.N.3
  • 72
    • 0000719583 scopus 로고
    • Supercritical and Subcritical Fluid Chromatography on a Chiral Stationary Phase for the Resolution of Phosphine Oxide Enantiomers
    • Mourier, P. A.; Eliot, E.; Caude, M. H.; Rosset, R. H.; Tambute, A. G. Supercritical and Subcritical Fluid Chromatography on a Chiral Stationary Phase for the Resolution of Phosphine Oxide Enantiomers Anal. Chem. 1985, 57, 2819-2823 10.1021/ac00291a017
    • (1985) Anal. Chem. , vol.57 , pp. 2819-2823
    • Mourier, P.A.1    Eliot, E.2    Caude, M.H.3    Rosset, R.H.4    Tambute, A.G.5
  • 73
    • 0001490117 scopus 로고
    • Separation of Enantiomers on Diluted Permethylated β-Cyclodextrin by High-Resolution Gas Chromatography
    • Schurig, V.; Nowotny, H.-P. Separation of Enantiomers on Diluted Permethylated β-Cyclodextrin by High-Resolution Gas Chromatography J. Chromatogr. 1988, 441, 155-163 10.1016/S0021-9673(01)84662-8
    • (1988) J. Chromatogr. , vol.441 , pp. 155-163
    • Schurig, V.1    Nowotny, H.-P.2
  • 74
    • 0000686172 scopus 로고
    • Cyclodextrins as Chiral Stationary Phases in Capillary Gas Chromatography. I. Pentylated α-Cyclodexitrin
    • König, W. A.; Lutz, S.; Mischnick-Lübbecke, P.; Brassat, B. Cyclodextrins as Chiral Stationary Phases in Capillary Gas Chromatography. I. Pentylated α-Cyclodexitrin J. Chromatogr. 1988, 447, 193-197 10.1016/0021-9673(88)90020-9
    • (1988) J. Chromatogr. , vol.447 , pp. 193-197
    • König, W.A.1    Lutz, S.2    Mischnick-Lübbecke, P.3    Brassat, B.4
  • 75
    • 0025421333 scopus 로고
    • Enantioselective Permeation of α-Amino Acid Isomers through Poly(amino acid)-Derived Membranes
    • Maruyama, A.; Adachi, N.; Takatsuki, T.; Torii, M.; Sanui, K.; Ogata, N. Enantioselective Permeation of α-Amino Acid Isomers through Poly(amino acid)-Derived Membranes Macromolecules 1990, 23, 2748-2752 10.1021/ma00212a027
    • (1990) Macromolecules , vol.23 , pp. 2748-2752
    • Maruyama, A.1    Adachi, N.2    Takatsuki, T.3    Torii, M.4    Sanui, K.5    Ogata, N.6
  • 76
    • 0001399210 scopus 로고
    • Optical Resolution through the Solid Membrane from (+)-Poly(1-[dimethyl(10-pinanyl)silyl]-1-propyne)
    • Aoki, T.; Shinohara, K.; Oikawa, E. Optical Resolution through the Solid Membrane from (+)-Poly(1-[dimethyl(10-pinanyl)silyl]-1-propyne) Makromol. Chem., Rapid Commun. 1992, 13, 565-570 10.1002/marc.1992.030131206
    • (1992) Makromol. Chem., Rapid Commun. , vol.13 , pp. 565-570
    • Aoki, T.1    Shinohara, K.2    Oikawa, E.3
  • 77
    • 84985200124 scopus 로고
    • Enantiomer Separation by Electrochromatography on Capillaries Coated with Chirasil-Dex
    • Mayer, S.; Schurig, V. Enantiomer Separation by Electrochromatography on Capillaries Coated with Chirasil-Dex J. High Resolut. Chromatogr. 1992, 15, 129-131 10.1002/jhrc.1240150216
    • (1992) J. High Resolut. Chromatogr. , vol.15 , pp. 129-131
    • Mayer, S.1    Schurig, V.2
  • 78
    • 0001947093 scopus 로고
    • Chromatographic Resolution of Racemates
    • Blaschke, G. Chromatographic Resolution of Racemates Angew. Chem., Int. Ed. Engl. 1980, 19, 13-24 10.1002/anie.198000131
    • (1980) Angew. Chem., Int. Ed. Engl. , vol.19 , pp. 13-24
    • Blaschke, G.1
  • 79
    • 84985574704 scopus 로고
    • Enantiomeric Resolution by HPLC on Silica-Gel-Bound, Optically Active Polyamides
    • Blaschke, G.; Bröeker, W.; Frankel, W. Enantiomeric Resolution by HPLC on Silica-Gel-Bound, Optically Active Polyamides Angew. Chem., Int. Ed. Engl. 1986, 25, 830-831 10.1002/anie.198608301
    • (1986) Angew. Chem., Int. Ed. Engl. , vol.25 , pp. 830-831
    • Blaschke, G.1    Bröeker, W.2    Frankel, W.3
  • 80
    • 0022624282 scopus 로고
    • Chromatographic Resolution of Chiral Drugs on Polyamides and Cellulose Triacetate
    • Blaschke, G. Chromatographic Resolution of Chiral Drugs on Polyamides and Cellulose Triacetate J. Liq. Chromatogr. 1986, 9, 341-368 10.1080/01483918608076641
    • (1986) J. Liq. Chromatogr. , vol.9 , pp. 341-368
    • Blaschke, G.1
  • 81
    • 0018620980 scopus 로고
    • Chromatographische Racemattrennung von Thalidomid und Teratogene Wirkung der Enantiomere
    • Blaschke, G.; Kraft, H.-P.; Fickentscher, K.; Köhler, F. Chromatographische Racemattrennung von Thalidomid und Teratogene Wirkung der Enantiomere Arzneim. Forsch. 1979, 29, 1640-1642
    • (1979) Arzneim. Forsch. , vol.29 , pp. 1640-1642
    • Blaschke, G.1    Kraft, H.-P.2    Fickentscher, K.3    Köhler, F.4
  • 82
    • 0034827510 scopus 로고    scopus 로고
    • Efficient Lewis Acid-Catalyzed Stereocontrolled Radical Polymerization of Acrylamides
    • Isobe, Y.; Fujioka, D.; Habaue, S.; Okamoto, Y. Efficient Lewis Acid-Catalyzed Stereocontrolled Radical Polymerization of Acrylamides J. Am. Chem. Soc. 2001, 123, 7180-7181 10.1021/ja015888l
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 7180-7181
    • Isobe, Y.1    Fujioka, D.2    Habaue, S.3    Okamoto, Y.4
  • 83
    • 0037100199 scopus 로고    scopus 로고
    • Isotactic-Specific Radical Polymerization of Methacrylamides in the Presence of Lewis Acids
    • Suito, Y.; Isobe, Y.; Habaue, S.; Okamoto, Y. Isotactic-Specific Radical Polymerization of Methacrylamides in the Presence of Lewis Acids J. Polym. Sci., Part A: Polym. Chem. 2002, 40, 2496-2500 10.1002/pola.10337
    • (2002) J. Polym. Sci., Part A: Polym. Chem. , vol.40 , pp. 2496-2500
    • Suito, Y.1    Isobe, Y.2    Habaue, S.3    Okamoto, Y.4
  • 84
    • 0036321982 scopus 로고    scopus 로고
    • Stereocontrol in Radical Polymerization of Acrylic Monomers
    • Okamoto, Y.; Habaue, S.; Isobe, Y.; Nakano, T. Stereocontrol in Radical Polymerization of Acrylic Monomers Macromol. Symp. 2002, 183, 83-88 10.1002/1521-3900(200207)183:183::AID-MASY833.0.CO;2-K
    • (2002) Macromol. Symp. , vol.183 , pp. 83-88
    • Okamoto, Y.1    Habaue, S.2    Isobe, Y.3    Nakano, T.4
  • 85
    • 0037037893 scopus 로고    scopus 로고
    • Stereocontrolled Radical Polymerization of Acrylamides and Methacrylamides Using Lewis Acids
    • Habaue, S.; Isobe, Y.; Okamoto, Y. Stereocontrolled Radical Polymerization of Acrylamides and Methacrylamides Using Lewis Acids Tetrahedron 2002, 58, 8205-8209 10.1016/S0040-4020(02)00969-9
    • (2002) Tetrahedron , vol.58 , pp. 8205-8209
    • Habaue, S.1    Isobe, Y.2    Okamoto, Y.3
  • 86
    • 73249149857 scopus 로고    scopus 로고
    • Stereospecific Living Radical Polymerization: Dual Control of Chain Length and Tacticity for Precision Polymer Synthesis
    • Satoh, K.; Kamigaito, M. Stereospecific Living Radical Polymerization: Dual Control of Chain Length and Tacticity for Precision Polymer Synthesis Chem. Rev. 2009, 109, 5120-5156 10.1021/cr900115u
    • (2009) Chem. Rev. , vol.109 , pp. 5120-5156
    • Satoh, K.1    Kamigaito, M.2
  • 87
    • 0142138841 scopus 로고    scopus 로고
    • Synthesis and Chiral Recognition Ability of Optically Active Poly{N-[(R)-α-methoxycarbonylbenzyl]methacrylamide} with Various Tacticities by Radical Polymerization Using Lewis Acids
    • Morioka, K.; Suito, Y.; Isobe, Y.; Habaue, S.; Okamoto, Y. Synthesis and Chiral Recognition Ability of Optically Active Poly{N-[(R)-α-methoxycarbonylbenzyl]methacrylamide} with Various Tacticities by Radical Polymerization Using Lewis Acids J. Polym. Sci., Part A: Polym. Chem. 2003, 41, 3354-3360 10.1002/pola.10927
    • (2003) J. Polym. Sci., Part A: Polym. Chem. , vol.41 , pp. 3354-3360
    • Morioka, K.1    Suito, Y.2    Isobe, Y.3    Habaue, S.4    Okamoto, Y.5
  • 88
    • 84879770011 scopus 로고    scopus 로고
    • Synthesis and Chiral Recognition Ability of Optically Active Poly(methacrylamide) with Side Chains
    • Bai, J. W.; Shen, X. D.; Liu, W. B.; Zhang, C. H.; Xiao, H.; Xu, X. D. Synthesis and Chiral Recognition Ability of Optically Active Poly(methacrylamide) with Side Chains Acta Polym. Sin. 2013, 4, 419-425 10.3724/SP.J.1105.2013.12392
    • (2013) Acta Polym. Sin. , vol.4 , pp. 419-425
    • Bai, J.W.1    Shen, X.D.2    Liu, W.B.3    Zhang, C.H.4    Xiao, H.5    Xu, X.D.6
  • 89
    • 19944408977 scopus 로고    scopus 로고
    • Synthesis, Chiroptical Properties, and Chiral Recognition Ability of Optically Active Polymethacrylamides Having Various Tacticities
    • Morioka, K.; Isobe, Y.; Habaue, S.; Okamoto, Y. Synthesis, Chiroptical Properties, and Chiral Recognition Ability of Optically Active Polymethacrylamides Having Various Tacticities Polym. J. 2005, 37, 299-308 10.1295/polymj.37.299
    • (2005) Polym. J. , vol.37 , pp. 299-308
    • Morioka, K.1    Isobe, Y.2    Habaue, S.3    Okamoto, Y.4
  • 90
    • 73849134642 scopus 로고    scopus 로고
    • Synthesis and Characterization of Macroporous Silica Modified with Optically Active Poly[N-(oxazolinylphenyl)acrylamide] Derivatives for Potential Application as Chiral Stationary Phases
    • Tian, Y.; Lu, W.; Che, Y.; Shen, L. B.; Jiang, L. M.; Shen, Z. Q. Synthesis and Characterization of Macroporous Silica Modified with Optically Active Poly[N-(oxazolinylphenyl)acrylamide] Derivatives for Potential Application as Chiral Stationary Phases J. Appl. Polym. Sci. 2010, 115, 999-1007 10.1002/app.31049
    • (2010) J. Appl. Polym. Sci. , vol.115 , pp. 999-1007
    • Tian, Y.1    Lu, W.2    Che, Y.3    Shen, L.B.4    Jiang, L.M.5    Shen, Z.Q.6
  • 91
    • 0347380456 scopus 로고
    • Asymmetric Polymerization of Triphenylmethyl Methacrylate by Optically Active Anionic Catalysts
    • Okamoto, Y.; Suzuki, K.; Yuki, H. Asymmetric Polymerization of Triphenylmethyl Methacrylate by Optically Active Anionic Catalysts J. Polym. Sci., Polym. Chem. Ed. 1980, 18, 3043-3051 10.1002/pol.1980.170181013
    • (1980) J. Polym. Sci., Polym. Chem. Ed. , vol.18 , pp. 3043-3051
    • Okamoto, Y.1    Suzuki, K.2    Yuki, H.3
  • 92
    • 0012386215 scopus 로고
    • Facile Syntheses of (+)- and (-)-Poly(triphenylmethyl methacrylate)s and Their Macromers
    • Okamoto, Y.; Shohi, H.; Yuki, H. Facile Syntheses of (+)- and (-)-Poly(triphenylmethyl methacrylate)s and Their Macromers J. Polym. Sci., Polym. Lett. Ed. 1983, 21, 601-607 10.1002/pol.1983.130210803
    • (1983) J. Polym. Sci., Polym. Lett. Ed. , vol.21 , pp. 601-607
    • Okamoto, Y.1    Shohi, H.2    Yuki, H.3
  • 93
    • 0001420365 scopus 로고
    • Asymmetric Polymerization of Triphenylmethyl Methacrylate Leading to a One-handed Helical Polymer: Mechanism of Polymerization
    • Nakano, T.; Okamoto, Y.; Hatada, K. Asymmetric Polymerization of Triphenylmethyl Methacrylate Leading to a One-handed Helical Polymer: Mechanism of Polymerization J. Am. Chem. Soc. 1992, 114, 1318-1329 10.1021/ja00030a030
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1318-1329
    • Nakano, T.1    Okamoto, Y.2    Hatada, K.3
  • 94
    • 84916132165 scopus 로고
    • Resolution, Absolute Configuration, and Photoracemization of Chiral Troponoid Acetals, Cyclohepta[2,1-b:2,3-b′]di[1,4]benzoxazines
    • Okamoto, Y.; Honda, S.; Yuki, H.; Nakamura, H.; Iitaka, Y.; Nozoe, T. Resolution, Absolute Configuration, and Photoracemization of Chiral Troponoid Acetals, Cyclohepta[2,1-b:2,3-b′]di[1,4]benzoxazines Chem. Lett. 1984, 1149-1152 10.1246/cl.1984.1149
    • (1984) Chem. Lett. , pp. 1149-1152
    • Okamoto, Y.1    Honda, S.2    Yuki, H.3    Nakamura, H.4    Iitaka, Y.5    Nozoe, T.6
  • 95
    • 1542356009 scopus 로고
    • Optical Resolution of Helical and Planarchiral Metacyclophanes by High Performance Liquid Chromatography on (+)-Poly(triphenylmethyl-methacrylate)
    • Meurer, K.; Aigner, A.; Vögtle, F. Optical Resolution of Helical and Planarchiral Metacyclophanes by High Performance Liquid Chromatography on (+)-Poly(triphenylmethyl-methacrylate) J. Inclusion Phenom. 1985, 3, 51-54 10.1007/BF00658861
    • (1985) J. Inclusion Phenom. , vol.3 , pp. 51-54
    • Meurer, K.1    Aigner, A.2    Vögtle, F.3
  • 96
    • 84985534844 scopus 로고
    • The First [2.1] Phane: A New Helical Molecular Skeleton
    • Duchene, K.-H.; Vögtle, F. The First [2.1] Phane: A New Helical Molecular Skeleton Angew. Chem., Int. Ed. Engl. 1985, 24, 885-886 10.1002/anie.198508851
    • (1985) Angew. Chem., Int. Ed. Engl. , vol.24 , pp. 885-886
    • Duchene, K.-H.1    Vögtle, F.2
  • 97
    • 84984177218 scopus 로고
    • Resolution, Circular Dichroism, and Absolute Configuration of 1,1′-Biazulenes
    • Tajiri, A.; Fukuda, M.; Hatano, M.; Morita, T.; Takase, K. Resolution, Circular Dichroism, and Absolute Configuration of 1,1′-Biazulenes Angew. Chem., Int. Ed. Engl. 1983, 22, 870-871 10.1002/anie.198308701
    • (1983) Angew. Chem., Int. Ed. Engl. , vol.22 , pp. 870-871
    • Tajiri, A.1    Fukuda, M.2    Hatano, M.3    Morita, T.4    Takase, K.5
  • 98
    • 0011440713 scopus 로고
    • Preparation and Structure of (R)-(-)- and (S)-(+)-2,2′-(2,2-Dimethyl-2-silapropane-1,3-diyl)-1,1′-binaphthalene
    • Noyori, R.; Sano, N.; Murata, S.; Okamoto, Y.; Yuki, H. Preparation and Structure of (R)-(-)- and (S)-(+)-2,2′-(2,2-Dimethyl-2-silapropane-1,3-diyl)-1,1′-binaphthalene Tetrahedron Lett. 1982, 23, 2969-2972 10.1016/S0040-4039(00)87508-5
    • (1982) Tetrahedron Lett. , vol.23 , pp. 2969-2972
    • Noyori, R.1    Sano, N.2    Murata, S.3    Okamoto, Y.4    Yuki, H.5
  • 99
    • 37049104321 scopus 로고
    • Liquid Chromatographic Optical Resolution of 2,2′-Spirobibenz[e]indan Derivatives and Absolute Stereochemistry as Determined by the C.D. Exciton Chirality Method
    • Harada, N.; Iwabuchi, J.; Yokota, H.; Uda, H.; Okamoto, Y.; Yuki, H.; Kawada, Y. Liquid Chromatographic Optical Resolution of 2,2′-Spirobibenz[e]indan Derivatives and Absolute Stereochemistry as Determined by the C.D. Exciton Chirality Method J. Chem. Soc., Perkin Trans. 1 1985, 1845-1848 10.1039/p19850001845
    • (1985) J. Chem. Soc., Perkin Trans. 1 , pp. 1845-1848
    • Harada, N.1    Iwabuchi, J.2    Yokota, H.3    Uda, H.4    Okamoto, Y.5    Yuki, H.6    Kawada, Y.7
  • 100
    • 0005689237 scopus 로고
    • Chromatographic Resolution of Perchlorotriphenylamine on (+)-Poly(triphenylmethyl methacrylate)
    • Okamoto, Y.; Yashima, E.; Hatada, K.; Mislow, K. Chromatographic Resolution of Perchlorotriphenylamine on (+)-Poly(triphenylmethyl methacrylate) J. Org. Chem. 1984, 49, 557-558 10.1021/jo00177a037
    • (1984) J. Org. Chem. , vol.49 , pp. 557-558
    • Okamoto, Y.1    Yashima, E.2    Hatada, K.3    Mislow, K.4
  • 101
    • 0029047285 scopus 로고
    • Resolution by Chiral HPLC of the Stable Free Radical Perchlorotriphenylmethyl: Thermodynamic and Chiroptical Properties
    • Irurre, J.; Santamaria, J.; Gonzalez-Rego, M. C. Resolution by Chiral HPLC of the Stable Free Radical Perchlorotriphenylmethyl: Thermodynamic and Chiroptical Properties Chirality 1995, 7, 154-157 10.1002/chir.530070308
    • (1995) Chirality , vol.7 , pp. 154-157
    • Irurre, J.1    Santamaria, J.2    Gonzalez-Rego, M.C.3
  • 102
    • 37049095186 scopus 로고
    • Synthesis and Chiral Recognition of Novel Crown Ethers Incorporating Helicene Chiral Centres
    • Nakazaki, M.; Koji, K.; Ikeda, T.; Kitsuki, T.; Okamoto, Y. Synthesis and Chiral Recognition of Novel Crown Ethers Incorporating Helicene Chiral Centres J. Chem. Soc., Chem. Commun. 1983, 787-788 10.1039/c39830000787
    • (1983) J. Chem. Soc., Chem. Commun. , pp. 787-788
    • Nakazaki, M.1    Koji, K.2    Ikeda, T.3    Kitsuki, T.4    Okamoto, Y.5
  • 105
    • 26644444744 scopus 로고
    • Preparation of Optically Active 1,6,12c,12d-Tetramethyl-12c,12d-dihydrocoronene with Known Absolute Configuration
    • Yamamoto, K.; Ueda, T.; Yumioka, H.; Okamoto, Y.; Yoshida, T. Preparation of Optically Active 1,6,12c,12d-Tetramethyl-12c,12d-dihydrocoronene with Known Absolute Configuration Chem. Lett. 1984, 1977-1978 10.1246/cl.1984.1977
    • (1984) Chem. Lett. , pp. 1977-1978
    • Yamamoto, K.1    Ueda, T.2    Yumioka, H.3    Okamoto, Y.4    Yoshida, T.5
  • 106
    • 84985615591 scopus 로고
    • A Three-Blade Propeller Compound with Seven Bracketed Benzene Rings
    • Kissener, W.; Vögtle, F. A Three-Blade Propeller Compound with Seven Bracketed Benzene Rings Angew. Chem., Int. Ed. Engl. 1985, 24, 222-223 10.1002/anie.198502221
    • (1985) Angew. Chem., Int. Ed. Engl. , vol.24 , pp. 222-223
    • Kissener, W.1    Vögtle, F.2
  • 107
    • 0030742710 scopus 로고    scopus 로고
    • Chemistry of Unique Chiral Olefins. 2. Unexpected Thermal Racemization of Bis-1,1′,2,2′,3,3′,4,4′-octahydro-4,4′- biphenanthrylidene
    • Harada, N.; Saito, A.; Koumura, N.; Roe, D. C.; Jager, W. F.; Zijlstra, R. W. J.; de Lange, B.; Feringa, B. L. Chemistry of Unique Chiral Olefins. 2. Unexpected Thermal Racemization of Bis-1,1′,2,2′,3,3′,4,4′-octahydro-4,4′- biphenanthrylidene J. Am. Chem. Soc. 1997, 119, 7249-7255 10.1021/ja970668m
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 7249-7255
    • Harada, N.1    Saito, A.2    Koumura, N.3    Roe, D.C.4    Jager, W.F.5    Zijlstra, R.W.J.6    De Lange, B.7    Feringa, B.L.8
  • 108
    • 37049096845 scopus 로고
    • Synthesis and Chiral Recognition of Optically Active Crown Ethers Incorporating a Biphenanthryl Moiety as the Chiral Centre
    • Yamamoto, K.; Fukushima, H.; Okamoto, Y.; Hatada, K.; Nakazaki, M. Synthesis and Chiral Recognition of Optically Active Crown Ethers Incorporating a Biphenanthryl Moiety as the Chiral Centre J. Chem. Soc., Chem. Commun. 1984, 1111-1112 10.1039/c39840001111
    • (1984) J. Chem. Soc., Chem. Commun. , pp. 1111-1112
    • Yamamoto, K.1    Fukushima, H.2    Okamoto, Y.3    Hatada, K.4    Nakazaki, M.5
  • 109
    • 0001618678 scopus 로고
    • Resolution and Enantiomerization Barrier of Tetramesitylethylene
    • Gur, E.; Kaida, Y.; Okamoto, Y.; Biali, S.; Rappoport, Z. Resolution and Enantiomerization Barrier of Tetramesitylethylene J. Org. Chem. 1992, 57, 3689-3693 10.1021/jo00039a033
    • (1992) J. Org. Chem. , vol.57 , pp. 3689-3693
    • Gur, E.1    Kaida, Y.2    Okamoto, Y.3    Biali, S.4    Rappoport, Z.5
  • 110
    • 0011546936 scopus 로고
    • Stereoisomerism in Molecular Bevel-gears. Optical Resolution of the DL Isomers of Bis(2- and 3-chloro-9-triptycyl)methanes and Ethers
    • Kawada, Y.; Iwamura, H.; Okamoto, Y.; Yuki, H. Stereoisomerism in Molecular Bevel-gears. Optical Resolution of the DL Isomers of Bis(2- and 3-chloro-9-triptycyl)methanes and Ethers Tetrahedron Lett. 1983, 24, 791-794 10.1016/S0040-4039(00)81529-4
    • (1983) Tetrahedron Lett. , vol.24 , pp. 791-794
    • Kawada, Y.1    Iwamura, H.2    Okamoto, Y.3    Yuki, H.4
  • 111
    • 0001190057 scopus 로고
    • Correlated Internal Rotation in Bis(2,6-dichloro-9-triptycyl)methane. to What Extent Can Phase Isomers Be Separated and Identified?
    • Kawada, Y.; Okamoto, Y.; Iwamura, H. Correlated Internal Rotation in Bis(2,6-dichloro-9-triptycyl)methane. To What Extent Can Phase Isomers Be Separated and Identified? Tetrahedron Lett. 1983, 24, 5359-5362 10.1016/S0040-4039(00)87868-5
    • (1983) Tetrahedron Lett. , vol.24 , pp. 5359-5362
    • Kawada, Y.1    Okamoto, Y.2    Iwamura, H.3
  • 112
    • 84963176508 scopus 로고
    • Resolution of Enantiomers by HPLC on Optically Active Poly(triphenylmethyl methacrylate)
    • Okamoto, Y.; Hatada, K. Resolution of Enantiomers by HPLC on Optically Active Poly(triphenylmethyl methacrylate) J. Liq. Chromatogr. 1986, 9, 369-384 10.1080/01483918608076642
    • (1986) J. Liq. Chromatogr. , vol.9 , pp. 369-384
    • Okamoto, Y.1    Hatada, K.2
  • 113
    • 85016536038 scopus 로고
    • Preparation of Optically Active Poly(triphenylmethyl methacrylate) Chemically Bonded to Silica Gel and Its Application for Optical Resolution by HPLC
    • Okamoto, Y.; Mohri, H.; Nakamura, M.; Hatada, K. Preparation of Optically Active Poly(triphenylmethyl methacrylate) Chemically Bonded to Silica Gel and Its Application for Optical Resolution by HPLC Nippon Kagaku Kaishi 1987, 435-440 10.1246/nikkashi.1987.435
    • (1987) Nippon Kagaku Kaishi , pp. 435-440
    • Okamoto, Y.1    Mohri, H.2    Nakamura, M.3    Hatada, K.4
  • 114
    • 84966198108 scopus 로고
    • Stereospecific and Asymmetric Polymerization of Diphenylpyridylmethyl Methacrylates
    • Okamoto, Y.; Ishikura, H.; Hatada, K.; Yuki, H. Stereospecific and Asymmetric Polymerization of Diphenylpyridylmethyl Methacrylates Polym. J. 1983, 15, 851-853 10.1295/polymj.15.851
    • (1983) Polym. J. , vol.15 , pp. 851-853
    • Okamoto, Y.1    Ishikura, H.2    Hatada, K.3    Yuki, H.4
  • 115
    • 0002875035 scopus 로고
    • Highly Helix-Sense-Selective Polymerization of Diphenyl-2-pyridylmethyl Methacrylate
    • Okamoto, Y.; Mohri, H.; Hatada, K. Highly Helix-Sense-Selective Polymerization of Diphenyl-2-pyridylmethyl Methacrylate Chem. Lett. 1988, 1879-1882 10.1246/cl.1988.1879
    • (1988) Chem. Lett. , pp. 1879-1882
    • Okamoto, Y.1    Mohri, H.2    Hatada, K.3
  • 116
    • 0025988504 scopus 로고
    • Helix-Sense-Selective Polymerization of Diphenyl-2-pyridylmethyl Methacrylate with Chiral Anionic Initiators
    • Okamoto, Y.; Mohri, H.; Nakano, T.; Hatada, K. Helix-Sense-Selective Polymerization of Diphenyl-2-pyridylmethyl Methacrylate with Chiral Anionic Initiators Chirality 1991, 3, 277-284 10.1002/chir.530030411
    • (1991) Chirality , vol.3 , pp. 277-284
    • Okamoto, Y.1    Mohri, H.2    Nakano, T.3    Hatada, K.4
  • 117
    • 0024858911 scopus 로고
    • Chromatographic Optical Resolution by Optically Active Poly(diphenyl-2-pyridylmethyl methacrylate) with a Highly One-handed Helical Structure
    • Okamoto, Y.; Mohri, H.; Hatada, K. Chromatographic Optical Resolution by Optically Active Poly(diphenyl-2-pyridylmethyl methacrylate) with a Highly One-handed Helical Structure Polym. J. 1989, 21, 439-445 10.1295/polymj.21.439
    • (1989) Polym. J. , vol.21 , pp. 439-445
    • Okamoto, Y.1    Mohri, H.2    Hatada, K.3
  • 118
    • 84924535350 scopus 로고    scopus 로고
    • Direct Separation of the Diastereomers of Phosphatidylcholine Hydroperoxide Bearing 13-Hydroperoxy-9Z,11E-octadecadienoic Acid Using Chiral Stationary Phase High-Performance Liquid Chromatography
    • Ito, J.; Nakagawa, K.; Kato, S.; Hirokawa, T.; Kuwahara, S.; Nagai, T.; Miyazawa, T. Direct Separation of the Diastereomers of Phosphatidylcholine Hydroperoxide Bearing 13-Hydroperoxy-9Z,11E-octadecadienoic Acid Using Chiral Stationary Phase High-Performance Liquid Chromatography J. Chromatogr. A 2015, 1386, 53-61 10.1016/j.chroma.2015.01.080
    • (2015) J. Chromatogr. A , vol.1386 , pp. 53-61
    • Ito, J.1    Nakagawa, K.2    Kato, S.3    Hirokawa, T.4    Kuwahara, S.5    Nagai, T.6    Miyazawa, T.7
  • 119
    • 0027678238 scopus 로고
    • Helix-Sense-Selective Polymerization of Phenyl[bis(2-pyridyl)]methyl Methacrylate and Chiral Recognition Ability of the Polymer
    • Ren, C.; Chen, C.; Xi, F.; Nakano, T.; Okamoto, Y. Helix-Sense-Selective Polymerization of Phenyl[bis(2-pyridyl)]methyl Methacrylate and Chiral Recognition Ability of the Polymer J. Polym. Sci., Part A: Polym. Chem. 1993, 31, 2721-2728 10.1002/pola.1993.080311107
    • (1993) J. Polym. Sci., Part A: Polym. Chem. , vol.31 , pp. 2721-2728
    • Ren, C.1    Chen, C.2    Xi, F.3    Nakano, T.4    Okamoto, Y.5
  • 120
    • 0023565929 scopus 로고
    • Synthesis, Methanolysis, and Asymmetric Polymerization of meta- and para-Substituted Triphenylmethyl Methacrylates
    • Okamoto, Y.; Yashima, E.; Ishikura, M.; Hatada, K. Synthesis, Methanolysis, and Asymmetric Polymerization of meta- and para-Substituted Triphenylmethyl Methacrylates Polym. J. 1987, 19, 1183-1190 10.1295/polymj.19.1183
    • (1987) Polym. J. , vol.19 , pp. 1183-1190
    • Okamoto, Y.1    Yashima, E.2    Ishikura, M.3    Hatada, K.4
  • 121
    • 0029699267 scopus 로고    scopus 로고
    • Asymmetric Anionic Polymerization of 1-Phenyldibenzosuberyl and 1-(2-Pyridyl)dibenzosuberyl Methacrylates and Chiral Recognition Ability of the Obtained Polymers
    • Nakano, T.; Matsuda, A.; Mori, M.; Okamoto, Y. Asymmetric Anionic Polymerization of 1-Phenyldibenzosuberyl and 1-(2-Pyridyl)dibenzosuberyl Methacrylates and Chiral Recognition Ability of the Obtained Polymers Polym. J. 1996, 28, 330-336 10.1295/polymj.28.330
    • (1996) Polym. J. , vol.28 , pp. 330-336
    • Nakano, T.1    Matsuda, A.2    Mori, M.3    Okamoto, Y.4
  • 122
    • 0031631631 scopus 로고    scopus 로고
    • Asymmetric Polymerization of 1-(3-Pyridyl)dibenzosuberyl Methacrylate and Chiral Recognition by the Obtained Optically Active Polymer Having Single-Handed Helical Conformation
    • Nakano, T.; Sato, Y.; Okamoto, Y. Asymmetric Polymerization of 1-(3-Pyridyl)dibenzosuberyl Methacrylate and Chiral Recognition by the Obtained Optically Active Polymer Having Single-Handed Helical Conformation Polym. J. 1998, 30, 635-640 10.1295/polymj.30.635
    • (1998) Polym. J. , vol.30 , pp. 635-640
    • Nakano, T.1    Sato, Y.2    Okamoto, Y.3
  • 123
    • 77955321826 scopus 로고    scopus 로고
    • A Reactive Helix: Synthesis, Chemical Modification, and Polymerization of an Optically Active Polymethacrylate
    • Sakamoto, T.; Nishikawa, T.; Fukuda, Y.; Sato, S.-I.; Nakano, T. A Reactive Helix: Synthesis, Chemical Modification, and Polymerization of an Optically Active Polymethacrylate Macromolecules 2010, 43, 5956-5963 10.1021/ma101057j
    • (2010) Macromolecules , vol.43 , pp. 5956-5963
    • Sakamoto, T.1    Nishikawa, T.2    Fukuda, Y.3    Sato, S.-I.4    Nakano, T.5
  • 124
    • 0019604882 scopus 로고
    • Structural Change of st-PMMA on Drawing, Absorption and Desorption of Solvents
    • Kusuyama, H.; Takase, M.; Higashiyama, Y.; Tseng, H.-T.; Chatani, Y.; Tadokoro, H. Structural Change of st-PMMA on Drawing, Absorption and Desorption of Solvents Polymer 1982, 23, 1256-1258 10.1016/0032-3861(82)90263-4
    • (1982) Polymer , vol.23 , pp. 1256-1258
    • Kusuyama, H.1    Takase, M.2    Higashiyama, Y.3    Tseng, H.-T.4    Chatani, Y.5    Tadokoro, H.6
  • 125
    • 84958051160 scopus 로고
    • The Effect of Crosslinking on the Aggregation of Syndiotactic Poly(methyl methacrylate)-An Investigation Using NMR and Infrared Spectroscopy
    • Spevacek, J.; Schneider, B.; Stokr, J.; Vlcek, P. The Effect of Crosslinking on the Aggregation of Syndiotactic Poly(methyl methacrylate)-An Investigation Using NMR and Infrared Spectroscopy Makromol. Chem. 1988, 189, 951-959 10.1002/macp.1988.021890425
    • (1988) Makromol. Chem. , vol.189 , pp. 951-959
    • Spevacek, J.1    Schneider, B.2    Stokr, J.3    Vlcek, P.4
  • 126
    • 40949153409 scopus 로고    scopus 로고
    • Encapsulation of Fullerenes in a Helical PMMA Cavity Leading to a Robust Processable Complex with a Macromolecular Helicity Memory
    • Kawauchi, T.; Kumaki, J.; Kitaura, A.; Okoshi, K.; Kusanagi, H.; Kobayashi, K.; Sugai, T.; Shinohara, H.; Yashima, E. Encapsulation of Fullerenes in a Helical PMMA Cavity Leading to a Robust Processable Complex with a Macromolecular Helicity Memory Angew. Chem., Int. Ed. 2008, 47, 515-519 10.1002/anie.200703655
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 515-519
    • Kawauchi, T.1    Kumaki, J.2    Kitaura, A.3    Okoshi, K.4    Kusanagi, H.5    Kobayashi, K.6    Sugai, T.7    Shinohara, H.8    Yashima, E.9
  • 128
    • 0038796507 scopus 로고    scopus 로고
    • Free-Radical Polymerization of (R)-(-)-1-(1-Naphthyl)ethyl(2-methacryloyloxyethyl)urea and Chiral Recognition Ability
    • Lee, Y. K.; Nakashima, Y.; Onimura, K.; Tsutsumi, H.; Oishi, T. Free-Radical Polymerization of (R)-(-)-1-(1-Naphthyl)ethyl(2-methacryloyloxyethyl)urea and Chiral Recognition Ability Macromolecules 2003, 36, 4735-4742 10.1021/ma0216371
    • (2003) Macromolecules , vol.36 , pp. 4735-4742
    • Lee, Y.K.1    Nakashima, Y.2    Onimura, K.3    Tsutsumi, H.4    Oishi, T.5
  • 129
    • 0036194065 scopus 로고    scopus 로고
    • Synthesis of Novel Chiral Poly(methacrylate)s Having Urea Moieties and (S)-Methylbenzyl or l-Phenylalanine Methyl Ester Groups and Their Chiral Recognition Abilities
    • Lee, Y. K.; Hisamitsu, N.; Onimura, K.; Tsutsumi, H.; Oishi, T. Synthesis of Novel Chiral Poly(methacrylate)s Having Urea Moieties and (S)-Methylbenzyl or l-Phenylalanine Methyl Ester Groups and Their Chiral Recognition Abilities Polym. J. 2002, 34, 9-17 10.1295/polymj.34.9
    • (2002) Polym. J. , vol.34 , pp. 9-17
    • Lee, Y.K.1    Hisamitsu, N.2    Onimura, K.3    Tsutsumi, H.4    Oishi, T.5
  • 130
    • 0001606436 scopus 로고
    • Synthesis of Optically Active Polymethacrylates Bearing Axially Dissymmetric 1,1′-Binaphthalene Skeleton as a Pendant Group and Their Optical Resolution Ability as Chiral Adsorbent for HPLC
    • Tamai, Y.; Qian, P.; Matsunaga, K.; Miyano, S. Synthesis of Optically Active Polymethacrylates Bearing Axially Dissymmetric 1,1′-Binaphthalene Skeleton as a Pendant Group and Their Optical Resolution Ability as Chiral Adsorbent for HPLC Bull. Chem. Soc. Jpn. 1992, 65, 817-823 10.1246/bcsj.65.817
    • (1992) Bull. Chem. Soc. Jpn. , vol.65 , pp. 817-823
    • Tamai, Y.1    Qian, P.2    Matsunaga, K.3    Miyano, S.4
  • 131
    • 0033516031 scopus 로고    scopus 로고
    • Optical Resolution of Some Racemates by HPLC Using Chiral Polymers Having (+)-5-Oxobornyl Moieties
    • Liu, J. H.; Tsai, F. Optical Resolution of Some Racemates by HPLC Using Chiral Polymers Having (+)-5-Oxobornyl Moieties J. Appl. Polym. Sci. 1999, 72, 677-682 10.1002/(SICI)1097-4628(19990502)72:5677::AID-APP83.0.CO;2-A
    • (1999) J. Appl. Polym. Sci. , vol.72 , pp. 677-682
    • Liu, J.H.1    Tsai, F.2
  • 132
    • 72949084638 scopus 로고    scopus 로고
    • Photoinduced Racemization of an Optically Active Helical Polymer Formed by the Asymmetric Polymerization of 2,7-Bis(4-tert-butylphenyl)fluoren-9-yl Acrylate
    • Sakamoto, T.; Fukuda, Y.; Sato, S.-I.; Nakano, T. Photoinduced Racemization of an Optically Active Helical Polymer Formed by the Asymmetric Polymerization of 2,7-Bis(4-tert-butylphenyl)fluoren-9-yl Acrylate Angew. Chem., Int. Ed. 2009, 48, 9308-9311 10.1002/anie.200904259
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 9308-9311
    • Sakamoto, T.1    Fukuda, Y.2    Sato, S.-I.3    Nakano, T.4
  • 133
    • 0006676191 scopus 로고
    • Optical Resolution of Alcohols and Amines on Poly[(S)-(-)-p-(p-tolylsulfinyl)styrene] by Means of HPLC
    • Kunieda, N.; Chakihara, H.; Kinoshita, M. Optical Resolution of Alcohols and Amines on Poly[(S)-(-)-p-(p-tolylsulfinyl)styrene] by Means of HPLC Chem. Lett. 1990, 317-318 10.1246/cl.1990.317
    • (1990) Chem. Lett. , pp. 317-318
    • Kunieda, N.1    Chakihara, H.2    Kinoshita, M.3
  • 134
    • 0035033575 scopus 로고    scopus 로고
    • Synthesis and Chiroptical Properties of (S)-(-)-N-α-Methylbenzylmaleimide Polymers Containing Crystallinity
    • Zhou, H.; Onimura, K.; Tsutsumi, H.; Oishi, T. Synthesis and Chiroptical Properties of (S)-(-)-N-α-Methylbenzylmaleimide Polymers Containing Crystallinity Polym. J. 2001, 33, 227-235 10.1295/polymj.33.227
    • (2001) Polym. J. , vol.33 , pp. 227-235
    • Zhou, H.1    Onimura, K.2    Tsutsumi, H.3    Oishi, T.4
  • 135
    • 4544346888 scopus 로고    scopus 로고
    • Asymmetric Anionic Polymerization of Optically Active N-1-Cyclohexylethylmaleimide
    • Onimura, K.; Zhang, Y.; Yagyu, M.; Oishi, T. Asymmetric Anionic Polymerization of Optically Active N-1-Cyclohexylethylmaleimide J. Polym. Sci., Part A: Polym. Chem. 2004, 42, 4682-4692 10.1002/pola.20358
    • (2004) J. Polym. Sci., Part A: Polym. Chem. , vol.42 , pp. 4682-4692
    • Onimura, K.1    Zhang, Y.2    Yagyu, M.3    Oishi, T.4
  • 136
    • 24344474491 scopus 로고    scopus 로고
    • Asymmetric Anionic Polymerizations of (R)-N-Maleoyl-D-phenylglycine Alkyl Esters and Optical Resolution Using Their Polymers
    • Oishi, T.; Zhang, Y.; Fukushima, T.; Onimura, K. Asymmetric Anionic Polymerizations of (R)-N-Maleoyl-D-phenylglycine Alkyl Esters and Optical Resolution Using Their Polymers Polym. J. 2005, 37, 453-463 10.1295/polymj.37.453
    • (2005) Polym. J. , vol.37 , pp. 453-463
    • Oishi, T.1    Zhang, Y.2    Fukushima, T.3    Onimura, K.4
  • 137
    • 34948873082 scopus 로고    scopus 로고
    • Asymmetric Polymerizations of (S)-N-Maleoyl-L-leucine Alkyl Ester and Chiral Recognition Ability of its Polymer as Chiral Stationary Phase for HPLC
    • Gao, H. J.; Isobe, Y.; Onimura, K.; Oishi, T. Asymmetric Polymerizations of (S)-N-Maleoyl-L-leucine Alkyl Ester and Chiral Recognition Ability of its Polymer as Chiral Stationary Phase for HPLC Polym. J. 2007, 39, 764-776 10.1295/polymj.PJ2006231
    • (2007) Polym. J. , vol.39 , pp. 764-776
    • Gao, H.J.1    Isobe, Y.2    Onimura, K.3    Oishi, T.4
  • 138
    • 36949016041 scopus 로고    scopus 로고
    • Asymmetric Polymerizations of N-Substituted Meleimides Bearing L-leucine Esters Derivatives and Chiral Recognition Abilities of Their Polymers
    • Oishi, T.; Gao, H. J.; Nakamura, T.; Isobe, Y.; Onimura, K. Asymmetric Polymerizations of N-Substituted Meleimides Bearing L-leucine Esters Derivatives and Chiral Recognition Abilities of Their Polymers Polym. J. 2007, 39, 1047-1059 10.1295/polymj.PJ2007022
    • (2007) Polym. J. , vol.39 , pp. 1047-1059
    • Oishi, T.1    Gao, H.J.2    Nakamura, T.3    Isobe, Y.4    Onimura, K.5
  • 139
    • 0033616111 scopus 로고    scopus 로고
    • Well-Controlled Polymerization of Phenylacetylenes with Organorhodium(I) Complexes: Mechanism and Structure of the Polyenes
    • Kishimoto, Y.; Eckerle, P.; Miyatake, T.; Kainosho, M.; Ono, A.; Ikariya, T.; Noyori, R. Well-Controlled Polymerization of Phenylacetylenes with Organorhodium(I) Complexes: Mechanism and Structure of the Polyenes J. Am. Chem. Soc. 1999, 121, 12035-12044 10.1021/ja991903z
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 12035-12044
    • Kishimoto, Y.1    Eckerle, P.2    Miyatake, T.3    Kainosho, M.4    Ono, A.5    Ikariya, T.6    Noyori, R.7
  • 140
    • 0001415562 scopus 로고    scopus 로고
    • Enantioseparation on Optically Active Stereoregular Polyphenylacetylene Derivatives as Chiral Stationary Phases for HPLC
    • Yashima, E.; Matsushima, T.; Nimura, T.; Okamoto, Y. Enantioseparation on Optically Active Stereoregular Polyphenylacetylene Derivatives as Chiral Stationary Phases for HPLC Korea Polym. J. 1996, 4, 139-146
    • (1996) Korea Polym. J. , vol.4 , pp. 139-146
    • Yashima, E.1    Matsushima, T.2    Nimura, T.3    Okamoto, Y.4
  • 141
    • 38149070118 scopus 로고    scopus 로고
    • Synthesis of Hydroxy Group-Containing Poly(N-propargylamides): Examination of the Secondary Structure and Chiral-Recognition Ability of the Polymers
    • Sanda, F.; Fujii, T.; Tabei, J.; Shiotsuki, M.; Masuda, T. Synthesis of Hydroxy Group-Containing Poly(N-propargylamides): Examination of the Secondary Structure and Chiral-Recognition Ability of the Polymers Macromol. Chem. Phys. 2008, 209, 112-118 10.1002/macp.200700374
    • (2008) Macromol. Chem. Phys. , vol.209 , pp. 112-118
    • Sanda, F.1    Fujii, T.2    Tabei, J.3    Shiotsuki, M.4    Masuda, T.5
  • 142
    • 28144443427 scopus 로고    scopus 로고
    • New Macromolecular Architectures for Permselective Membranes-Gas Permselective Membranes from Dendrimers and Enantioselectively Permeable Membranes from One-handed Helical Polymers
    • Aoki, T.; Kaneko, T. New Macromolecular Architectures for Permselective Membranes-Gas Permselective Membranes from Dendrimers and Enantioselectively Permeable Membranes from One-handed Helical Polymers Polym. J. 2005, 37, 717-735 10.1295/polymj.37.717
    • (2005) Polym. J. , vol.37 , pp. 717-735
    • Aoki, T.1    Kaneko, T.2
  • 143
    • 4544277915 scopus 로고    scopus 로고
    • Synthesis of Chiral Helical Poly[p-(oligopinanylsiloxanyl)phenylacetylene]s and Enantioselective Permeability of Their Membranes
    • Aoki, T.; Fukuda, T.; Shinohara, K. I.; Kaneko, T.; Teraguchi, M.; Yagi, M. Synthesis of Chiral Helical Poly[p-(oligopinanylsiloxanyl)phenylacetylene]s and Enantioselective Permeability of Their Membranes J. Polym. Sci., Part A: Polym. Chem. 2004, 42, 4502-4517 10.1002/pola.20356
    • (2004) J. Polym. Sci., Part A: Polym. Chem. , vol.42 , pp. 4502-4517
    • Aoki, T.1    Fukuda, T.2    Shinohara, K.I.3    Kaneko, T.4    Teraguchi, M.5    Yagi, M.6
  • 144
    • 84893510282 scopus 로고    scopus 로고
    • Synthesis and Enantioselective Permeability of One-handed Helical Multihydroxy Poly(phenylacetylene) Membrane by in Situ Removal of the Original Chiral Substituents
    • Liu, L.; Mottate, K.; Aoki, T.; Kaneko, T.; Teraguchi, M. Synthesis and Enantioselective Permeability of One-handed Helical Multihydroxy Poly(phenylacetylene) Membrane by In Situ Removal of the Original Chiral Substituents Chem. Lett. 2014, 43, 237-239 10.1246/cl.130896
    • (2014) Chem. Lett. , vol.43 , pp. 237-239
    • Liu, L.1    Mottate, K.2    Aoki, T.3    Kaneko, T.4    Teraguchi, M.5
  • 145
    • 84875995273 scopus 로고    scopus 로고
    • Influence of Stereoregularity and Linkage Groups on Chiral Recognition of Poly(phenylacetylene) Derivatives Bearing L-Leucine Ethyl Ester Pendants as Chiral Stationary Phases for HPLC
    • Zhang, C.; Liu, F.; Li, Y.; Shen, X.; Xu, X.; Sakai, R.; Satoh, T.; Kakuchi, T.; Okamoto, Y. Influence of Stereoregularity and Linkage Groups on Chiral Recognition of Poly(phenylacetylene) Derivatives Bearing L-Leucine Ethyl Ester Pendants as Chiral Stationary Phases for HPLC J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 2271-2278 10.1002/pola.26611
    • (2013) J. Polym. Sci., Part A: Polym. Chem. , vol.51 , pp. 2271-2278
    • Zhang, C.1    Liu, F.2    Li, Y.3    Shen, X.4    Xu, X.5    Sakai, R.6    Satoh, T.7    Kakuchi, T.8    Okamoto, Y.9
  • 146
    • 84887600521 scopus 로고    scopus 로고
    • Synthesis of Helical Poly(Phenylacetylene)s with Amide Linkage Bearing L-Phenylalanine and L-Phenylglycine Ethyl Ester Pendants and Their Applications as Chiral Stationary Phases for HPLC
    • Zhang, C.; Wang, H.; Geng, Q.; Yang, T.; Liu, L.; Sakai, R.; Satoh, T.; Kakuchi, T.; Okamoto, Y. Synthesis of Helical Poly(Phenylacetylene)s with Amide Linkage Bearing L-Phenylalanine and L-Phenylglycine Ethyl Ester Pendants and Their Applications as Chiral Stationary Phases for HPLC Macromolecules 2013, 46, 8406-8415 10.1021/ma4015802
    • (2013) Macromolecules , vol.46 , pp. 8406-8415
    • Zhang, C.1    Wang, H.2    Geng, Q.3    Yang, T.4    Liu, L.5    Sakai, R.6    Satoh, T.7    Kakuchi, T.8    Okamoto, Y.9
  • 147
    • 45449094436 scopus 로고    scopus 로고
    • Synthesis and Chiral Recognition Properties of Poly(N-propargylamide) Gels Derived from Ornithine and Lysine
    • Liu, R. Y.; Sanda, F.; Masuda, T. Synthesis and Chiral Recognition Properties of Poly(N-propargylamide) Gels Derived from Ornithine and Lysine J. Polym. Sci., Part A: Polym. Chem. 2008, 46, 4175-4182 10.1002/pola.22766
    • (2008) J. Polym. Sci., Part A: Polym. Chem. , vol.46 , pp. 4175-4182
    • Liu, R.Y.1    Sanda, F.2    Masuda, T.3
  • 148
    • 84864427113 scopus 로고    scopus 로고
    • Enantioseparation on Helical Poly(phenylacetylene)s Bearing Cinchona Alkaloid Pendants as Chiral Stationary Phases for HPLC
    • Naito, Y.; Tang, Z.; Iida, H.; Miyabe, T.; Yashima, E. Enantioseparation on Helical Poly(phenylacetylene)s Bearing Cinchona Alkaloid Pendants as Chiral Stationary Phases for HPLC Chem. Lett. 2012, 41, 809-811 10.1246/cl.2012.809
    • (2012) Chem. Lett. , vol.41 , pp. 809-811
    • Naito, Y.1    Tang, Z.2    Iida, H.3    Miyabe, T.4    Yashima, E.5
  • 150
    • 84899099313 scopus 로고    scopus 로고
    • Switchable Enantioseparation Based on Macromolecular Memory of a Helical Polyacetylene in the Solid State
    • Shimomura, K.; Ikai, T.; Kanoh, S.; Yashima, E.; Maeda, K. Switchable Enantioseparation Based on Macromolecular Memory of a Helical Polyacetylene in the Solid State Nat. Chem. 2014, 6, 429-434 10.1038/nchem.1916
    • (2014) Nat. Chem. , vol.6 , pp. 429-434
    • Shimomura, K.1    Ikai, T.2    Kanoh, S.3    Yashima, E.4    Maeda, K.5
  • 151
    • 84882733159 scopus 로고    scopus 로고
    • Au@Poly(N-propargylamide) Nanoparticles: Preparation and Chiral Recognition
    • Zhang, C.; Song, C.; Yang, W.; Deng, J. Au@Poly(N-propargylamide) Nanoparticles: Preparation and Chiral Recognition Macromol. Rapid Commun. 2013, 34, 1319-1324 10.1002/marc.201300355
    • (2013) Macromol. Rapid Commun. , vol.34 , pp. 1319-1324
    • Zhang, C.1    Song, C.2    Yang, W.3    Deng, J.4
  • 152
    • 0346665529 scopus 로고    scopus 로고
    • Resolution of Enantiomers Using Sugar-Carrying Polyisocyanides as Chiral Stationary Phases for HPLC
    • Tsuchida, A.; Hasegawa, T.; Kobayashi, K.; Yamamoto, C.; Okamoto, Y. Resolution of Enantiomers Using Sugar-Carrying Polyisocyanides as Chiral Stationary Phases for HPLC Bull. Chem. Soc. Jpn. 2002, 75, 2681-2685 10.1246/bcsj.75.2681
    • (2002) Bull. Chem. Soc. Jpn. , vol.75 , pp. 2681-2685
    • Tsuchida, A.1    Hasegawa, T.2    Kobayashi, K.3    Yamamoto, C.4    Okamoto, Y.5
  • 153
    • 33748223118 scopus 로고
    • Reaction of Heterodinuclear μ-Ethynediyl Complexes Containing Palladium and Platinum: Multiple and Successive Insertion of Isocyanides
    • Onitsuka, K.; Joh, T.; Takahashi, S. Reaction of Heterodinuclear μ-Ethynediyl Complexes Containing Palladium and Platinum: Multiple and Successive Insertion of Isocyanides Angew. Chem., Int. Ed. Engl. 1992, 31, 851-852 10.1002/anie.199208511
    • (1992) Angew. Chem., Int. Ed. Engl. , vol.31 , pp. 851-852
    • Onitsuka, K.1    Joh, T.2    Takahashi, S.3
  • 154
    • 0035813936 scopus 로고    scopus 로고
    • Helical Chiral Polyisocyanides Possessing Porphyrin Pendants: Determination of Helicity by Exciton-Coupled Circular Dichroism
    • Takei, F.; Hayashi, H.; Onitsuka, K.; Kobayashi, N.; Takahashi, S. Helical Chiral Polyisocyanides Possessing Porphyrin Pendants: Determination of Helicity by Exciton-Coupled Circular Dichroism Angew. Chem., Int. Ed. 2001, 40, 4092-4094 10.1002/1521-3773(20011105)40:214092::AID-ANIE40923.0.CO;2-R
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4092-4094
    • Takei, F.1    Hayashi, H.2    Onitsuka, K.3    Kobayashi, N.4    Takahashi, S.5
  • 156
    • 67650519810 scopus 로고    scopus 로고
    • Enantiomer-selective and Helix-sense-selective Living Block Copolymerization of Isocyanide Enantiomers Initiated by Single-handed Helical Poly(phenyl isocyanide)s
    • Wu, Z.-Q.; Nagai, K.; Banno, M.; Okoshi, K.; Onitsuka, K.; Yashima, E. Enantiomer-selective and Helix-sense-selective Living Block Copolymerization of Isocyanide Enantiomers Initiated by Single-handed Helical Poly(phenyl isocyanide)s J. Am. Chem. Soc. 2009, 131, 6708-6718 10.1021/ja900036n
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 6708-6718
    • Wu, Z.-Q.1    Nagai, K.2    Banno, M.3    Okoshi, K.4    Onitsuka, K.5    Yashima, E.6
  • 157
    • 78650117165 scopus 로고    scopus 로고
    • Separation of Enantiomers on Diastereomeric Right- and Left-handed Helical Poly(phenyl isocyanide)s Bearing L-Alanine Pendants Immobilized on Silica Gel by HPLC
    • Tamura, K.; Miyabe, T.; Iida, H.; Yashima, E. Separation of Enantiomers on Diastereomeric Right- and Left-handed Helical Poly(phenyl isocyanide)s Bearing L-Alanine Pendants Immobilized on Silica Gel by HPLC Polym. Chem. 2011, 2, 91-98 10.1039/C0PY00164C
    • (2011) Polym. Chem. , vol.2 , pp. 91-98
    • Tamura, K.1    Miyabe, T.2    Iida, H.3    Yashima, E.4
  • 158
    • 84857264919 scopus 로고    scopus 로고
    • Enantioseparation on Poly(phenyl isocyanide)s with Macromolecular Helicity Memory as Chiral Stationary Phases for HPLC
    • Miyabe, T.; Iida, H.; Yashima, E. Enantioseparation on Poly(phenyl isocyanide)s with Macromolecular Helicity Memory as Chiral Stationary Phases for HPLC Chem. Sci. 2012, 3, 863-867 10.1039/C1SC00708D
    • (2012) Chem. Sci. , vol.3 , pp. 863-867
    • Miyabe, T.1    Iida, H.2    Yashima, E.3
  • 159
    • 0033519678 scopus 로고    scopus 로고
    • Memory of Macromolecular Helicity Assisted by Interaction with Achiral Small Molecules
    • Yashima, E.; Maeda, K.; Okamoto, Y. Memory of Macromolecular Helicity Assisted by Interaction with Achiral Small Molecules Nature 1999, 399, 449-451 10.1038/20900
    • (1999) Nature , vol.399 , pp. 449-451
    • Yashima, E.1    Maeda, K.2    Okamoto, Y.3
  • 160
    • 1642494633 scopus 로고    scopus 로고
    • An Unprecedented Memory of Macromolecular Helicity Induced in an Achiral Polyisocyanide in Water
    • Ishikawa, M.; Maeda, K.; Mitsutsuji, Y.; Yashima, E. An Unprecedented Memory of Macromolecular Helicity Induced in an Achiral Polyisocyanide in Water J. Am. Chem. Soc. 2004, 126, 732-733 10.1021/ja039279k
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 732-733
    • Ishikawa, M.1    Maeda, K.2    Mitsutsuji, Y.3    Yashima, E.4
  • 161
    • 53449098640 scopus 로고    scopus 로고
    • Single- and Double-stranded helical Polymers: Synthesis, Structures, and Functions
    • Yashima, E.; Maeda, K.; Furusho, Y. Single- and Double-stranded helical Polymers: Synthesis, Structures, and Functions Acc. Chem. Res. 2008, 41, 1166-1180 10.1021/ar800091w
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1166-1180
    • Yashima, E.1    Maeda, K.2    Furusho, Y.3
  • 162
    • 73249140329 scopus 로고    scopus 로고
    • Helical polymers: Synthesis, Structures, and Functions
    • Yashima, E.; Maeda, K.; Iida, H.; Furusho, Y.; Nagai, K. Helical polymers: Synthesis, Structures, and Functions Chem. Rev. 2009, 109, 6102-6211 10.1021/cr900162q
    • (2009) Chem. Rev. , vol.109 , pp. 6102-6211
    • Yashima, E.1    Maeda, K.2    Iida, H.3    Furusho, Y.4    Nagai, K.5
  • 163
    • 84863837244 scopus 로고    scopus 로고
    • Enhanced Catalyst Activity and Enantioselectivity with Chirality-Switchable Polymer Ligand PQXphos in Pd-Catalyzed Asymmetric Silaborative Cleavage of meso-Methylenecyclopropanes
    • Akai, Y.; Yamamoto, T.; Nagata, Y.; Ohmura, T.; Suginome, M. Enhanced Catalyst Activity and Enantioselectivity with Chirality-Switchable Polymer Ligand PQXphos in Pd-Catalyzed Asymmetric Silaborative Cleavage of meso-Methylenecyclopropanes J. Am. Chem. Soc. 2012, 134, 11092-11095 10.1021/ja303506k
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 11092-11095
    • Akai, Y.1    Yamamoto, T.2    Nagata, Y.3    Ohmura, T.4    Suginome, M.5
  • 164
    • 84910011185 scopus 로고    scopus 로고
    • Poly(quinoxaline-2,3-diyl)s Bearing (S)-3-Octyloxymethyl Side Chains as an Efficient Amplifier of Alkane Solvent Effect Leading to Switch of Main-Chain Helical Chirality
    • Nagata, Y.; Nishikawa, T.; Suginome, M. Poly(quinoxaline-2,3-diyl)s Bearing (S)-3-Octyloxymethyl Side Chains as an Efficient Amplifier of Alkane Solvent Effect Leading to Switch of Main-Chain Helical Chirality J. Am. Chem. Soc. 2014, 136, 15901-15904 10.1021/ja509531t
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 15901-15904
    • Nagata, Y.1    Nishikawa, T.2    Suginome, M.3
  • 165
    • 0001404637 scopus 로고
    • Optically Active Polyisocyanates
    • Goodman, M.; Chen, S. Optically Active Polyisocyanates Macromolecules 1970, 3, 398-402 10.1021/ma60016a005
    • (1970) Macromolecules , vol.3 , pp. 398-402
    • Goodman, M.1    Chen, S.2
  • 166
    • 0001557750 scopus 로고
    • Optically Active Polyisocyanates. II
    • Goodman, M.; Chen, S. Optically Active Polyisocyanates. II Macromolecules 1971, 4, 625-629 10.1021/ma60023a023
    • (1971) Macromolecules , vol.4 , pp. 625-629
    • Goodman, M.1    Chen, S.2
  • 167
    • 33845280516 scopus 로고
    • Macromolecular Stereochemistry: A Cooperative Deuterium Isotope Effect Leading to a Large Optical Rotation
    • Green, M. M.; Andreola, C.; Munoz, B.; Reidy, M. Macromolecular Stereochemistry: A Cooperative Deuterium Isotope Effect Leading to a Large Optical Rotation J. Am. Chem. Soc. 1988, 110, 4063-4065 10.1021/ja00220a070
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 4063-4065
    • Green, M.M.1    Andreola, C.2    Munoz, B.3    Reidy, M.4
  • 168
    • 0024843350 scopus 로고
    • Macromolecular Stereochemistry: Helical Sense Preference in Optically Active Polyisocyanates. Amplification of a Conformational Equilibrium Deuterium Isotope Effect
    • Lifson, S.; Andreola, C.; Peterson, N. C.; Green, M. M. Macromolecular Stereochemistry: Helical Sense Preference in Optically Active Polyisocyanates. Amplification of a Conformational Equilibrium Deuterium Isotope Effect J. Am. Chem. Soc. 1989, 111, 8850-8858 10.1021/ja00206a013
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 8850-8858
    • Lifson, S.1    Andreola, C.2    Peterson, N.C.3    Green, M.M.4
  • 169
    • 33845184268 scopus 로고
    • Macromolecular Stereochemistry: the Out-of-proportion Influence of Optically Active Comonomers on the Conformational Characteristics of Polyisocyanates. the Sergeants and Soldiers Experiment
    • Green, M. M.; Reidy, M. P. Macromolecular Stereochemistry: The Out-of-proportion Influence of Optically Active Comonomers on the Conformational Characteristics of Polyisocyanates. The Sergeants and Soldiers Experiment J. Am. Chem. Soc. 1989, 111, 6452-6454 10.1021/ja00198a084
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 6452-6454
    • Green, M.M.1    Reidy, M.P.2
  • 171
    • 0027151618 scopus 로고
    • Asymmetric Polymerization of Isocyanates with Optically Active Anionic Initiators
    • Okamoto, Y.; Matsuda, M.; Nakano, T.; Yashima, E. Asymmetric Polymerization of Isocyanates with Optically Active Anionic Initiators Polym. J. 1993, 25, 391-396 10.1295/polymj.25.391
    • (1993) Polym. J. , vol.25 , pp. 391-396
    • Okamoto, Y.1    Matsuda, M.2    Nakano, T.3    Yashima, E.4
  • 172
    • 0028338196 scopus 로고
    • Asymmetric Polymerization of Aromatic Isocyanates with Optically Active Anionnic Initiators
    • Okamoto, Y.; Matsuda, M.; Nakano, T.; Yashima, E. Asymmetric Polymerization of Aromatic Isocyanates with Optically Active Anionnic Initiators J. Polym. Sci., Part A: Polym. Chem. 1994, 32, 309-315 10.1002/pola.1994.080320212
    • (1994) J. Polym. Sci., Part A: Polym. Chem. , vol.32 , pp. 309-315
    • Okamoto, Y.1    Matsuda, M.2    Nakano, T.3    Yashima, E.4
  • 173
    • 0029207899 scopus 로고
    • Chiroptical Properties of Oligomers of m-Methylphenyl Isocyanate Bearing an Optically Active End-Group
    • Maeda, K.; Matsuda, M.; Nakano, T.; Okamoto, Y. Chiroptical Properties of Oligomers of m-Methylphenyl Isocyanate Bearing an Optically Active End-Group Polym. J. 1995, 27, 141-146 10.1295/polymj.27.141
    • (1995) Polym. J. , vol.27 , pp. 141-146
    • Maeda, K.1    Matsuda, M.2    Nakano, T.3    Okamoto, Y.4
  • 174
    • 0032002936 scopus 로고    scopus 로고
    • Synthesis and Conformation of Optically Active Poly(phenyl isocyanate)s Bearing an ((S)-(α-Methylbenzyl)carbamoyl) Group
    • Maeda, K.; Okamoto, Y. Synthesis and Conformation of Optically Active Poly(phenyl isocyanate)s Bearing an ((S)-(α-Methylbenzyl)carbamoyl) Group Macromolecules 1998, 31, 1046-1052 10.1021/ma970948m
    • (1998) Macromolecules , vol.31 , pp. 1046-1052
    • Maeda, K.1    Okamoto, Y.2
  • 175
    • 30344474600 scopus 로고    scopus 로고
    • Chiral Discrimination of a Helically Organized Crown Ether Array Parallel to the Helix Axis of Polyisocyanate
    • Sakai, R.; Otsuka, I.; Satoh, T.; Kakuchi, R.; Kaga, H.; Kakuchi, T. Chiral Discrimination of a Helically Organized Crown Ether Array Parallel to the Helix Axis of Polyisocyanate J. Polym. Sci., Part A: Polym. Chem. 2006, 44, 325-334 10.1002/pola.21074
    • (2006) J. Polym. Sci., Part A: Polym. Chem. , vol.44 , pp. 325-334
    • Sakai, R.1    Otsuka, I.2    Satoh, T.3    Kakuchi, R.4    Kaga, H.5    Kakuchi, T.6
  • 176
    • 0006746278 scopus 로고
    • 5-benzyl-L-glutamine) Covalently Bound to Polystyrene Resin
    • 5-benzyl-L-glutamine) Covalently Bound to Polystyrene Resin J. Chromatogr. 1987, 396, 395-398 10.1016/S0021-9673(01)94081-6
    • (1987) J. Chromatogr. , vol.396 , pp. 395-398
    • Doi, Y.1    Kiniwa, H.2    Nishikaji, T.3    Ogata, N.4
  • 177
    • 0023749434 scopus 로고
    • Chromatographic Resolution of Dipeptide Enantiomers and Diastereomers on Chiral Stationary Phases from Poly(L-leucine) or Poly(L-phenylalanine)
    • Hirayama, C.; Ihara, H.; Tanaka, K. Chromatographic Resolution of Dipeptide Enantiomers and Diastereomers on Chiral Stationary Phases from Poly(L-leucine) or Poly(L-phenylalanine) J. Chromatogr. A 1988, 450, 271-276 10.1016/S0021-9673(01)83580-9
    • (1988) J. Chromatogr. A , vol.450 , pp. 271-276
    • Hirayama, C.1    Ihara, H.2    Tanaka, K.3
  • 178
    • 14144251632 scopus 로고    scopus 로고
    • Chromatographic Evaluation of Poly(trans-1,2-cyclohexanediyl-bis acrylamide) as a Chiral Stationary Phase for HPLC
    • Zhong, Q.; Han, X.; He, L.; Beesley, T. E.; Trahanovsky, W. S.; Armstrong, D. W. Chromatographic Evaluation of Poly(trans-1,2-cyclohexanediyl-bis acrylamide) as a Chiral Stationary Phase for HPLC J. Chromatogr. A 2005, 1066, 55-70 10.1016/j.chroma.2004.12.088
    • (2005) J. Chromatogr. A , vol.1066 , pp. 55-70
    • Zhong, Q.1    Han, X.2    He, L.3    Beesley, T.E.4    Trahanovsky, W.S.5    Armstrong, D.W.6
  • 179
    • 30344476434 scopus 로고    scopus 로고
    • Synthesis and Evaluation of a Synthetic Polymeric Chiral Stationary Phase for LC Based on the N,N′-[(1R,2R)-1,2-Diphenyl-1,2-ethanediyl]bis-2-propenamide Monomer
    • Han, X.; He, L.; Zhong, Q.; Beesley, T. E.; Armstrong, D. W. Synthesis and Evaluation of a Synthetic Polymeric Chiral Stationary Phase for LC Based on the N,N′-[(1R,2R)-1,2-Diphenyl-1,2-ethanediyl]bis-2-propenamide Monomer Chromatographia 2006, 63, 13-23 10.1365/s10337-005-0696-3
    • (2006) Chromatographia , vol.63 , pp. 13-23
    • Han, X.1    He, L.2    Zhong, Q.3    Beesley, T.E.4    Armstrong, D.W.5
  • 180
    • 33947573338 scopus 로고    scopus 로고
    • Preparation and Evaluation of a New Synthetic Polymeric Chiral Stationary Phase for HPLC Based on the trans-9,10-Dihydro-9,10-ethanoanthracene-(11S,12S)-11,12-dicarboxylic Acid Bis-4-vinylphenylamide Monomer
    • Han, X.; Wang, C.; He, L.; Beesley, T. E.; Armstrong, D. W. Preparation and Evaluation of a New Synthetic Polymeric Chiral Stationary Phase for HPLC Based on the trans-9,10-Dihydro-9,10-ethanoanthracene-(11S,12S)-11,12-dicarboxylic Acid Bis-4-vinylphenylamide Monomer Anal. Bioanal. Chem. 2007, 387, 2681-2697 10.1007/s00216-007-1154-x
    • (2007) Anal. Bioanal. Chem. , vol.387 , pp. 2681-2697
    • Han, X.1    Wang, C.2    He, L.3    Beesley, T.E.4    Armstrong, D.W.5
  • 181
    • 79951813863 scopus 로고    scopus 로고
    • Synthesis and Chromatographic Evaluation of New Polymeric Chiral Stationary Phases Based on Three (1S,2S)-(-)-1,2-Diphenylethylenediamine Derivatives in HPLC and SFC
    • Payagala, T.; Wanigasekara, E.; Armstrong, D. W. Synthesis and Chromatographic Evaluation of New Polymeric Chiral Stationary Phases Based on Three (1S,2S)-(-)-1,2-Diphenylethylenediamine Derivatives in HPLC and SFC Anal. Bioanal. Chem. 2011, 399, 2445-2461 10.1007/s00216-010-4615-6
    • (2011) Anal. Bioanal. Chem. , vol.399 , pp. 2445-2461
    • Payagala, T.1    Wanigasekara, E.2    Armstrong, D.W.3
  • 182
    • 0001514557 scopus 로고
    • New Chiral Stationary Phases for the High-Performance Liquid Chromatographic Resolution of Enantiomers
    • Saigo, K.; Chen, Y.; Kubota, N.; Yashibana, K.; Yonezawa, N.; Hasegawa, M. New Chiral Stationary Phases for the High-Performance Liquid Chromatographic Resolution of Enantiomers Chem. Lett. 1986, 515-518 10.1246/cl.1986.515
    • (1986) Chem. Lett. , pp. 515-518
    • Saigo, K.1    Chen, Y.2    Kubota, N.3    Yashibana, K.4    Yonezawa, N.5    Hasegawa, M.6
  • 183
    • 0026383673 scopus 로고
    • Chromatographic Optical Resolution of Enantiomers on Polyamides Containing 1,2-Disubstituted Cyclohexane Moiety as a Chiral Residue
    • Okamoto, Y.; Nagamura, Y.; Fukumoto, T.; Katada, K. Chromatographic Optical Resolution of Enantiomers on Polyamides Containing 1,2-Disubstituted Cyclohexane Moiety as a Chiral Residue Polym. J. 1991, 23, 1197-1207 10.1295/polymj.23.1197
    • (1991) Polym. J. , vol.23 , pp. 1197-1207
    • Okamoto, Y.1    Nagamura, Y.2    Fukumoto, T.3    Katada, K.4
  • 184
    • 0002770628 scopus 로고
    • Synthesis and Properties of Polyamides Having a Cyclobutanedicarboxylic Acid Derivative as a Component
    • Saigo, K. Synthesis and Properties of Polyamides Having a Cyclobutanedicarboxylic Acid Derivative as a Component Prog. Polym. Sci. 1992, 17, 35-86 10.1016/0079-6700(92)90016-R
    • (1992) Prog. Polym. Sci. , vol.17 , pp. 35-86
    • Saigo, K.1
  • 185
    • 3342884838 scopus 로고
    • Preparation, Chiroptical Properties, and Chiral Recognition Ability of Carbamoylated Polyamides Having (-)-Anti Head-to-Head Coumarin Dimer Component
    • Saigo, K.; Nakamura, M.; Adegawa, Y.; Noguchi, S.; Hasegawa, M. Preparation, Chiroptical Properties, and Chiral Recognition Ability of Carbamoylated Polyamides Having (-)-Anti Head-to-Head Coumarin Dimer Component Chem. Lett. 1989, 337-340 10.1246/cl.1989.337
    • (1989) Chem. Lett. , pp. 337-340
    • Saigo, K.1    Nakamura, M.2    Adegawa, Y.3    Noguchi, S.4    Hasegawa, M.5
  • 186
    • 0025429690 scopus 로고
    • Optically Active Polyamides Consisting of Anti Head-to-Head Coumarin Dimer and α,ω-Alkanediamine. Odd-even Discrimination in Chiral Recognition Ability Depending on the Number of the Diamine Component and Correlation between the Ability and Crystallizability
    • Saigo, K.; Shiwaku, T.; Hayashi, K.; Fujioka, K.; Sukegawa, M.; Chen, Y.; Yonezawa, N.; Hasegawa, M.; Hashimoto, T. Optically Active Polyamides Consisting of Anti Head-to-Head Coumarin Dimer and α,ω-Alkanediamine. Odd-even Discrimination in Chiral Recognition Ability Depending on the Number of the Diamine Component and Correlation between the Ability and Crystallizability Macromolecules 1990, 23, 2830-2836 10.1021/ma00213a002
    • (1990) Macromolecules , vol.23 , pp. 2830-2836
    • Saigo, K.1    Shiwaku, T.2    Hayashi, K.3    Fujioka, K.4    Sukegawa, M.5    Chen, Y.6    Yonezawa, N.7    Hasegawa, M.8    Hashimoto, T.9
  • 187
    • 70349179456 scopus 로고    scopus 로고
    • Doubly Tethered Tertiary Amide Linked and Ionically Bonded Diproline Chiral Stationary Phases
    • Lao, W.; Gan, J. Doubly Tethered Tertiary Amide Linked and Ionically Bonded Diproline Chiral Stationary Phases J. Sep. Sci. 2009, 32, 2359-2368 10.1002/jssc.200900112
    • (2009) J. Sep. Sci. , vol.32 , pp. 2359-2368
    • Lao, W.1    Gan, J.2
  • 188
    • 65649101312 scopus 로고    scopus 로고
    • Evaluation of Triproline and Tri-α-methylproline Chiral Stationary Phases Retention and Enantioseparation Associated with Hydrogen Bonding
    • Lao, W.; Gan, J. Evaluation of Triproline and Tri-α-methylproline Chiral Stationary Phases Retention and Enantioseparation Associated with Hydrogen Bonding J. Chromatogr. A 2009, 1216, 5020-5029 10.1016/j.chroma.2009.04.063
    • (2009) J. Chromatogr. A , vol.1216 , pp. 5020-5029
    • Lao, W.1    Gan, J.2
  • 189
    • 77957020445 scopus 로고    scopus 로고
    • Characterization of Warfarin Unusual Peak Profiles on Oligoproline Chiral High Performance Liquid Chromatography Columns
    • Lao, W.; Gan, J. Characterization of Warfarin Unusual Peak Profiles on Oligoproline Chiral High Performance Liquid Chromatography Columns J. Chromatogr. A 2010, 1217, 6545-6554 10.1016/j.chroma.2010.08.066
    • (2010) J. Chromatogr. A , vol.1217 , pp. 6545-6554
    • Lao, W.1    Gan, J.2
  • 190
    • 0027880680 scopus 로고
    • Chiral Recognition Abilities of New Optically Active Polyurethanes Derived from Chiral 1,3-Diols and Diisocyanates
    • Kobayashi, T.; Kakimoto, M.; Imai, Y. Chiral Recognition Abilities of New Optically Active Polyurethanes Derived from Chiral 1,3-Diols and Diisocyanates Polym. J. 1993, 25, 969-975 10.1295/polymj.25.969
    • (1993) Polym. J. , vol.25 , pp. 969-975
    • Kobayashi, T.1    Kakimoto, M.2    Imai, Y.3
  • 191
    • 0026959729 scopus 로고
    • Optically-active Polyurethanes Containing Coumarin Dimer Component: Synthesis, Characterization, and Chiral Recognition Ability
    • Chen, Y.; Lin, J.-J. Optically-active Polyurethanes Containing Coumarin Dimer Component: Synthesis, Characterization, and Chiral Recognition Ability J. Polym. Sci., Part A: Polym. Chem. 1992, 30, 2699-2707 10.1002/pola.1992.080301305
    • (1992) J. Polym. Sci., Part A: Polym. Chem. , vol.30 , pp. 2699-2707
    • Chen, Y.1    Lin, J.-J.2
  • 192
    • 0028331505 scopus 로고
    • Resolution by High-performance Liquid Chromatography Using Polysaccharide Carbamates and Benzoates as Chiral Stationary Phases
    • Okamoto, Y.; Kaida, Y. Resolution by High-performance Liquid Chromatography Using Polysaccharide Carbamates and Benzoates as Chiral Stationary Phases J. Chromatogr. A 1994, 666, 403-419 10.1016/0021-9673(94)80400-1
    • (1994) J. Chromatogr. A , vol.666 , pp. 403-419
    • Okamoto, Y.1    Kaida, Y.2
  • 193
    • 26844485913 scopus 로고    scopus 로고
    • Polysaccharide-Based Chiral LC Columns
    • Yashima, E.; Yamamoto, C.; Okamoto, Y. Polysaccharide-Based Chiral LC Columns Synlett 1998, 1998, 344-360 10.1055/s-1998-1675
    • (1998) Synlett , vol.1998 , pp. 344-360
    • Yashima, E.1    Yamamoto, C.2    Okamoto, Y.3
  • 194
    • 0032482102 scopus 로고    scopus 로고
    • Derivatives for Chromatographic Separation of Enantiomers
    • Okamoto, Y.; Yashima, E. Derivatives for Chromatographic Separation of Enantiomers Angew. Chem., Int. Ed. 1998, 37, 1020-1043 10.1002/(SICI)1521-3773(19980504)37:81020::AID-ANIE10203.0.CO;2-5
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 1020-1043
    • Okamoto, Y.1    Yashima, E.2
  • 195
    • 0029619335 scopus 로고
    • Chiral Discrimination on Polysaccharides Derivatives
    • Yashima, E.; Okamoto, Y. Chiral Discrimination on Polysaccharides Derivatives Bull. Chem. Soc. Jpn. 1995, 68, 3289-3307 10.1246/bcsj.68.3289
    • (1995) Bull. Chem. Soc. Jpn. , vol.68 , pp. 3289-3307
    • Yashima, E.1    Okamoto, Y.2
  • 196
    • 84902425953 scopus 로고    scopus 로고
    • Carreira, E. M. Yamamoto, H. Elsevier: Amsterdam, Chapter 24
    • Shen, J.; Okamoto, Y. In Comprehensive Chirality; Carreira, E. M.; Yamamoto, H., Eds.; Elsevier: Amsterdam, 2012; Vol. 8, Chapter 24, pp 200-226.
    • (2012) Comprehensive Chirality , vol.8 , pp. 200-226
    • Shen, J.1    Okamoto, Y.2
  • 197
    • 0035847188 scopus 로고    scopus 로고
    • Reversed-Phase Liquid Chromatographic Separation of Enantiomers on Polysaccharide Type Chiral Stationary Phases
    • Tachibana, K.; Ohnishi, A. Reversed-Phase Liquid Chromatographic Separation of Enantiomers on Polysaccharide Type Chiral Stationary Phases J. Chromatogr. A 2001, 906, 127-154 10.1016/S0021-9673(00)00955-9
    • (2001) J. Chromatogr. A , vol.906 , pp. 127-154
    • Tachibana, K.1    Ohnishi, A.2
  • 198
    • 33644812832 scopus 로고    scopus 로고
    • The Use of Polysaccharide Phases in the Separation of Enantiomers
    • Stringham, R. W. The Use of Polysaccharide Phases in the Separation of Enantiomers Adv. Chromatogr. 2006, 44, 257-290 10.1201/9781420027150.ch6
    • (2006) Adv. Chromatogr. , vol.44 , pp. 257-290
    • Stringham, R.W.1
  • 199
    • 0035847277 scopus 로고    scopus 로고
    • Polysaccharide-Based Chiral Stationary Phases for High-Performance Liquid Chromatographic Enantioseparation
    • Yashima, E. Polysaccharide-Based Chiral Stationary Phases for High-Performance Liquid Chromatographic Enantioseparation J. Chromatogr. A 2001, 906, 105-125 10.1016/S0021-9673(00)00501-X
    • (2001) J. Chromatogr. A , vol.906 , pp. 105-125
    • Yashima, E.1
  • 200
    • 84870321171 scopus 로고    scopus 로고
    • Complementary Enantiorecognition Patterns and Specific Method Optimization Aspects on Immobilized Polysaccharide-Derived Chiral Stationary Phases
    • Zhang, T.; Franco, P.; Nguyen, D.; Hamasaki, R.; Miyamoto, S.; Ohnishi, A.; Murakami, T. Complementary Enantiorecognition Patterns and Specific Method Optimization Aspects on Immobilized Polysaccharide-Derived Chiral Stationary Phases J. Chromatogr. A 2012, 1269, 178-188 10.1016/j.chroma.2012.09.071
    • (2012) J. Chromatogr. A , vol.1269 , pp. 178-188
    • Zhang, T.1    Franco, P.2    Nguyen, D.3    Hamasaki, R.4    Miyamoto, S.5    Ohnishi, A.6    Murakami, T.7
  • 201
    • 84985206425 scopus 로고
    • Die Chromatographische Racemattrennung
    • Hesse, G.; Hagel, R. Die Chromatographische Racemattrennung Liebigs Ann. Chem. 1976, 1976, 996-1008 10.1002/jlac.197619760604
    • (1976) Liebigs Ann. Chem. , vol.1976 , pp. 996-1008
    • Hesse, G.1    Hagel, R.2
  • 202
    • 0002139398 scopus 로고
    • Chromatographic Resolution of Racemates on Chiral Stationary Phases. I. Influence of the Supramolecular Structure of Cellulose Triacetate
    • Francotte, E.; Wolf, R. M.; Lohmann, D.; Müller, R. Chromatographic Resolution of Racemates on Chiral Stationary Phases. I. Influence of the Supramolecular Structure of Cellulose Triacetate J. Chromatogr. A 1985, 347, 25-37 10.1016/S0021-9673(01)95466-4
    • (1985) J. Chromatogr. A , vol.347 , pp. 25-37
    • Francotte, E.1    Wolf, R.M.2    Lohmann, D.3    Müller, R.4
  • 203
    • 84963176497 scopus 로고
    • Chromatographic Optical Resolution on Polysaccharides and Their Derivatives
    • Shibata, T.; Okamoto, I.; Ishii, K. Chromatographic Optical Resolution on Polysaccharides and Their Derivatives J. Liq. Chromatogr. 1986, 9, 313-340 10.1080/01483918608076640
    • (1986) J. Liq. Chromatogr. , vol.9 , pp. 313-340
    • Shibata, T.1    Okamoto, I.2    Ishii, K.3
  • 204
    • 0006598577 scopus 로고
    • Chromatographic Chiral Resolution. XIV. Cellulose Tribenzoate Derivatives as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Okamoto, Y.; Aburatani, R.; Hatada, K. Chromatographic Chiral Resolution. XIV. Cellulose Tribenzoate Derivatives as Chiral Stationary Phases for High-Performance Liquid Chromatography J. Chromatogr. A 1987, 389, 95-102 10.1016/S0021-9673(01)94414-0
    • (1987) J. Chromatogr. A , vol.389 , pp. 95-102
    • Okamoto, Y.1    Aburatani, R.2    Hatada, K.3
  • 205
    • 74049143458 scopus 로고    scopus 로고
    • Enantioseparation Using Amylose Esters as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Sugiura, Y.; Yamamoto, C.; Okamoto, Y. Enantioseparation Using Amylose Esters as Chiral Stationary Phases for High-Performance Liquid Chromatography Polym. J. 2010, 42, 31-36 10.1038/pj.2009.300
    • (2010) Polym. J. , vol.42 , pp. 31-36
    • Sugiura, Y.1    Yamamoto, C.2    Okamoto, Y.3
  • 206
    • 43949088504 scopus 로고    scopus 로고
    • Synthesis, Resolution, and VCD Analysis of an Enantiopure Diazaoxatricornan Derivative
    • Mobian, P.; Nicolas, C.; Francotte, E.; Bürgi, T.; Lacour, J. Synthesis, Resolution, and VCD Analysis of an Enantiopure Diazaoxatricornan Derivative J. Am. Chem. Soc. 2008, 130, 6507-6514 10.1021/ja800262j
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 6507-6514
    • Mobian, P.1    Nicolas, C.2    Francotte, E.3    Bürgi, T.4    Lacour, J.5
  • 207
    • 41849133225 scopus 로고    scopus 로고
    • Arylbiphenylene Atropisomers: Structure, Conformation, Stereodynamics, and Absolute Configuration
    • Lunazzi, L.; Mancinelli, M.; Mazzanti, A. Arylbiphenylene Atropisomers: Structure, Conformation, Stereodynamics, and Absolute Configuration J. Org. Chem. 2008, 73, 2198-2205 10.1021/jo702502n
    • (2008) J. Org. Chem. , vol.73 , pp. 2198-2205
    • Lunazzi, L.1    Mancinelli, M.2    Mazzanti, A.3
  • 208
    • 0029080398 scopus 로고
    • Enantioselective Total Synthesis of Gracilins B and C Using Catalytic Asymmetric Diels-Alder Methodology
    • Corey, E. J.; Letavic, M. A. Enantioselective Total Synthesis of Gracilins B and C Using Catalytic Asymmetric Diels-Alder Methodology J. Am. Chem. Soc. 1995, 117, 9616-9617 10.1021/ja00142a051
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 9616-9617
    • Corey, E.J.1    Letavic, M.A.2
  • 209
    • 0030444308 scopus 로고    scopus 로고
    • First Catalytic Enantioselective Proton Abstraction Using Chiral Alkoxides
    • Amadji, M.; Vadecard, J.; Plaquevent, J.-C.; Duhamel, L.; Duhaniel, P. First Catalytic Enantioselective Proton Abstraction Using Chiral Alkoxides J. Am. Chem. Soc. 1996, 118, 12483-12484 10.1021/ja960816t
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 12483-12484
    • Amadji, M.1    Vadecard, J.2    Plaquevent, J.-C.3    Duhamel, L.4    Duhaniel, P.5
  • 211
    • 0031046480 scopus 로고    scopus 로고
    • A Novel Axially Dissymmetric Chiral Ligand Based on Amine N-Oxide: (R)- and (S)-3,3′-Dimethyl-2,2′-biquinoline N,N′-dioxide
    • Nakajima, M.; Sasaki, Y.; Shiro, M.; Hashimoto, S. A Novel Axially Dissymmetric Chiral Ligand Based on Amine N-Oxide: (R)- and (S)-3,3′-Dimethyl-2,2′-biquinoline N,N′-dioxide Tetrahedron: Asymmetry 1997, 8, 341-344 10.1016/S0957-4166(96)00521-6
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 341-344
    • Nakajima, M.1    Sasaki, Y.2    Shiro, M.3    Hashimoto, S.4
  • 212
    • 0029161639 scopus 로고
    • Synthesis of Optically Active Aporphine and Morphinandienone Alkaloids via p-Quinol Esters
    • Hara, H.; Komoriya, S.; Miyashita, T.; Hoshino, O. Synthesis of Optically Active Aporphine and Morphinandienone Alkaloids via p-Quinol Esters Tetrahedron: Asymmetry 1995, 6, 1683-1692 10.1016/0957-4166(95)00213-9
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 1683-1692
    • Hara, H.1    Komoriya, S.2    Miyashita, T.3    Hoshino, O.4
  • 213
    • 0028060419 scopus 로고
    • Enantioselective Protonation of Samarium Enolates by a C2-Symmetric Chiral Diol
    • Takeuchi, S.; Ohira, A.; Miyoshi, N.; Mashio, H.; Ohga, Y. Enantioselective Protonation of Samarium Enolates by a C2-Symmetric Chiral Diol Tetrahedron: Asymmetry 1994, 5, 1763-1780 10.1016/0957-4166(94)80086-3
    • (1994) Tetrahedron: Asymmetry , vol.5 , pp. 1763-1780
    • Takeuchi, S.1    Ohira, A.2    Miyoshi, N.3    Mashio, H.4    Ohga, Y.5
  • 214
    • 0026572213 scopus 로고
    • Modulation of the Chiral Recognition by Varation of the Position of the Methyl Group on the Aromatic Ring
    • Francotte, E.; Wolf, R. M. Modulation of the Chiral Recognition by Varation of the Position of the Methyl Group on the Aromatic Ring J. Chromatogr. 1992, 595, 63-75 10.1016/0021-9673(92)85147-L
    • (1992) J. Chromatogr. , vol.595 , pp. 63-75
    • Francotte, E.1    Wolf, R.M.2
  • 215
    • 0029565116 scopus 로고
    • Supramolecular Effects in the Chiral Discrimination of meta-Methylbenzoyl Cellulose in High-Performance Liquid Chromatography
    • Francotte, E.; Zhang, T. Supramolecular Effects in the Chiral Discrimination of meta-Methylbenzoyl Cellulose in High-Performance Liquid Chromatography J. Chromatogr. A 1995, 718, 257-266 10.1016/0021-9673(95)00686-9
    • (1995) J. Chromatogr. A , vol.718 , pp. 257-266
    • Francotte, E.1    Zhang, T.2
  • 216
    • 33748560075 scopus 로고    scopus 로고
    • Preparation of HPLC Chiral Packing Materials Using Cellulose Tris(4-methylbenzoate) for the Separation of Chrysanthemate Isomers
    • Yamamoto, C.; Yamada, K.; Motoya, K.; Kamiya, Y.; Kamigaito, M.; Okamoto, Y.; Aratani, T. Preparation of HPLC Chiral Packing Materials Using Cellulose Tris(4-methylbenzoate) for the Separation of Chrysanthemate Isomers J. Polym. Sci., Part A: Polym. Chem. 2006, 44, 5087-5097 10.1002/pola.21620
    • (2006) J. Polym. Sci., Part A: Polym. Chem. , vol.44 , pp. 5087-5097
    • Yamamoto, C.1    Yamada, K.2    Motoya, K.3    Kamiya, Y.4    Kamigaito, M.5    Okamoto, Y.6    Aratani, T.7
  • 217
    • 0035820003 scopus 로고    scopus 로고
    • Synthesis of An Amylose-Polymer Inclusion Complex by Enzymatic Polymerization of Glucose 1-Phosphate Catalyzed by Phosphorylase Enzyme in the Presence of PolyTHF: A New Method for Synthesis of Polymer-Polymer Inclusion Complexes
    • Kadokawa, J.; Kaneko, Y.; Tagaya, H.; Chiba, K. Synthesis of An Amylose-Polymer Inclusion Complex by Enzymatic Polymerization of Glucose 1-Phosphate Catalyzed by Phosphorylase Enzyme in the Presence of PolyTHF: A New Method for Synthesis of Polymer-Polymer Inclusion Complexes Chem. Commun. 2001, 449-450 10.1039/b008180i
    • (2001) Chem. Commun. , pp. 449-450
    • Kadokawa, J.1    Kaneko, Y.2    Tagaya, H.3    Chiba, K.4
  • 220
  • 221
    • 79960428475 scopus 로고    scopus 로고
    • Synthesis and Chiral Recognition Ability of a Poly(phenylenevinylene)-Encapsulated Amylose Derivative
    • Tamura, K.; Sam, N. S. M.; Ikai, T.; Okamoto, Y.; Yashima, E. Synthesis and Chiral Recognition Ability of a Poly(phenylenevinylene)-Encapsulated Amylose Derivative Bull. Chem. Soc. Jpn. 2011, 84, 741-747 10.1246/bcsj.20110074
    • (2011) Bull. Chem. Soc. Jpn. , vol.84 , pp. 741-747
    • Tamura, K.1    Sam, N.S.M.2    Ikai, T.3    Okamoto, Y.4    Yashima, E.5
  • 222
    • 0002288520 scopus 로고
    • Tris(1-phenylethylcarbamate)s of Cellulose and Amylose as Useful Chiral Stationary Phases for Chromatographic Optical Resolution
    • Okamoto, Y.; Kaida, Y.; Hayashida, H.; Hatada, K. Tris(1-phenylethylcarbamate)s of Cellulose and Amylose as Useful Chiral Stationary Phases for Chromatographic Optical Resolution Chem. Lett. 1990, 909-912 10.1246/cl.1990.909
    • (1990) Chem. Lett. , pp. 909-912
    • Okamoto, Y.1    Kaida, Y.2    Hayashida, H.3    Hatada, K.4
  • 223
    • 0027315007 scopus 로고
    • Optical Resolution by High-Performance Liquid Chromatography on Benzylcarbamates of Cellulose and Amylose
    • Kaida, Y.; Okamoto, Y. Optical Resolution by High-Performance Liquid Chromatography on Benzylcarbamates of Cellulose and Amylose J. Chromatogr. 1993, 641, 267-278 10.1016/0021-9673(93)80143-V
    • (1993) J. Chromatogr. , vol.641 , pp. 267-278
    • Kaida, Y.1    Okamoto, Y.2
  • 224
    • 0002445850 scopus 로고
    • Tris(chloro- and methyl-disubstituted phenylcarbamate)s of Cellulose as Chiral Stationary Phases for Chromatographic Enantioseparation
    • Chankvetadze, B.; Yashima, E.; Okamoto, Y. Tris(chloro- and methyl-disubstituted phenylcarbamate)s of Cellulose as Chiral Stationary Phases for Chromatographic Enantioseparation Chem. Lett. 1993, 617-620 10.1246/cl.1993.617
    • (1993) Chem. Lett. , pp. 617-620
    • Chankvetadze, B.1    Yashima, E.2    Okamoto, Y.3
  • 225
    • 0028340483 scopus 로고
    • Chloromethylphenylcarbamate Derivatives of Cellulose as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Chankvetadze, B.; Yashima, E.; Okamoto, Y. Chloromethylphenylcarbamate Derivatives of Cellulose as Chiral Stationary Phases for High-Performance Liquid Chromatography J. Chromatogr. 1994, 670, 39-49 10.1016/0021-9673(94)80278-5
    • (1994) J. Chromatogr. , vol.670 , pp. 39-49
    • Chankvetadze, B.1    Yashima, E.2    Okamoto, Y.3
  • 226
    • 21844470446 scopus 로고    scopus 로고
    • Enantioseparation by HPLC Using Phenylcarbonate, Benzoylformate, p-Toluenesulfonylcarbamate, and Benzoylcarbamates of Cellulose and Amylose as Chiral Stationary Phases
    • Ikai, T.; Yamamoto, C.; Kamigaito, M.; Okamoto, Y. Enantioseparation by HPLC Using Phenylcarbonate, Benzoylformate, p-Toluenesulfonylcarbamate, and Benzoylcarbamates of Cellulose and Amylose as Chiral Stationary Phases Chirality 2005, 17, 299-304 10.1002/chir.20168
    • (2005) Chirality , vol.17 , pp. 299-304
    • Ikai, T.1    Yamamoto, C.2    Kamigaito, M.3    Okamoto, Y.4
  • 227
    • 0030731814 scopus 로고    scopus 로고
    • 3-Fluoro-, 3-Chloro- and 3-Bromo-5-methylphenylcarbamates of Cellulose and Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatographic Enantioseparation
    • Chankvetadze, B.; Chankvetadze, L.; Sidamonidze, S.; Kasashima, E.; Yashima, E.; Okamoto, Y. 3-Fluoro-, 3-Chloro- and 3-Bromo-5-methylphenylcarbamates of Cellulose and Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatographic Enantioseparation J. Chromatogr. A 1997, 787, 67-77 10.1016/S0021-9673(97)00648-1
    • (1997) J. Chromatogr. A , vol.787 , pp. 67-77
    • Chankvetadze, B.1    Chankvetadze, L.2    Sidamonidze, S.3    Kasashima, E.4    Yashima, E.5    Okamoto, Y.6
  • 228
    • 0027137495 scopus 로고
    • Resolution of Enantiomers by HPLC on Tris(4-alkoxyphenylcarbamate)s of Cellulose and Amylose
    • Okamoto, Y.; Ohashi, T.; Kaida, Y.; Yashima, E. Resolution of Enantiomers by HPLC on Tris(4-alkoxyphenylcarbamate)s of Cellulose and Amylose Chirality 1993, 5, 616-621 10.1002/chir.530050809
    • (1993) Chirality , vol.5 , pp. 616-621
    • Okamoto, Y.1    Ohashi, T.2    Kaida, Y.3    Yashima, E.4
  • 229
    • 33646190034 scopus 로고    scopus 로고
    • Enantioseparation Using Alkoxyphenylcarbamates of Cellulose and Amylose as Chiral Stationary Phase for High-Performance Liquid Chromatography
    • Yamamoto, C.; Inagaki, S.; Okamoto, Y. Enantioseparation Using Alkoxyphenylcarbamates of Cellulose and Amylose as Chiral Stationary Phase for High-Performance Liquid Chromatography J. Sep. Sci. 2006, 29, 915-923 10.1002/jssc.200500514
    • (2006) J. Sep. Sci. , vol.29 , pp. 915-923
    • Yamamoto, C.1    Inagaki, S.2    Okamoto, Y.3
  • 230
    • 84966145738 scopus 로고
    • Enantioseparation on Fluoro-Methylphenylcarbamates of Cellulose and Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Yashima, E.; Yamamoto, C.; Okamoto, Y. Enantioseparation on Fluoro-Methylphenylcarbamates of Cellulose and Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatography Polym. J. 1995, 27, 856-861 10.1295/polymj.27.856
    • (1995) Polym. J. , vol.27 , pp. 856-861
    • Yashima, E.1    Yamamoto, C.2    Okamoto, Y.3
  • 231
    • 0028935002 scopus 로고
    • Dimethyl-, Dichloro- and Chloromethylphenylcarbamates of Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Chankvetadze, B.; Yashima, E.; Okamoto, Y. Dimethyl-, Dichloro- and Chloromethylphenylcarbamates of Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatography J. Chromatogr. A 1995, 694, 101-109 10.1016/0021-9673(94)00729-S
    • (1995) J. Chromatogr. A , vol.694 , pp. 101-109
    • Chankvetadze, B.1    Yashima, E.2    Okamoto, Y.3
  • 232
    • 0003070479 scopus 로고
    • Tris(4-t-butylphenylcarbamate)s of Cellulose and Amylose as Useful Chiral Stationary Phases for Chromatographic Optical Resolution
    • Okamoto, Y.; Hatano, K.; Aburatani, R.; Hatada, K. Tris(4-t-butylphenylcarbamate)s of Cellulose and Amylose as Useful Chiral Stationary Phases for Chromatographic Optical Resolution Chem. Lett. 1989, 715-718 10.1246/cl.1989.715
    • (1989) Chem. Lett. , pp. 715-718
    • Okamoto, Y.1    Hatano, K.2    Aburatani, R.3    Hatada, K.4
  • 233
    • 0001990012 scopus 로고
    • "homogeneous" and "heterogeneous" Cellulose Tri-esters and a Cellulose Triurethane: Synthesis and Structural Investigations of the Crystalline State
    • Steinmeier, H.; Zugenmaier, P. "Homogeneous" and "Heterogeneous" Cellulose Tri-esters and a Cellulose Triurethane: Synthesis and Structural Investigations of the Crystalline State Carbohydr. Res. 1987, 164, 97-105 10.1016/0008-6215(87)80122-2
    • (1987) Carbohydr. Res. , vol.164 , pp. 97-105
    • Steinmeier, H.1    Zugenmaier, P.2
  • 234
    • 0022147876 scopus 로고
    • Structural Models for Some Liquid Crystalline Cellulose Derivatives
    • Vogt, U.; Zugenmaier, P. Ber. Bunsen-Ges. Structural Models for Some Liquid Crystalline Cellulose Derivatives Phys. Chem. 1985, 89, 1217-1224 10.1002/bbpc.19850891120
    • (1985) Phys. Chem. , vol.89 , pp. 1217-1224
    • Vogt, U.1    Zugenmaier, P.B.B.-G.2
  • 236
    • 84875527494 scopus 로고    scopus 로고
    • Enantioseparation Using ortho- or meta-Substituted Phenylcarbamates of Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Shen, J.; Zhao, Y.; Inagaki, S.; Yamamoto, C.; Shen, Y.; Liu, S.; Okamoto, Y. Enantioseparation Using ortho- or meta-Substituted Phenylcarbamates of Amylose as Chiral Stationary Phases for High-Performance Liquid Chromatography J. Chromatogr. A 2013, 1286, 41-46 10.1016/j.chroma.2013.02.020
    • (2013) J. Chromatogr. A , vol.1286 , pp. 41-46
    • Shen, J.1    Zhao, Y.2    Inagaki, S.3    Yamamoto, C.4    Shen, Y.5    Liu, S.6    Okamoto, Y.7
  • 239
    • 80051888226 scopus 로고    scopus 로고
    • Enantiomer Elution Order Reversal of Fluorenylmethoxycarbonyl-isoleucine in High-Performance Liquid Chromatography by Changing the Mobile Phase Temperature and Composition
    • Chankvetadze, L.; Ghibradze, N.; Karchkhadze, M.; Peng, L.; Farkas, T.; Chankvetadze, B. Enantiomer Elution Order Reversal of Fluorenylmethoxycarbonyl-isoleucine in High-Performance Liquid Chromatography by Changing the Mobile Phase Temperature and Composition J. Chromatogr. A 2011, 1218, 6554-6560 10.1016/j.chroma.2011.06.068
    • (2011) J. Chromatogr. A , vol.1218 , pp. 6554-6560
    • Chankvetadze, L.1    Ghibradze, N.2    Karchkhadze, M.3    Peng, L.4    Farkas, T.5    Chankvetadze, B.6
  • 240
    • 84904747309 scopus 로고    scopus 로고
    • Enantioseparation of Selected Chiral Sulfoxides in High-Performance Liquid Chromatography with Polysaccharide-based Chiral Selectors in Polar Organic Mobile Phases with Emphasis on Enantiomer Elution Order
    • Gegenava, M.; Chankvetadze, L.; Farkas, T.; Chankvetadze, B. Enantioseparation of Selected Chiral Sulfoxides in High-Performance Liquid Chromatography with Polysaccharide-based Chiral Selectors in Polar Organic Mobile Phases with Emphasis on Enantiomer Elution Order J. Sep. Sci. 2014, 37, 1083-1088 10.1002/jssc.201301318
    • (2014) J. Sep. Sci. , vol.37 , pp. 1083-1088
    • Gegenava, M.1    Chankvetadze, L.2    Farkas, T.3    Chankvetadze, B.4
  • 241
    • 84887159777 scopus 로고    scopus 로고
    • On the Effect of Basic and Acidic Additives on the Separation of the Enantiomers of Some Basic Drugs with Polysaccharide-based Chiral Selectors and Polar Organic Mobile Phases
    • Mosiashvili, L.; Chankvetadze, L.; Farkas, T.; Chankvetadze, B. On the Effect of Basic and Acidic Additives on the Separation of the Enantiomers of Some Basic Drugs with Polysaccharide-based Chiral Selectors and Polar Organic Mobile Phases J. Chromatogr. A 2013, 1317, 167-174 10.1016/j.chroma.2013.08.029
    • (2013) J. Chromatogr. A , vol.1317 , pp. 167-174
    • Mosiashvili, L.1    Chankvetadze, L.2    Farkas, T.3    Chankvetadze, B.4
  • 242
    • 84908083302 scopus 로고    scopus 로고
    • Effect of Content of Chiral Selector and Pore Size of Core-shell Type Silica Support on the Performance of Amylose Tris(3,5-dimethylphenylcarbamate)-based Chiral Stationary Phases in Nano-liquid Chromatography and Capillary Electrochromatography
    • Rocchi, S.; Fanali, S.; Farkas, T.; Chankvetadze, B. Effect of Content of Chiral Selector and Pore Size of Core-shell Type Silica Support on the Performance of Amylose Tris(3,5-dimethylphenylcarbamate)-based Chiral Stationary Phases in Nano-liquid Chromatography and Capillary Electrochromatography J. Chromatogr. A 2014, 1363, 363-371 10.1016/j.chroma.2014.05.029
    • (2014) J. Chromatogr. A , vol.1363 , pp. 363-371
    • Rocchi, S.1    Fanali, S.2    Farkas, T.3    Chankvetadze, B.4
  • 243
    • 74249114214 scopus 로고    scopus 로고
    • Systematic Evaluation of New Chiral Stationary Phases for Supercritical Fluid Chromatography Using a Standard Racemate Library
    • Pirzada, Z.; Personick, M.; Biba, M.; Gong, X.; Zhou, L.; Schafer, W.; Roussel, C.; Welch, C. J. Systematic Evaluation of New Chiral Stationary Phases for Supercritical Fluid Chromatography Using a Standard Racemate Library J. Chromatogr. A 2010, 1217, 1134-1138 10.1016/j.chroma.2009.10.004
    • (2010) J. Chromatogr. A , vol.1217 , pp. 1134-1138
    • Pirzada, Z.1    Personick, M.2    Biba, M.3    Gong, X.4    Zhou, L.5    Schafer, W.6    Roussel, C.7    Welch, C.J.8
  • 244
    • 43049084379 scopus 로고    scopus 로고
    • Enantiomer Resolution Screening Strategy Using Multiple Immobilised Polysaccharide-Based Chiral Stationary Phases
    • Zhang, T.; Nguyen, D.; Franco, P. Enantiomer Resolution Screening Strategy Using Multiple Immobilised Polysaccharide-Based Chiral Stationary Phases J. Chromatogr. A 2008, 1191, 214-222 10.1016/j.chroma.2007.12.026
    • (2008) J. Chromatogr. A , vol.1191 , pp. 214-222
    • Zhang, T.1    Nguyen, D.2    Franco, P.3
  • 246
    • 0035847289 scopus 로고    scopus 로고
    • Enantioseparations in Super- and Subcritical Fluid Chromatography
    • Terfloth, G. Enantioseparations in Super- and Subcritical Fluid Chromatography J. Chromatogr. A 2001, 906, 301-307 10.1016/S0021-9673(00)00952-3
    • (2001) J. Chromatogr. A , vol.906 , pp. 301-307
    • Terfloth, G.1
  • 247
    • 84892486150 scopus 로고    scopus 로고
    • Exploratory Data Analysis as a Tool for Similarity Assessment and Clustering of Chiral Polysaccharide-Based Systems Used to Separate Pharmaceuticals in Supercritical Fluid Chromatography
    • De Klerck, K.; Heyden, Y. V.; Mangelings, D. Exploratory Data Analysis as a Tool for Similarity Assessment and Clustering of Chiral Polysaccharide-Based Systems Used to Separate Pharmaceuticals in Supercritical Fluid Chromatography J. Chromatogr. A 2014, 1326, 110-124 10.1016/j.chroma.2013.12.052
    • (2014) J. Chromatogr. A , vol.1326 , pp. 110-124
    • De Klerck, K.1    Heyden, Y.V.2    Mangelings, D.3
  • 249
    • 0034794498 scopus 로고    scopus 로고
    • Effect of Organic Solvent, Electrolyte Salt and a Loading of Cellulose Tris(3,5-dichlorophenylcarbamate) on Silica Gel on Enantioseparation Characteristics in Capillary Electrochromatography
    • Chankvetadze, B.; Kartozia, I.; Breitkreutz, J.; Okamoto, Y.; Blaschke, G. Effect of Organic Solvent, Electrolyte Salt and a Loading of Cellulose Tris(3,5-dichlorophenylcarbamate) on Silica Gel on Enantioseparation Characteristics in Capillary Electrochromatography Electrophoresis 2001, 22, 3327-3334 10.1002/1522-2683(200109)22:153327::AID-ELPS33273.0.CO;2-J
    • (2001) Electrophoresis , vol.22 , pp. 3327-3334
    • Chankvetadze, B.1    Kartozia, I.2    Breitkreutz, J.3    Okamoto, Y.4    Blaschke, G.5
  • 250
    • 0034509301 scopus 로고    scopus 로고
    • Recent Progress in Enantiomer Separation by Capillary Electrochromatography
    • Wistuba, D.; Schurig, V. Recent Progress in Enantiomer Separation by Capillary Electrochromatography Electrophoresis 2000, 21, 4136-4158 10.1002/1522-2683(200012)21:184136::AID-ELPS41363.0.CO;2-1
    • (2000) Electrophoresis , vol.21 , pp. 4136-4158
    • Wistuba, D.1    Schurig, V.2
  • 251
    • 84858797788 scopus 로고    scopus 로고
    • Evaluation of New Cellulose-based Chiral Stationary Phases Sepapak-2 and Sepapak-4 for the Enantiomeric Separation of Pesticides by Nano Liquid Chromatography and Capillary Electrochromagraphy
    • Perez-Fernandez, V.; Dominguez-Vega, E.; Chankvetadze, B.; Crego, A. L.; Garcia, M. A.; Marina, M. L. Evaluation of New Cellulose-based Chiral Stationary Phases Sepapak-2 and Sepapak-4 for the Enantiomeric Separation of Pesticides by Nano Liquid Chromatography and Capillary Electrochromagraphy J. Chromatogr. A 2012, 1234, 22-31 10.1016/j.chroma.2012.01.035
    • (2012) J. Chromatogr. A , vol.1234 , pp. 22-31
    • Perez-Fernandez, V.1    Dominguez-Vega, E.2    Chankvetadze, B.3    Crego, A.L.4    Garcia, M.A.5    Marina, M.L.6
  • 252
    • 84917692556 scopus 로고    scopus 로고
    • Enantiomeric Separation of New Cathinone Derivatives Designer Drugs by Capillary Electrochromatography Using a Chiral Stationary Phase, Based on Amylose Tris(5-chloro-2-methylphenylcarbamate)
    • Aturki, Z.; Schmid, M. G.; Chankvetadze, B.; Fanali, S. Enantiomeric Separation of New Cathinone Derivatives Designer Drugs by Capillary Electrochromatography Using a Chiral Stationary Phase, Based on Amylose Tris(5-chloro-2-methylphenylcarbamate) Electrophoresis 2014, 35, 3242-3249 10.1002/elps.201400085
    • (2014) Electrophoresis , vol.35 , pp. 3242-3249
    • Aturki, Z.1    Schmid, M.G.2    Chankvetadze, B.3    Fanali, S.4
  • 253
    • 84906779538 scopus 로고    scopus 로고
    • Current Applications of Miniaturized Chromatographic and Electrophoretic Techniques in Drug Analysis
    • Aturki, Z.; Rocco, A.; Rocchi, S.; Fanali, S. Current Applications of Miniaturized Chromatographic and Electrophoretic Techniques in Drug Analysis J. Pharm. Biomed. Anal. 2014, 101, 194-220 10.1016/j.jpba.2014.03.041
    • (2014) J. Pharm. Biomed. Anal. , vol.101 , pp. 194-220
    • Aturki, Z.1    Rocco, A.2    Rocchi, S.3    Fanali, S.4
  • 254
    • 84889388808 scopus 로고    scopus 로고
    • 3 rd ed. Subramanian, G. Wiley: New York, Chapter 24
    • Abel, S.; Juza, M. In Chiral Separation Techniques, 3 rd ed.; Subramanian, G., Ed.; Wiley: New York, 2007; Chapter 24, pp 203-225.
    • (2007) Chiral Separation Techniques , pp. 203-225
    • Abel, S.1    Juza, M.2
  • 255
    • 0001427099 scopus 로고
    • Optical Resolution on Regioselectively Carbamoylated Cellulose and Amylose with 3,5-Dimethylphenyl and 3,5-Dichlorophenyl Isocyanates
    • Kaida, Y.; Okamoto, Y. Optical Resolution on Regioselectively Carbamoylated Cellulose and Amylose with 3,5-Dimethylphenyl and 3,5-Dichlorophenyl Isocyanates Bull. Chem. Soc. Jpn. 1993, 66, 2225-2232 10.1246/bcsj.66.2225
    • (1993) Bull. Chem. Soc. Jpn. , vol.66 , pp. 2225-2232
    • Kaida, Y.1    Okamoto, Y.2
  • 256
    • 0035847234 scopus 로고    scopus 로고
    • Regioselectively Modified Polysaccharide Derivatives as Chiral Stationary Phases in High-Performance Liquid Chromatography
    • Felix, G. Regioselectively Modified Polysaccharide Derivatives as Chiral Stationary Phases in High-Performance Liquid Chromatography J. Chromatogr. A 2001, 906, 171-184 10.1016/S0021-9673(00)00943-2
    • (2001) J. Chromatogr. A , vol.906 , pp. 171-184
    • Felix, G.1
  • 257
    • 0006638706 scopus 로고
    • Effets Moléculaires et Supramoléculaires en Chromatographie sur Phases Stationnaires Chirales aÌ€ Base de Cellulose
    • Francotte, E.; Zhang, T. Effets Moléculaires et Supramoléculaires en Chromatographie sur Phases Stationnaires Chirales aÌ€ Base de Cellulose Anal. Mag. 1995, 23, M13-M16
    • (1995) Anal. Mag. , vol.23 , pp. M13-M16
    • Francotte, E.1    Zhang, T.2
  • 258
    • 2942657581 scopus 로고    scopus 로고
    • A Straight Way to Regioselectively Functionalized Polysaccharide Esters
    • Dicke, R. A Straight Way to Regioselectively Functionalized Polysaccharide Esters Cellulose 2004, 11, 255-263 10.1023/B:CELL.0000025426.82260.71
    • (2004) Cellulose , vol.11 , pp. 255-263
    • Dicke, R.1
  • 259
    • 45449083892 scopus 로고    scopus 로고
    • Synthesis and Chiral Recognition of Novel Regioselectively Substituted Amylose Derivatives
    • Kondo, S.; Yamamoto, C.; Kamigaito, M.; Okamoto, Y. Synthesis and Chiral Recognition of Novel Regioselectively Substituted Amylose Derivatives Chem. Lett. 2008, 37, 558-559 10.1246/cl.2008.558
    • (2008) Chem. Lett. , vol.37 , pp. 558-559
    • Kondo, S.1    Yamamoto, C.2    Kamigaito, M.3    Okamoto, Y.4
  • 260
    • 0028129155 scopus 로고
    • 3,5-Dimethylphenylcarbamates of Cellulose and Amylose Regioselectively Bonded to Silica Gel as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Yashima, E.; Fukaya, S.; Okamoto, Y. 3,5-Dimethylphenylcarbamates of Cellulose and Amylose Regioselectively Bonded to Silica Gel as Chiral Stationary Phases for High-Performance Liquid Chromatography J. Chromatogr. A 1994, 677, 11-19 10.1016/0021-9673(94)80539-3
    • (1994) J. Chromatogr. A , vol.677 , pp. 11-19
    • Yashima, E.1    Fukaya, S.2    Okamoto, Y.3
  • 261
    • 74049154230 scopus 로고    scopus 로고
    • Synthesis and Chiral Recognition of Novel Amylose Derivatives Containing Regioselectively Benzoate and Phenylcarbamate Groups
    • Shen, J.; Ikai, T.; Okamoto, Y. Synthesis and Chiral Recognition of Novel Amylose Derivatives Containing Regioselectively Benzoate and Phenylcarbamate Groups J. Chromatogr. A 2010, 1217, 1041-1047 10.1016/j.chroma.2009.07.027
    • (2010) J. Chromatogr. A , vol.1217 , pp. 1041-1047
    • Shen, J.1    Ikai, T.2    Okamoto, Y.3
  • 262
    • 81755186871 scopus 로고    scopus 로고
    • Controlled Immobilization of Polysaccharide Derivatives for Efficient Chiral Separation
    • Okamoto, Y.; Ikai, T.; Shen, J. Controlled Immobilization of Polysaccharide Derivatives for Efficient Chiral Separation Isr. J. Chem. 2011, 51, 1096-1106 10.1002/ijch.201100025
    • (2011) Isr. J. Chem. , vol.51 , pp. 1096-1106
    • Okamoto, Y.1    Ikai, T.2    Shen, J.3
  • 263
    • 30744452726 scopus 로고    scopus 로고
    • Cellulose 3,5-Dimethylphenylcarbamate Immobilized on Silica: A New Chiral Stationary Phase for the Analysis of Enantiomers
    • Zhang, T.; Nguyen, D.; Franco, P.; Murakami, T.; Ohnishi, A.; Kurosawa, H. Cellulose 3,5-Dimethylphenylcarbamate Immobilized on Silica: A New Chiral Stationary Phase for the Analysis of Enantiomers Anal. Chim. Acta 2006, 557, 221-228 10.1016/j.aca.2005.10.017
    • (2006) Anal. Chim. Acta , vol.557 , pp. 221-228
    • Zhang, T.1    Nguyen, D.2    Franco, P.3    Murakami, T.4    Ohnishi, A.5    Kurosawa, H.6
  • 264
    • 40849087856 scopus 로고    scopus 로고
    • Cellulose Tris(3,5-dichlorophenylcarbamate) Immobilized on Silica: A Novel Chiral Stationary Phase for Resolution of Enantiomers
    • Zhang, T.; Nguyen, D.; Franco, P.; Isobe, Y.; Michishita, T.; Murakami, T. Cellulose Tris(3,5-dichlorophenylcarbamate) Immobilized on Silica: A Novel Chiral Stationary Phase for Resolution of Enantiomers J. Pharm. Biomed. Anal. 2008, 46, 882-891 10.1016/j.jpba.2007.06.008
    • (2008) J. Pharm. Biomed. Anal. , vol.46 , pp. 882-891
    • Zhang, T.1    Nguyen, D.2    Franco, P.3    Isobe, Y.4    Michishita, T.5    Murakami, T.6
  • 265
    • 0032767528 scopus 로고    scopus 로고
    • Computational Studies on Chiral Discrimination Mechanism of Phenylcarbamate Derivatives of Cellulose
    • Yamamoto, C.; Yashima, E.; Okamoto, Y. Computational Studies on Chiral Discrimination Mechanism of Phenylcarbamate Derivatives of Cellulose Bull. Chem. Soc. Jpn. 1999, 72, 1815-1825 10.1246/bcsj.72.1815
    • (1999) Bull. Chem. Soc. Jpn. , vol.72 , pp. 1815-1825
    • Yamamoto, C.1    Yashima, E.2    Okamoto, Y.3
  • 266
    • 0035613277 scopus 로고    scopus 로고
    • Cellulose 3,5-Dimethylphenylcarbamate Immobilized onto Silica Gel Via Copolymerization with a Vinyl Monomer and Its Chiral Recognition Ability as a Chiral Stationary Phase for HPLC
    • Kubota, T.; Kusano, C.; Yamamoto, C.; Yashima, E.; Okamoto, Y. Cellulose 3,5-Dimethylphenylcarbamate Immobilized onto Silica Gel Via Copolymerization with a Vinyl Monomer and Its Chiral Recognition Ability as a Chiral Stationary Phase for HPLC Chem. Lett. 2001, 30, 724-725 10.1246/cl.2001.724
    • (2001) Chem. Lett. , vol.30 , pp. 724-725
    • Kubota, T.1    Kusano, C.2    Yamamoto, C.3    Yashima, E.4    Okamoto, Y.5
  • 267
    • 0242524452 scopus 로고    scopus 로고
    • Preparation and Chiral Recognition Ability of Cellulose 3,5-Dimethylphenylcarbamate Immobilized on Silica Gel through Radical Polymerization
    • Kubota, T.; Yamamoto, C.; Okamoto, Y. Preparation and Chiral Recognition Ability of Cellulose 3,5-Dimethylphenylcarbamate Immobilized on Silica Gel through Radical Polymerization J. Polym. Sci., Part A: Polym. Chem. 2003, 41, 3703-3712 10.1002/pola.10836
    • (2003) J. Polym. Sci., Part A: Polym. Chem. , vol.41 , pp. 3703-3712
    • Kubota, T.1    Yamamoto, C.2    Okamoto, Y.3
  • 268
    • 34250701189 scopus 로고    scopus 로고
    • Immobilization of Polysaccharide Derivatives onto Silica Gel. Facile Synthesis of Chiral Packing Materials by Means of Intermolecular Polycondensation of Triethoxysilyl Groups
    • Ikai, T.; Yamamoto, C.; Kamigaito, M.; Okamoto, Y. Immobilization of Polysaccharide Derivatives onto Silica Gel. Facile Synthesis of Chiral Packing Materials by Means of Intermolecular Polycondensation of Triethoxysilyl Groups J. Chromatogr. A 2007, 1157, 151-158 10.1016/j.chroma.2007.04.054
    • (2007) J. Chromatogr. A , vol.1157 , pp. 151-158
    • Ikai, T.1    Yamamoto, C.2    Kamigaito, M.3    Okamoto, Y.4
  • 269
    • 0030222508 scopus 로고    scopus 로고
    • Preparation of Silica Gel-Bonded Amylose through Enzyme-Catalyzed Polymerization and Chiral Recognition Ability of Its Phenylcarbamate Derivative in HPLC
    • Enomoto, N.; Furukawa, S.; Ogasawara, Y.; Akano, H.; Kawamura, Y.; Yashima, E.; Okamoto, Y. Preparation of Silica Gel-Bonded Amylose through Enzyme-Catalyzed Polymerization and Chiral Recognition Ability of Its Phenylcarbamate Derivative in HPLC Anal. Chem. 1996, 68, 2798-2804 10.1021/ac960002v
    • (1996) Anal. Chem. , vol.68 , pp. 2798-2804
    • Enomoto, N.1    Furukawa, S.2    Ogasawara, Y.3    Akano, H.4    Kawamura, Y.5    Yashima, E.6    Okamoto, Y.7
  • 270
    • 0020007081 scopus 로고
    • Study on Polysaccharide by the Fluorescence Method II. Micro-Brownian Motion and Conformational Change of Amylose in Aqueous Solution
    • Kitamura, S.; Yonokawa, H.; Mitsuie, S.; Kuge, T. Study on Polysaccharide by the Fluorescence Method II. Micro-Brownian Motion and Conformational Change of Amylose in Aqueous Solution Polym. J. 1982, 14, 93-99 10.1295/polymj.14.93
    • (1982) Polym. J. , vol.14 , pp. 93-99
    • Kitamura, S.1    Yonokawa, H.2    Mitsuie, S.3    Kuge, T.4
  • 271
    • 0027602524 scopus 로고
    • Chemically Bonded Chiral Stationary Phase Prepared by the Polymerization of Cellulose P-Vinylbenzoate
    • Kimata, K.; Tsuboi, R.; Hosoya, K.; Tanaka, N. Chemically Bonded Chiral Stationary Phase Prepared by the Polymerization of Cellulose P-Vinylbenzoate Anal. Methods Instrum. 1993, 1, 23-29
    • (1993) Anal. Methods Instrum. , vol.1 , pp. 23-29
    • Kimata, K.1    Tsuboi, R.2    Hosoya, K.3    Tanaka, N.4
  • 272
    • 0037216592 scopus 로고    scopus 로고
    • Preparation of Chiral Stationary Phase for HPLC Based on Immobilization of Cellulose 3,5-Dimethylphenylcarbamate Derivatives on Silica Gel
    • Kubota, T.; Yamamoto, C.; Okamoto, Y. Preparation of Chiral Stationary Phase for HPLC Based on Immobilization of Cellulose 3,5-Dimethylphenylcarbamate Derivatives on Silica Gel Chirality 2003, 15, 77-82 10.1002/chir.10169
    • (2003) Chirality , vol.15 , pp. 77-82
    • Kubota, T.1    Yamamoto, C.2    Okamoto, Y.3
  • 273
    • 0035847278 scopus 로고    scopus 로고
    • Covalently Bonded Polysaccharide Derivatives as Chiral Stationary Phases in High-Performance Liquid Chromatography
    • Franco, P.; Senso, A.; Oliveros, L.; Minguillón, C. Covalently Bonded Polysaccharide Derivatives as Chiral Stationary Phases in High-Performance Liquid Chromatography J. Chromatogr. A 2001, 906, 155-170 10.1016/S0021-9673(00)00531-8
    • (2001) J. Chromatogr. A , vol.906 , pp. 155-170
    • Franco, P.1    Senso, A.2    Oliveros, L.3    Minguillón, C.4
  • 274
    • 0028898101 scopus 로고
    • Chiral Chromatographic Discrimination Ability of a Cellulose 3,5-Dimethylphenylcarbamate/10-Undecenoate Mixed Derivative Fixed on Several Chromatographic Matrices
    • Oliveros, L.; López, P.; Minguillón, C.; Franco, P. Chiral Chromatographic Discrimination Ability of a Cellulose 3,5-Dimethylphenylcarbamate/10-Undecenoate Mixed Derivative Fixed on Several Chromatographic Matrices J. Liq. Chromatogr. 1995, 18, 1521-1532 10.1080/10826079508009292
    • (1995) J. Liq. Chromatogr. , vol.18 , pp. 1521-1532
    • Oliveros, L.1    López, P.2    Minguillón, C.3    Franco, P.4
  • 275
    • 0029901310 scopus 로고    scopus 로고
    • Bonded Cellulose-Derived High-Performance Liquid Chromatography Chiral Stationary Phases: I. Influence of the Degree of Fixation on Selectivity
    • Minguillón, C.; Franco, P.; Oliveros, L.; López, P. Bonded Cellulose-Derived High-Performance Liquid Chromatography Chiral Stationary Phases: I. Influence of the Degree of Fixation on Selectivity J. Chromatogr. A 1996, 728, 407-414 10.1016/0021-9673(95)01123-4
    • (1996) J. Chromatogr. A , vol.728 , pp. 407-414
    • Minguillón, C.1    Franco, P.2    Oliveros, L.3    López, P.4
  • 276
    • 0037414548 scopus 로고    scopus 로고
    • Mixed Cellulose-Derived Benzoates Bonded on Allyl Silica Gel as HPLC Chiral Stationary Phases: Influence of the Introduction of an Aromatic Moiety in the Fixation Substituent
    • Garcés, J.; Franco, P.; Oliveros, L.; Minguillón, C. Mixed Cellulose-Derived Benzoates Bonded on Allyl Silica Gel as HPLC Chiral Stationary Phases: Influence of the Introduction of an Aromatic Moiety in the Fixation Substituent Tetrahedron: Asymmetry 2003, 14, 1179-1185 10.1016/S0957-4166(03)00176-9
    • (2003) Tetrahedron: Asymmetry , vol.14 , pp. 1179-1185
    • Garcés, J.1    Franco, P.2    Oliveros, L.3    Minguillón, C.4
  • 277
    • 0032548911 scopus 로고    scopus 로고
    • 3,5-Dimethylphenylcarbamates of Amylose, Chitosan and Cellulose Bonded on Silica Gel Comparison of Their Chiral Recognition Abilities of High-Performance Liquid Chromatography Chiral Stationary Phases
    • Franco, P.; Senso, A.; Minguillón, C.; Oliveros, L. 3,5-Dimethylphenylcarbamates of Amylose, Chitosan and Cellulose Bonded on Silica Gel Comparison of Their Chiral Recognition Abilities of High-Performance Liquid Chromatography Chiral Stationary Phases J. Chromatogr. A 1998, 796, 265-272 10.1016/S0021-9673(97)01004-2
    • (1998) J. Chromatogr. A , vol.796 , pp. 265-272
    • Franco, P.1    Senso, A.2    Minguillón, C.3    Oliveros, L.4
  • 278
    • 0032892811 scopus 로고    scopus 로고
    • Chitosan Derivatives as Chiral Selectors Bonded on Allyl Silica Gel: Preparation, Characterisation and Study of the Resulting High-Performance Liquid Chromatography Chiral Stationary Phases
    • Senso, A.; Oliveros, L.; Minguillón, C. Chitosan Derivatives as Chiral Selectors Bonded on Allyl Silica Gel: Preparation, Characterisation and Study of the Resulting High-Performance Liquid Chromatography Chiral Stationary Phases J. Chromatogr. A 1999, 839, 15-21 10.1016/S0021-9673(99)00072-2
    • (1999) J. Chromatogr. A , vol.839 , pp. 15-21
    • Senso, A.1    Oliveros, L.2    Minguillón, C.3
  • 279
    • 4544275995 scopus 로고    scopus 로고
    • Phenylcarbamate Derivatives of Cellulose and Amylose Immobilized onto Silica Gel as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Kubota, T.; Yamamoto, C.; Okamoto, Y. Phenylcarbamate Derivatives of Cellulose and Amylose Immobilized onto Silica Gel as Chiral Stationary Phases for High-Performance Liquid Chromatography J. Polym. Sci., Part A: Polym. Chem. 2004, 42, 4704-4710 10.1002/pola.20372
    • (2004) J. Polym. Sci., Part A: Polym. Chem. , vol.42 , pp. 4704-4710
    • Kubota, T.1    Yamamoto, C.2    Okamoto, Y.3
  • 280
    • 33746419558 scopus 로고    scopus 로고
    • One-pot Synthesis of Polysaccharide 3,5-Dimethylphenylcarbamates Having a Random Vinyl Group for Immobilization on Silica Gel as Chiral Stationary Phases
    • Chen, X.; Yamamoto, C.; Okamoto, Y. One-pot Synthesis of Polysaccharide 3,5-Dimethylphenylcarbamates Having a Random Vinyl Group for Immobilization on Silica Gel as Chiral Stationary Phases J. Sep. Sci. 2006, 29, 1432-1439 10.1002/jssc.200600006
    • (2006) J. Sep. Sci. , vol.29 , pp. 1432-1439
    • Chen, X.1    Yamamoto, C.2    Okamoto, Y.3
  • 281
    • 0037080865 scopus 로고    scopus 로고
    • Immobilized Halogenophenylcarbamate Derivatives of Cellulose as Novel Stationary Phases for Enantioselective Drug Analysis
    • Francotte, E.; Huynh, D. Immobilized Halogenophenylcarbamate Derivatives of Cellulose as Novel Stationary Phases for Enantioselective Drug Analysis J. Pharm. Biomed. Anal. 2002, 27, 421-429 10.1016/S0731-7085(01)00568-4
    • (2002) J. Pharm. Biomed. Anal. , vol.27 , pp. 421-429
    • Francotte, E.1    Huynh, D.2
  • 282
    • 0034646847 scopus 로고    scopus 로고
    • Separation of Enantiomers by Packed Capillary Electrochromatography on a Cellulose-based Stationary Phase
    • Mayer, S.; Briand, X.; Francotte, E. Separation of Enantiomers by Packed Capillary Electrochromatography on a Cellulose-based Stationary Phase J. Chromatogr. A 2000, 875, 331-339 10.1016/S0021-9673(99)01335-7
    • (2000) J. Chromatogr. A , vol.875 , pp. 331-339
    • Mayer, S.1    Briand, X.2    Francotte, E.3
  • 283
    • 3042569129 scopus 로고    scopus 로고
    • High-Performance Liquid Chromatographic Enantioseparations on Monolithic Silica Columns Containing a Covalently Attached 3,5-Dimethylphenylcarbamate Derivative of Cellulose
    • Chankvetadze, B.; Ikai, T.; Yamamoto, C.; Okamoto, Y. High-Performance Liquid Chromatographic Enantioseparations on Monolithic Silica Columns Containing a Covalently Attached 3,5-Dimethylphenylcarbamate Derivative of Cellulose J. Chromatogr. A 2004, 1042, 55-60 10.1016/j.chroma.2004.05.011
    • (2004) J. Chromatogr. A , vol.1042 , pp. 55-60
    • Chankvetadze, B.1    Ikai, T.2    Yamamoto, C.3    Okamoto, Y.4
  • 284
    • 34347325034 scopus 로고    scopus 로고
    • Chemical Immobilization of Azido Cellulose Phenylcarbamate onto Silica Gel Via Staudinger Reaction and Its Application as a Chiral Stationary Phase for HPLC
    • Zhang, S.; Ong, T.-T.; Ng, S.-C.; Chan, H. S. O. Chemical Immobilization of Azido Cellulose Phenylcarbamate onto Silica Gel Via Staudinger Reaction and Its Application as a Chiral Stationary Phase for HPLC Tetrahedron Lett. 2007, 48, 5487-5490 10.1016/j.tetlet.2007.05.167
    • (2007) Tetrahedron Lett. , vol.48 , pp. 5487-5490
    • Zhang, S.1    Ong, T.-T.2    Ng, S.-C.3    Chan, H.S.O.4
  • 285
    • 33846683607 scopus 로고    scopus 로고
    • Efficient Immobilization of Cellulose Phenylcarbamate Bearing Alkoxysilyl Group onto Silica Gel by Intermolecular Polycondensation and Its Chiral Recognition
    • Ikai, T.; Yamamoto, C.; Kamigaito, M.; Okamoto, Y. Efficient Immobilization of Cellulose Phenylcarbamate Bearing Alkoxysilyl Group onto Silica Gel by Intermolecular Polycondensation and Its Chiral Recognition Chem. Lett. 2006, 35, 1250-1251 10.1246/cl.2006.1250
    • (2006) Chem. Lett. , vol.35 , pp. 1250-1251
    • Ikai, T.1    Yamamoto, C.2    Kamigaito, M.3    Okamoto, Y.4
  • 286
    • 0043159059 scopus 로고    scopus 로고
    • Synthesis of Covalently Bonded Cellulose Derivative Chiral Stationary Phases with a Bifunctional Reagent of 3-(Triethoxysilyl)propyl Isocyanate
    • Chen, X.; Liu, Y.; Kong, L.; Zou, H. Synthesis of Covalently Bonded Cellulose Derivative Chiral Stationary Phases with a Bifunctional Reagent of 3-(Triethoxysilyl)propyl Isocyanate J. Chromatogr. A 2003, 1010, 185-194 10.1016/S0021-9673(03)01104-X
    • (2003) J. Chromatogr. A , vol.1010 , pp. 185-194
    • Chen, X.1    Liu, Y.2    Kong, L.3    Zou, H.4
  • 287
    • 0033816664 scopus 로고    scopus 로고
    • Chiral Dendrophanes, Dendro[2]rotaxanes, and Dendro[2]catenanes: Synthesis and Chiroptical Phenomena
    • Reuter, C.; Pawlittzki, G.; Wörsdörfer, U.; Plevoets, M.; Mohry, A.; Kubota, T.; Okamoto, Y.; Vögtle, F. Chiral Dendrophanes, Dendro[2]rotaxanes, and Dendro[2]catenanes: Synthesis and Chiroptical Phenomena Eur. J. Org. Chem. 2000, 2000, 3059-3067 10.1002/1099-0690(200009)2000:173059::AID-EJOC30593.0.CO;2-T
    • (2000) Eur. J. Org. Chem. , vol.2000 , pp. 3059-3067
    • Reuter, C.1    Pawlittzki, G.2    Wörsdörfer, U.3    Plevoets, M.4    Mohry, A.5    Kubota, T.6    Okamoto, Y.7    Vögtle, F.8
  • 288
  • 289
    • 0037020281 scopus 로고    scopus 로고
    • Dendronized Molecular Knots: Selective Synthesis of Various Generations, Enantiomer Separation, Circular Dichroism
    • Recker, J.; Müller, W. M.; Müller, U.; Kubota, T.; Okamoto, Y.; Nieger, M.; Vögtle, F. Dendronized Molecular Knots: Selective Synthesis of Various Generations, Enantiomer Separation, Circular Dichroism Chem.-Eur. J. 2002, 8, 4434-4442 10.1002/1521-3765(20021004)8:194434::AID-CHEM44343.0.CO;2-#
    • (2002) Chem. - Eur. J. , vol.8 , pp. 4434-4442
    • Recker, J.1    Müller, W.M.2    Müller, U.3    Kubota, T.4    Okamoto, Y.5    Nieger, M.6    Vögtle, F.7
  • 291
    • 21544460981 scopus 로고    scopus 로고
    • Optimization of the Chiral Separation of a Ca-Sensitizing Drug on an Immobilized Polysaccharide-Based Chiral Stationary Phase: Case Study with a Preparative Perspective
    • Zhang, T.; Scaeffer, M.; Franco, P. Optimization of the Chiral Separation of a Ca-Sensitizing Drug on an Immobilized Polysaccharide-Based Chiral Stationary Phase: Case Study with a Preparative Perspective J. Chromatogr. A 2005, 1083, 96-101 10.1016/j.chroma.2005.06.003
    • (2005) J. Chromatogr. A , vol.1083 , pp. 96-101
    • Zhang, T.1    Scaeffer, M.2    Franco, P.3
  • 292
    • 77955415067 scopus 로고    scopus 로고
    • Application of an Immobilised Amylose-Based Chiral Stationary Phase to the Development of New Monoamine Oxidase B Inhibitors
    • Sanna, M. L.; Maccioni, E.; Vigo, S.; Faggi, C.; Cirilli, R. Application of an Immobilised Amylose-Based Chiral Stationary Phase to the Development of New Monoamine Oxidase B Inhibitors Talanta 2010, 82, 426-431 10.1016/j.talanta.2010.04.039
    • (2010) Talanta , vol.82 , pp. 426-431
    • Sanna, M.L.1    Maccioni, E.2    Vigo, S.3    Faggi, C.4    Cirilli, R.5
  • 293
    • 28944433830 scopus 로고    scopus 로고
    • Analytical and Semipreparative High Performance Liquid Chromatography Enantioseparation of New Substituted 1-Thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-Pyrazoles on Polysaccharide-based Chiral Stationary Phases in Normal-phase, Polar Organic and Reversed-phase Conditions
    • Cirilli, R.; Simonelli, A.; Ferretti, R.; Bolasco, A.; Chimenti, P.; Secci, D.; Maccioni, E.; Scci, D.; Maccioni, E.; Torre, F. L. Analytical and Semipreparative High Performance Liquid Chromatography Enantioseparation of New Substituted 1-Thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)-Pyrazoles on Polysaccharide-based Chiral Stationary Phases in Normal-phase, Polar Organic and Reversed-phase Conditions J. Chromatogr. A 2006, 1101, 198-203 10.1016/j.chroma.2005.10.003
    • (2006) J. Chromatogr. A , vol.1101 , pp. 198-203
    • Cirilli, R.1    Simonelli, A.2    Ferretti, R.3    Bolasco, A.4    Chimenti, P.5    Secci, D.6    Maccioni, E.7    Scci, D.8    Maccioni, E.9    Torre, F.L.10
  • 294
    • 84858681579 scopus 로고    scopus 로고
    • Asymmetric Synthesis of (Triaryl)methylamines by Rhodium-Catalyzed Addition of Arylboroxines to Cyclic N-Sulfonyl Ketimines
    • Nishimura, T.; Noishiki, A.; Tsui, G. C.; Hayashi, T. Asymmetric Synthesis of (Triaryl)methylamines by Rhodium-Catalyzed Addition of Arylboroxines to Cyclic N-Sulfonyl Ketimines J. Am. Chem. Soc. 2012, 134, 5056-5059 10.1021/ja300697c
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 5056-5059
    • Nishimura, T.1    Noishiki, A.2    Tsui, G.C.3    Hayashi, T.4
  • 295
    • 54349101567 scopus 로고    scopus 로고
    • Analytical and Semi-Preparative Enantioseparation of Organic Phosphonates on a New Immobilized Amylose Based Chiral Stationary Phase
    • Zhang, Y.; Song, B.; Bhadury, P. S.; Hu, D.; Yang, S.; Shi, X.; Liu, D.; Jin, L. Analytical and Semi-Preparative Enantioseparation of Organic Phosphonates on a New Immobilized Amylose Based Chiral Stationary Phase J. Sep. Sci. 2008, 31, 2946-2952 10.1002/jssc.200800270
    • (2008) J. Sep. Sci. , vol.31 , pp. 2946-2952
    • Zhang, Y.1    Song, B.2    Bhadury, P.S.3    Hu, D.4    Yang, S.5    Shi, X.6    Liu, D.7    Jin, L.8
  • 296
    • 33750071730 scopus 로고    scopus 로고
    • Direct HPLC Enantioseparation of Chiral Aptazepine Derivatives on Coated and Immobilized Polysaccharide-Based Chiral Stationary Phases
    • Cirilli, R.; Orlando, V.; Ferretti, R.; Turchetto, L.; Silvestri, R.; Martino, G. D.; Torre, F. L. Direct HPLC Enantioseparation of Chiral Aptazepine Derivatives on Coated and Immobilized Polysaccharide-Based Chiral Stationary Phases Chirality 2006, 18, 621-632 10.1002/chir.20298
    • (2006) Chirality , vol.18 , pp. 621-632
    • Cirilli, R.1    Orlando, V.2    Ferretti, R.3    Turchetto, L.4    Silvestri, R.5    Martino, G.D.6    Torre, F.L.7
  • 297
    • 37149039513 scopus 로고    scopus 로고
    • High-Performance Liquid Chromatography Enantioseparation of Proton Pump Inhibitors Using the Immobilized Amylose-Based Chiralpak IA Chiral Stationary Phase in Normal-phase, Polar Organic and Reversed-phase Conditions
    • Cirilli, R.; Ferretti, R.; Gallinella, B.; Santis, E. D.; Zanitti, L.; Torre, F. L. High-Performance Liquid Chromatography Enantioseparation of Proton Pump Inhibitors Using the Immobilized Amylose-Based Chiralpak IA Chiral Stationary Phase in Normal-phase, Polar Organic and Reversed-phase Conditions J. Chromatogr. A 2008, 1177, 105-113 10.1016/j.chroma.2007.11.027
    • (2008) J. Chromatogr. A , vol.1177 , pp. 105-113
    • Cirilli, R.1    Ferretti, R.2    Gallinella, B.3    Santis, E.D.4    Zanitti, L.5    Torre, F.L.6
  • 299
    • 84863229904 scopus 로고    scopus 로고
    • Rhodium-catalyzed Enantioselective Synthesis, Crystal Structures, and Photophysical Properties of Helically Chiral 1,1′-Bitriphenylenes
    • Sawada, Y.; Furumi, S.; Takai, A.; Takeuchi, M.; Noguchi, K.; Tanaka, K. Rhodium-catalyzed Enantioselective Synthesis, Crystal Structures, and Photophysical Properties of Helically Chiral 1,1′-Bitriphenylenes J. Am. Chem. Soc. 2012, 134, 4080-4083 10.1021/ja300278e
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 4080-4083
    • Sawada, Y.1    Furumi, S.2    Takai, A.3    Takeuchi, M.4    Noguchi, K.5    Tanaka, K.6
  • 300
    • 66649134677 scopus 로고    scopus 로고
    • Temperature-Induced Inversion of Elution Order in the Chromatographic Enantioseparation of 1,1′-Bi-2-naphthol on an Immobilized Polysaccharide-Based Chiral Stationary Phase
    • Yao, B.; Zhan, F.; Yu, G.; Chen, Z.; Fan, W.; Zeng, X.; Zeng, Q.; Weng, W. Temperature-Induced Inversion of Elution Order in the Chromatographic Enantioseparation of 1,1′-Bi-2-naphthol on an Immobilized Polysaccharide-Based Chiral Stationary Phase J. Chromatogr. A 2009, 1216, 5429-5435 10.1016/j.chroma.2009.05.032
    • (2009) J. Chromatogr. A , vol.1216 , pp. 5429-5435
    • Yao, B.1    Zhan, F.2    Yu, G.3    Chen, Z.4    Fan, W.5    Zeng, X.6    Zeng, Q.7    Weng, W.8
  • 301
    • 54249131552 scopus 로고    scopus 로고
    • Chromatographic Enantioseparations of Binaphthyl Compounds on an Immobilized Polysaccharide-Based Chiral Stationary Phase
    • Weng, W.; Guo, H.; Zhan, F.; Fang, H.; Wang, Q.; Yao, B.; Li, S. Chromatographic Enantioseparations of Binaphthyl Compounds on an Immobilized Polysaccharide-Based Chiral Stationary Phase J. Chromatogr. A 2008, 1210, 178-184 10.1016/j.chroma.2008.09.048
    • (2008) J. Chromatogr. A , vol.1210 , pp. 178-184
    • Weng, W.1    Guo, H.2    Zhan, F.3    Fang, H.4    Wang, Q.5    Yao, B.6    Li, S.7
  • 303
    • 33746470231 scopus 로고    scopus 로고
    • Analytical and Semipreparative High Performance Liquid Chromatography Separation of Stereoisomers of Novel 3,4-Dihydropyrimidin-4(3H)-one Derivatives on the Immobilised Amylose-Based Chiralpak IA Chiral Stationary Phase
    • Cirilli, R.; Ferretti, R.; Gallinella, B.; Torre, F. L.; Mai, A.; Rotili, D. Analytical and Semipreparative High Performance Liquid Chromatography Separation of Stereoisomers of Novel 3,4-Dihydropyrimidin-4(3H)-one Derivatives on the Immobilised Amylose-Based Chiralpak IA Chiral Stationary Phase J. Sep. Sci. 2006, 29, 1399-1406 10.1002/jssc.200600019
    • (2006) J. Sep. Sci. , vol.29 , pp. 1399-1406
    • Cirilli, R.1    Ferretti, R.2    Gallinella, B.3    Torre, F.L.4    Mai, A.5    Rotili, D.6
  • 304
    • 48349137591 scopus 로고    scopus 로고
    • A Validated LC Method for Determination of the Enantiomeric Purity of Montelukast Sodium in Bulk Drug Samples and Pharmaceutical Dosage Forms
    • Radhakrishnanand, P.; Subba Rao, D. V.; Surendranath, K. V.; Subrahmanyam, D. A Validated LC Method for Determination of the Enantiomeric Purity of Montelukast Sodium in Bulk Drug Samples and Pharmaceutical Dosage Forms Chromatographia 2008, 68, 263-267 10.1365/s10337-008-0684-5
    • (2008) Chromatographia , vol.68 , pp. 263-267
    • Radhakrishnanand, P.1    Subba Rao, D.V.2    Surendranath, K.V.3    Subrahmanyam, D.4
  • 305
    • 84856295370 scopus 로고    scopus 로고
    • Thionium Ion Initiated Medium-Sized Ring Formation: the Total Synthesis of Asteriscunolide D
    • Trost, B. M.; Burns, A. C.; Bartlett, M. J.; Tautz, T.; Weiss, A. H. Thionium Ion Initiated Medium-Sized Ring Formation: The Total Synthesis of Asteriscunolide D J. Am. Chem. Soc. 2012, 134, 1474-1477 10.1021/ja210986f
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 1474-1477
    • Trost, B.M.1    Burns, A.C.2    Bartlett, M.J.3    Tautz, T.4    Weiss, A.H.5
  • 306
    • 84864417895 scopus 로고    scopus 로고
    • Liquid Chromatographic Separation of Darunavir Enantiomers on Coated and Immobilized Amylose Tris(3, 5-dimethylphenylcarbamate) Chiral Stationary Phases
    • Rao, R. N.; Kumar, K. N.; Naidu, C. G. Liquid Chromatographic Separation of Darunavir Enantiomers on Coated and Immobilized Amylose Tris(3, 5-dimethylphenylcarbamate) Chiral Stationary Phases Chirality 2012, 24, 652-660 10.1002/chir.22060
    • (2012) Chirality , vol.24 , pp. 652-660
    • Rao, R.N.1    Kumar, K.N.2    Naidu, C.G.3
  • 307
    • 54049148506 scopus 로고    scopus 로고
    • Comparative Study of Coated and Immobilized Polysaccharide-based Chiral Stationary Phases and Their Applicability in the Resolution of Enantiomers
    • Thunberg, L.; Hashemi, J.; Andersson, S. Comparative Study of Coated and Immobilized Polysaccharide-based Chiral Stationary Phases and Their Applicability in the Resolution of Enantiomers J. Chromatogr. B: Anal. Technol. Biomed. Life Sci. 2008, 875, 72-80 10.1016/j.jchromb.2008.07.044
    • (2008) J. Chromatogr. B: Anal. Technol. Biomed. Life Sci. , vol.875 , pp. 72-80
    • Thunberg, L.1    Hashemi, J.2    Andersson, S.3
  • 308
    • 84919343752 scopus 로고    scopus 로고
    • Construction of Enantioenriched [3.1.0] Bicycles via a Ruthenium-Catalyzed Asymmetric Redox Bicycloisomerization Reaction
    • Trost, B. M.; Ryan, M. C.; Rao, M.; Markovic, T. Z. Construction of Enantioenriched [3.1.0] Bicycles via a Ruthenium-Catalyzed Asymmetric Redox Bicycloisomerization Reaction J. Am. Chem. Soc. 2014, 136, 17422-17425 10.1021/ja510968h
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 17422-17425
    • Trost, B.M.1    Ryan, M.C.2    Rao, M.3    Markovic, T.Z.4
  • 309
    • 33646543981 scopus 로고    scopus 로고
    • Chiral Separations of Piperidine-2,6-dione Analogues on Chiralpak IA and Chiralpak IB Columns by Using HPLC
    • Ali, I.; Naim, L.; Ghanem, A.; Aboul-Enein, H. Y. Chiral Separations of Piperidine-2,6-dione Analogues on Chiralpak IA and Chiralpak IB Columns by Using HPLC Talanta 2006, 69, 1013-1017 10.1016/j.talanta.2005.12.004
    • (2006) Talanta , vol.69 , pp. 1013-1017
    • Ali, I.1    Naim, L.2    Ghanem, A.3    Aboul-Enein, H.Y.4
  • 310
    • 80455173353 scopus 로고    scopus 로고
    • Unusual Chromatographic Enantioseparation Behavior of Naproxen on an Immobilized Polysaccharide-Based Chiral Stationary Phase
    • Xiang, C.; Liu, G.; Kang, S.; Guo, X.; Yao, B.; Weng, W.; Zeng, Q. Unusual Chromatographic Enantioseparation Behavior of Naproxen on an Immobilized Polysaccharide-Based Chiral Stationary Phase J. Chromatogr. A 2011, 1218, 8718-8721 10.1016/j.chroma.2011.10.014
    • (2011) J. Chromatogr. A , vol.1218 , pp. 8718-8721
    • Xiang, C.1    Liu, G.2    Kang, S.3    Guo, X.4    Yao, B.5    Weng, W.6    Zeng, Q.7
  • 311
    • 79751503924 scopus 로고    scopus 로고
    • Analytical and Semi-Preparative HPLC Enantioseparation of Novel Pyridazin-3(2H)-one Derivatives with α-Aminophosphonate Moiety Using Immobilized Polysaccharide Chiral Stationary Phases
    • Zhang, Y.; Zhang, X.; Zhou, J.; Song, B.; Bhadury, P. S.; Hu, D.; Yang, S. Analytical and Semi-Preparative HPLC Enantioseparation of Novel Pyridazin-3(2H)-one Derivatives with α-Aminophosphonate Moiety Using Immobilized Polysaccharide Chiral Stationary Phases J. Sep. Sci. 2011, 34, 402-408 10.1002/jssc.201000705
    • (2011) J. Sep. Sci. , vol.34 , pp. 402-408
    • Zhang, Y.1    Zhang, X.2    Zhou, J.3    Song, B.4    Bhadury, P.S.5    Hu, D.6    Yang, S.7
  • 312
    • 34249680757 scopus 로고    scopus 로고
    • Exploring Solvent Versatility in Immobilized Cellulose-Based Chiral Stationary Phase for the Enantioselective Liquid Chromatographic Resolution of Racemates
    • Ghanem, A. Exploring Solvent Versatility in Immobilized Cellulose-Based Chiral Stationary Phase for the Enantioselective Liquid Chromatographic Resolution of Racemates J. Sep. Sci. 2007, 30, 1019-1028 10.1002/jssc.200600357
    • (2007) J. Sep. Sci. , vol.30 , pp. 1019-1028
    • Ghanem, A.1
  • 314
    • 84897507841 scopus 로고    scopus 로고
    • Enantioselective Synthesis of Planar Chiral Ferrocenes via Pd(0)-catalyzed Intramolecular Direct C-H Bond Arylation
    • Gao, D.-W.; Yin, Q.; Gu, Q.; You, S.-L. Enantioselective Synthesis of Planar Chiral Ferrocenes via Pd(0)-catalyzed Intramolecular Direct C-H Bond Arylation J. Am. Chem. Soc. 2014, 136, 4841-4844 10.1021/ja500444v
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 4841-4844
    • Gao, D.-W.1    Yin, Q.2    Gu, Q.3    You, S.-L.4
  • 315
    • 84862672181 scopus 로고    scopus 로고
    • Highly Stereoselective Synthesis of α-Alkyl-α-hydroxycarboxylic Acid Derivatives Catalyzed by a Dinuclear Zinc Complex
    • Trost, B. M.; Hirano, K. Highly Stereoselective Synthesis of α-Alkyl-α-hydroxycarboxylic Acid Derivatives Catalyzed by a Dinuclear Zinc Complex Angew. Chem., Int. Ed. 2012, 51, 6480-6483 10.1002/anie.201201116
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 6480-6483
    • Trost, B.M.1    Hirano, K.2
  • 316
    • 84866390866 scopus 로고    scopus 로고
    • Highly Enantioselective Catalytic [6 + 3] Cycloadditions of Azomethine Ylides
    • Potowski, M.; Bauer, J. O.; Strohmann, C.; Antonchick, A. P.; Waldmann, H. Highly Enantioselective Catalytic [6 + 3] Cycloadditions of Azomethine Ylides Angew. Chem., Int. Ed. 2012, 51, 9512-9516 10.1002/anie.201204394
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 9512-9516
    • Potowski, M.1    Bauer, J.O.2    Strohmann, C.3    Antonchick, A.P.4    Waldmann, H.5
  • 317
    • 84862106057 scopus 로고    scopus 로고
    • Asymmetric N-Allylation of Indoles through the Iridium-Catalyzed Allylic Alkylation/Oxidation of Indolines
    • Liu, W.-B.; Zhang, X.; Dai, L.-X.; You, S.-L. Asymmetric N-Allylation of Indoles through the Iridium-Catalyzed Allylic Alkylation/Oxidation of Indolines Angew. Chem., Int. Ed. 2012, 51, 5183-5187 10.1002/anie.201200649
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 5183-5187
    • Liu, W.-B.1    Zhang, X.2    Dai, L.-X.3    You, S.-L.4
  • 318
    • 77950851526 scopus 로고    scopus 로고
    • Determination of Enantiomerization Barriers of Hypericin and Pseudohypericin by Dynamic High-Performance Liquid Chromatography on Immobilized Polysaccharide-type Chiral Stationary Phases and Off-column Racemization Experiments
    • Ciogli, A.; Bicker, W.; Lindner, W. Determination of Enantiomerization Barriers of Hypericin and Pseudohypericin by Dynamic High-Performance Liquid Chromatography on Immobilized Polysaccharide-type Chiral Stationary Phases and Off-column Racemization Experiments Chirality 2010, 22, 463-471 10.1002/chir.20764
    • (2010) Chirality , vol.22 , pp. 463-471
    • Ciogli, A.1    Bicker, W.2    Lindner, W.3
  • 319
    • 84865851339 scopus 로고    scopus 로고
    • Enantioselective H-bond-directing Approach for Trienamine-mediated Reactions in Asymmetric Synthesis
    • Albrecht, L.; Acosta, F. C.; Fraile, A.; Albrecht, A.; Christensen, J.; Jørgensen, K. A. Enantioselective H-bond-directing Approach for Trienamine-mediated Reactions in Asymmetric Synthesis Angew. Chem., Int. Ed. 2012, 51, 9088-9092 10.1002/anie.201204790
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 9088-9092
    • Albrecht, L.1    Acosta, F.C.2    Fraile, A.3    Albrecht, A.4    Christensen, J.5    Jørgensen, K.A.6
  • 320
    • 66649115674 scopus 로고    scopus 로고
    • Direct High-Performance Liquid Chromatography Enantioseparation of Terazosin on an Immobilised Polysaccharide-Based Chiral Stationary Phase under Polar Organic and Reversed-phase Conditions
    • Ferretti, R.; Gallinella, B.; Torre, F. L.; Zanitti, L.; Turchetto, L.; Mosca, A.; Cirilli, R. Direct High-Performance Liquid Chromatography Enantioseparation of Terazosin on an Immobilised Polysaccharide-Based Chiral Stationary Phase Under Polar Organic and Reversed-phase Conditions J. Chromatogr. A 2009, 1216, 5385-5390 10.1016/j.chroma.2009.05.034
    • (2009) J. Chromatogr. A , vol.1216 , pp. 5385-5390
    • Ferretti, R.1    Gallinella, B.2    Torre, F.L.3    Zanitti, L.4    Turchetto, L.5    Mosca, A.6    Cirilli, R.7
  • 321
    • 84863823491 scopus 로고    scopus 로고
    • Diastereodivergent De-epimerization in Catalytic Asymmetric Allylic Alkylation
    • Audisio, D.; Luparia, M.; Oliveira, M. T.; Klütt, D.; Maulide, N. Diastereodivergent De-epimerization in Catalytic Asymmetric Allylic Alkylation Angew. Chem., Int. Ed. 2012, 51, 7314-7317 10.1002/anie.201202853
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 7314-7317
    • Audisio, D.1    Luparia, M.2    Oliveira, M.T.3    Klütt, D.4    Maulide, N.5
  • 322
    • 84867070315 scopus 로고    scopus 로고
    • Organocatalytic Activation of Polycyclic Aromatic Compounds for Asymmetric Diels-alder Reactions
    • Jiang, H.; Rodríguez-Escrich, C.; Johansen, T. K.; Davis, R. L.; Jørgensen, K. A. Organocatalytic Activation of Polycyclic Aromatic Compounds for Asymmetric Diels-alder Reactions Angew. Chem., Int. Ed. 2012, 51, 10271-10274 10.1002/anie.201205836
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 10271-10274
    • Jiang, H.1    Rodríguez-Escrich, C.2    Johansen, T.K.3    Davis, R.L.4    Jørgensen, K.A.5
  • 323
    • 84880507077 scopus 로고    scopus 로고
    • In-depth Characterization of Six Cellulose Tris-(3,5-dimethylphenylcarbamate) Chiral Stationary Phases in Supercritical Fluid Chromatography
    • Khater, S.; Zhang, Y.; West, C. In-depth Characterization of Six Cellulose Tris-(3,5-dimethylphenylcarbamate) Chiral Stationary Phases in Supercritical Fluid Chromatography J. Chromatogr. A 2013, 1303, 83-93 10.1016/j.chroma.2013.06.040
    • (2013) J. Chromatogr. A , vol.1303 , pp. 83-93
    • Khater, S.1    Zhang, Y.2    West, C.3
  • 324
    • 23444461602 scopus 로고    scopus 로고
    • On the Solvent Versatility in Immobilized Amylose Tris(3,5-Dimethylphenylcarbamate) Chiral Stationary Phase in High Performance Liquid Chromatography: Application to the Asymmetric Cyclopropanation of Olefins
    • Ghanem, A.; Aboul-Enein, H. Y. On the Solvent Versatility in Immobilized Amylose Tris(3,5-Dimethylphenylcarbamate) Chiral Stationary Phase in High Performance Liquid Chromatography: Application to the Asymmetric Cyclopropanation of Olefins Anal. Chim. Acta 2005, 548, 26-32 10.1016/j.aca.2005.05.079
    • (2005) Anal. Chim. Acta , vol.548 , pp. 26-32
    • Ghanem, A.1    Aboul-Enein, H.Y.2
  • 325
    • 30144443257 scopus 로고    scopus 로고
    • Application and Comparison of Immobilized and Coated Amylose Tris-(3,5-Dimethylphenylcarbamate) Chiral Stationary Phases for the Enantioselective Separation of β-blockers Enantiomers by Liquid Chromatography
    • Ghanem, A.; Hoenen, H.; Aboul-Enein, H. Y. Application and Comparison of Immobilized and Coated Amylose Tris-(3,5-Dimethylphenylcarbamate) Chiral Stationary Phases for the Enantioselective Separation of β-blockers Enantiomers by Liquid Chromatography Talanta 2006, 68, 602-609 10.1016/j.talanta.2005.04.050
    • (2006) Talanta , vol.68 , pp. 602-609
    • Ghanem, A.1    Hoenen, H.2    Aboul-Enein, H.Y.3
  • 326
    • 77951587369 scopus 로고    scopus 로고
    • Synthesis and Immobilization of Amylose Derivatives Bearing a 4-tert-Butylbenzoate Group at the 2-Position and 3,5-Dichlorophenylcarbamate/3-(Triethoxysilyl)propylcarbamate Groups at 3- and 6-Positions as Chiral Packing Material for HPLC
    • Shen, J.; Ikai, T.; Shen, X.; Okamoto, Y. Synthesis and Immobilization of Amylose Derivatives Bearing a 4-tert-Butylbenzoate Group at the 2-Position and 3,5-Dichlorophenylcarbamate/3-(Triethoxysilyl)propylcarbamate Groups at 3- and 6-Positions as Chiral Packing Material for HPLC Chem. Lett. 2010, 39, 442-444 10.1246/cl.2010.442
    • (2010) Chem. Lett. , vol.39 , pp. 442-444
    • Shen, J.1    Ikai, T.2    Shen, X.3    Okamoto, Y.4
  • 327
    • 80053924410 scopus 로고    scopus 로고
    • Immobilization and Chromatographic Evaluation of Novel Regioselectively Substituted Amylose-Based Chiral Packing Materials for HPLC
    • Shen, J.; Li, P.; Liu, S.; Shen, X.; Okamoto, Y. Immobilization and Chromatographic Evaluation of Novel Regioselectively Substituted Amylose-Based Chiral Packing Materials for HPLC Chirality 2011, 23, 878-886 10.1002/chir.21000
    • (2011) Chirality , vol.23 , pp. 878-886
    • Shen, J.1    Li, P.2    Liu, S.3    Shen, X.4    Okamoto, Y.5
  • 328
    • 54849406797 scopus 로고    scopus 로고
    • Organic-Inorganic Hybrid Materials for Efficient Enantioseparation Using Cellulose 3,5-Dimethylphenylcarbamate and Tetraethyl Orthosilicate
    • Ikai, T.; Yamamoto, C.; Kamigaito, M.; Okamoto, Y. Organic-Inorganic Hybrid Materials for Efficient Enantioseparation Using Cellulose 3,5-Dimethylphenylcarbamate and Tetraethyl Orthosilicate Chem.-Asian J. 2008, 3, 1494-1499 10.1002/asia.200800022
    • (2008) Chem. - Asian J. , vol.3 , pp. 1494-1499
    • Ikai, T.1    Yamamoto, C.2    Kamigaito, M.3    Okamoto, Y.4
  • 329
    • 0028947992 scopus 로고
    • Computational Studies on Chiral Discrimination Mechanism of Cellulose Trisphenylcarbamate
    • Yashima, E.; Yamada, M.; Kaida, Y.; Okamoto, Y. Computational Studies on Chiral Discrimination Mechanism of Cellulose Trisphenylcarbamate J. Chromatogr. A 1995, 694, 347-354 10.1016/0021-9673(94)01039-H
    • (1995) J. Chromatogr. A , vol.694 , pp. 347-354
    • Yashima, E.1    Yamada, M.2    Kaida, Y.3    Okamoto, Y.4
  • 330
    • 0029949417 scopus 로고    scopus 로고
    • NMR Studies of Chiral Discrimination Relevant to the Liquid Chromatographic Enantioseparation by a Cellulose Phenylcarbamate Derivative
    • Yashima, E.; Yamamoto, C.; Okamoto, Y. NMR Studies of Chiral Discrimination Relevant to the Liquid Chromatographic Enantioseparation by a Cellulose Phenylcarbamate Derivative J. Am. Chem. Soc. 1996, 118, 4036-4048 10.1021/ja960050x
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4036-4048
    • Yashima, E.1    Yamamoto, C.2    Okamoto, Y.3
  • 331
    • 0001854516 scopus 로고
    • An NMR Study of Chiral Recognition Relevant to the Liquid Chromatographic Separation of Enantiomers by a Cellulose Derivative
    • Yashima, E.; Yamada, M.; Okamoto, Y. An NMR Study of Chiral Recognition Relevant to the Liquid Chromatographic Separation of Enantiomers by a Cellulose Derivative Chem. Lett. 1994, 23, 579-582 10.1246/cl.1994.579
    • (1994) Chem. Lett. , vol.23 , pp. 579-582
    • Yashima, E.1    Yamada, M.2    Okamoto, Y.3
  • 332
    • 0030878392 scopus 로고    scopus 로고
    • Chromatographic Enantioseparation and Chiral Discrimination in NMR by Trisphenylcarbamate Derivatives of Cellulose, Amylose, Oligosaccharides, and Cyclodextrins
    • Yashima, E.; Yamada, M.; Yamamoto, C.; Nakashima, M.; Okamoto, Y. Chromatographic Enantioseparation and Chiral Discrimination in NMR by Trisphenylcarbamate Derivatives of Cellulose, Amylose, Oligosaccharides, and Cyclodextrins Enantiomer 1997, 2, 225-240
    • (1997) Enantiomer , vol.2 , pp. 225-240
    • Yashima, E.1    Yamada, M.2    Yamamoto, C.3    Nakashima, M.4    Okamoto, Y.5
  • 333
    • 0031534390 scopus 로고    scopus 로고
    • NMR Studies of Chiral Discrimination by Phenylcarbamate Derivatives of Cellulose
    • Okamoto, Y.; Yashima, E.; Yamamoto, C. NMR Studies of Chiral Discrimination by Phenylcarbamate Derivatives of Cellulose Macromol. Symp. 1997, 120, 127-137 10.1002/masy.19971200114
    • (1997) Macromol. Symp. , vol.120 , pp. 127-137
    • Okamoto, Y.1    Yashima, E.2    Yamamoto, C.3
  • 334
    • 0037164072 scopus 로고    scopus 로고
    • Structural Analysis of Amylose Tris(3,5-dimethylphenylcarbamate) by NMR Relevant to its Chiral Recognition Mechanism in HPLC
    • Yamamoto, C.; Yashima, E.; Okamoto, Y. Structural Analysis of Amylose Tris(3,5-dimethylphenylcarbamate) by NMR Relevant to its Chiral Recognition Mechanism in HPLC J. Am. Chem. Soc. 2002, 124, 12583-12589 10.1021/ja020828g
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 12583-12589
    • Yamamoto, C.1    Yashima, E.2    Okamoto, Y.3
  • 337
    • 0035449458 scopus 로고    scopus 로고
    • Solid-state NMR Characterization of Amylose Tris(3,5-dimethylphenylcarbamate) Chiral Stationary-phase Structure as a Function of Mobile-phase Composition
    • Wenslow, R. M.; Wang, T. Solid-state NMR Characterization of Amylose Tris(3,5-dimethylphenylcarbamate) Chiral Stationary-phase Structure as a Function of Mobile-phase Composition Anal. Chem. 2001, 73, 4190-4195 10.1021/ac0103672
    • (2001) Anal. Chem. , vol.73 , pp. 4190-4195
    • Wenslow, R.M.1    Wang, T.2
  • 338
    • 0027967911 scopus 로고
    • 1H NMR Support for a Proposed Chiral Recognition Model
    • 1H NMR Support for a Proposed Chiral Recognition Model J. Chromatogr. A 1994, 683, 347-353 10.1016/0021-9673(94)00477-3
    • (1994) J. Chromatogr. A , vol.683 , pp. 347-353
    • Pirkle, W.H.1    Welch, C.J.2
  • 339
    • 0022498516 scopus 로고
    • Separation of Drug Stereoisomers by the Formation of β-cyclodextrin Inclusion Complexes
    • Armstrong, D. W.; Ward, T. J.; Armstrong, R. D.; Beesley, T. E. Separation of Drug Stereoisomers by the Formation of β-cyclodextrin Inclusion Complexes Science 1986, 232, 1132-1135 10.1126/science.3704640
    • (1986) Science , vol.232 , pp. 1132-1135
    • Armstrong, D.W.1    Ward, T.J.2    Armstrong, R.D.3    Beesley, T.E.4
  • 341
    • 0028901707 scopus 로고
    • Theoretical Studies of Type II-V Chiral Stationary Phases
    • Lipkowitz, K. B. Theoretical Studies of Type II-V Chiral Stationary Phases J. Chromatogr. A 1995, 694, 15-37 10.1016/0021-9673(94)00956-A
    • (1995) J. Chromatogr. A , vol.694 , pp. 15-37
    • Lipkowitz, K.B.1
  • 342
    • 0035847244 scopus 로고    scopus 로고
    • Atomistic Modeling of Enantioselection in Chromatography
    • Lipkowitz, K. B. Atomistic Modeling of Enantioselection in Chromatography J. Chromatogr. A 2001, 906, 417-442 10.1016/S0021-9673(00)00946-8
    • (2001) J. Chromatogr. A , vol.906 , pp. 417-442
    • Lipkowitz, K.B.1
  • 343
    • 39749191319 scopus 로고    scopus 로고
    • Molecular Dynamic Theories in Chromatography
    • Felinger, A. Molecular Dynamic Theories in Chromatography J. Chromatogr. A 2008, 1184, 20-41 10.1016/j.chroma.2007.12.066
    • (2008) J. Chromatogr. A , vol.1184 , pp. 20-41
    • Felinger, A.1
  • 344
    • 41849147190 scopus 로고    scopus 로고
    • Molecular Dynamics Study of Chiral Recognition for the Whelk-01 Chiral Stationary Phase
    • Zhao, C. F.; Cann, N. M. Molecular Dynamics Study of Chiral Recognition for the Whelk-01 Chiral Stationary Phase Anal. Chem. 2008, 80, 2426-2438 10.1021/ac702126y
    • (2008) Anal. Chem. , vol.80 , pp. 2426-2438
    • Zhao, C.F.1    Cann, N.M.2
  • 345
    • 0025678085 scopus 로고
    • Optical Resolving Ability of 3,5-Dimethylphenylcarbamates of Oligosaccarides and Cyclodextrins
    • Aburatani, R.; Okamoto, Y.; Hatada, K. Optical Resolving Ability of 3,5-Dimethylphenylcarbamates of Oligosaccarides and Cyclodextrins Bull. Chem. Soc. Jpn. 1990, 63, 3606-3610 10.1246/bcsj.63.3606
    • (1990) Bull. Chem. Soc. Jpn. , vol.63 , pp. 3606-3610
    • Aburatani, R.1    Okamoto, Y.2    Hatada, K.3
  • 346
    • 0023422367 scopus 로고
    • Solution Properties and Chain Conformation Characteristics of Cellulose Tricarbanilate
    • Danhelka, J.; Netopilik, M.; Bohdanecky, M. Solution Properties and Chain Conformation Characteristics of Cellulose Tricarbanilate J. Polym. Sci., Part B: Polym. Phys. 1987, 25, 1801-1815 10.1002/polb.1987.090250902
    • (1987) J. Polym. Sci., Part B: Polym. Phys. , vol.25 , pp. 1801-1815
    • Danhelka, J.1    Netopilik, M.2    Bohdanecky, M.3
  • 347
    • 0036249964 scopus 로고    scopus 로고
    • Chromatographic Enantioseparation by Cycloalkylcarbamate Derivatives of Cellulose and Amylose
    • Kubota, T.; Yamamoto, C.; Okamoto, Y. Chromatographic Enantioseparation by Cycloalkylcarbamate Derivatives of Cellulose and Amylose Chirality 2002, 14, 372-376 10.1002/chir.10095
    • (2002) Chirality , vol.14 , pp. 372-376
    • Kubota, T.1    Yamamoto, C.2    Okamoto, Y.3
  • 348
    • 34249887364 scopus 로고    scopus 로고
    • Effects of Backbone and Side Chain on the Molecular Environments of Chiral Cavities in Polysaccharide-Based Biopolymers
    • Kasat, R. B.; Wang, N. H. L.; Franses, E. I. Effects of Backbone and Side Chain on the Molecular Environments of Chiral Cavities in Polysaccharide-Based Biopolymers Biomacromolecules 2007, 8, 1676-1685 10.1021/bm070006h
    • (2007) Biomacromolecules , vol.8 , pp. 1676-1685
    • Kasat, R.B.1    Wang, N.H.L.2    Franses, E.I.3
  • 349
    • 42149186311 scopus 로고    scopus 로고
    • Experimental Probing and Modeling of Key Sorbent-Solute Interaction of Norephedorine Enantiomers with Polysaccharide-Based Chiral Stationary Phases
    • Kasat, R. B.; Wang, N.-H. L.; Franses, E. I. Experimental Probing and Modeling of Key Sorbent-Solute Interaction of Norephedorine Enantiomers with Polysaccharide-Based Chiral Stationary Phases J. Chromatogr. 2008, 1190, 110-119 10.1016/j.chroma.2008.02.116
    • (2008) J. Chromatogr. , vol.1190 , pp. 110-119
    • Kasat, R.B.1    Wang, N.-H.L.2    Franses, E.I.3
  • 350
    • 53649085863 scopus 로고    scopus 로고
    • Vibrational Circular Dichroism of Amylose Carbamate: Structure and Solvent-Induced Conformational Changes
    • Ma, S. L.; Shen, S.; Lee, H.; Yee, N.; Senanayake, C.; Nafie, L. A.; Grinberg, N. Vibrational Circular Dichroism of Amylose Carbamate: Structure and Solvent-Induced Conformational Changes Tetrahedron: Asymmetry 2008, 19, 2111-2114 10.1016/j.tetasy.2008.08.027
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 2111-2114
    • Ma, S.L.1    Shen, S.2    Lee, H.3    Yee, N.4    Senanayake, C.5    Nafie, L.A.6    Grinberg, N.7
  • 351
    • 0032099972 scopus 로고    scopus 로고
    • Enantioseparation on 3,5-Dichloro- and 3,5-Dimethylphenylcarbamates of Polysaccharides as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Okamoto, Y.; Noguchi, J.; Yashima, E. Enantioseparation on 3,5-Dichloro- and 3,5-Dimethylphenylcarbamates of Polysaccharides as Chiral Stationary Phases for High-Performance Liquid Chromatography React. Funct. Polym. 1998, 37, 183-188 10.1016/S1381-5148(97)00135-1
    • (1998) React. Funct. Polym. , vol.37 , pp. 183-188
    • Okamoto, Y.1    Noguchi, J.2    Yashima, E.3
  • 352
    • 35948996970 scopus 로고    scopus 로고
    • Synthesis and Characterization of the Chiral Stationary Phase Based on Chitosan
    • Son, S. H.; Jegal, J. Synthesis and Characterization of the Chiral Stationary Phase Based on Chitosan J. Appl. Polym. Sci. 2007, 106, 2989-2996 10.1002/app.26908
    • (2007) J. Appl. Polym. Sci. , vol.106 , pp. 2989-2996
    • Son, S.H.1    Jegal, J.2
  • 353
    • 1842864082 scopus 로고    scopus 로고
    • Chiral Recognition Ability of Curdlan Triacetate: Solvent and Temperature Effects
    • Toga, Y.; Ichida, A.; Shibata, T. Chiral Recognition Ability of Curdlan Triacetate: Solvent and Temperature Effects Chirality 2004, 16, 272-276 10.1002/chir.20020
    • (2004) Chirality , vol.16 , pp. 272-276
    • Toga, Y.1    Ichida, A.2    Shibata, T.3
  • 354
    • 0013370943 scopus 로고    scopus 로고
    • Preparation of a β-Cyclodextrin-modified N-Carboxymethylchitosan and its Chromatographic Behavior as a Chiral HPLC Stationary Phase
    • Kurauchi, Y.; Ono, H.; Wang, B.; Egashira, N.; Ohga, K. Preparation of a β-Cyclodextrin-modified N-Carboxymethylchitosan and its Chromatographic Behavior as a Chiral HPLC Stationary Phase Anal. Sci. 1997, 13, 47-52 10.2116/analsci.13.47
    • (1997) Anal. Sci. , vol.13 , pp. 47-52
    • Kurauchi, Y.1    Ono, H.2    Wang, B.3    Egashira, N.4    Ohga, K.5
  • 355
    • 0029986294 scopus 로고    scopus 로고
    • Chiral Discrimination by HPLC on Aryl Carbamate Derivatives of Chitin Coated onto Microporous Aminopropyl Silica
    • Cass, Q. B.; Bassi, A. L.; Matlin, S. A. Chiral Discrimination by HPLC on Aryl Carbamate Derivatives of Chitin Coated onto Microporous Aminopropyl Silica Chirality 1996, 8, 131-135 10.1002/(SICI)1520-636X(1996)8:1131::AID-CHIR193.0.CO;2-O
    • (1996) Chirality , vol.8 , pp. 131-135
    • Cass, Q.B.1    Bassi, A.L.2    Matlin, S.A.3
  • 356
    • 10744228647 scopus 로고    scopus 로고
    • High-Performance Liquid Chromatographic Enantioseparation Using Chitin Carbamate Derivatives as Chiral Stationary Phases
    • Yamamoto, C.; Hayashi, T.; Okamoto, Y. High-Performance Liquid Chromatographic Enantioseparation Using Chitin Carbamate Derivatives as Chiral Stationary Phases J. Chromatogr. A 2003, 1021, 83-91 10.1016/j.chroma.2003.09.017
    • (2003) J. Chromatogr. A , vol.1021 , pp. 83-91
    • Yamamoto, C.1    Hayashi, T.2    Okamoto, Y.3
  • 357
    • 39749198490 scopus 로고    scopus 로고
    • Enantioseparation Using Urea and Imide Bearing Chitosan Phenylcarbamate Derivatives as Chiral Stationary Phases for High-Performance Liquid Chromatography
    • Yamamoto, C.; Fujisawa, M.; Kamigaito, M.; Okamoto, Y. Enantioseparation Using Urea and Imide Bearing Chitosan Phenylcarbamate Derivatives as Chiral Stationary Phases for High-Performance Liquid Chromatography Chirality 2008, 20, 288-294 10.1002/chir.20430
    • (2008) Chirality , vol.20 , pp. 288-294
    • Yamamoto, C.1    Fujisawa, M.2    Kamigaito, M.3    Okamoto, Y.4
  • 358
    • 84891761709 scopus 로고    scopus 로고
    • Synthesis and Chiral Recognition Ability of Chitosan Derivatives with Different 4-Chlorophenylcarbamate-Urea Structures
    • Zhang, L.; Shen, J.; Zuo, W.; Okamoto, Y. Synthesis and Chiral Recognition Ability of Chitosan Derivatives with Different 4-Chlorophenylcarbamate-Urea Structures Chem. Lett. 2014, 43, 92-94 10.1246/cl.130834
    • (2014) Chem. Lett. , vol.43 , pp. 92-94
    • Zhang, L.1    Shen, J.2    Zuo, W.3    Okamoto, Y.4
  • 359
    • 77950166513 scopus 로고    scopus 로고
    • Synthesis and Structural Characterization of Phenylcarbamate Derivatives of Chitin and Chitosan
    • Matsubara, T.; Miyashita, Y.; Nishio, Y. Synthesis and Structural Characterization of Phenylcarbamate Derivatives of Chitin and Chitosan Kobunshi Ronbunshu 2010, 67, 135-142 10.1295/koron.67.135
    • (2010) Kobunshi Ronbunshu , vol.67 , pp. 135-142
    • Matsubara, T.1    Miyashita, Y.2    Nishio, Y.3
  • 360
    • 58549096731 scopus 로고    scopus 로고
    • Molecular Structure and Liquid-Crystalline Characteristics of Chitosan Phenylcarbamate
    • Kuse, Y.; Asahina, D.; Nishio, Y. Molecular Structure and Liquid-Crystalline Characteristics of Chitosan Phenylcarbamate Biomacromolecules 2009, 10, 166-173 10.1021/bm801073e
    • (2009) Biomacromolecules , vol.10 , pp. 166-173
    • Kuse, Y.1    Asahina, D.2    Nishio, Y.3
  • 361
    • 84908070261 scopus 로고    scopus 로고
    • Synthesis of Chitosan 3,5-Dimethylphenyl-2-urea Derivatives and Their Applications as Chiral Stationary Phases for HPLC
    • Zhang, L.; Shen, J.; Zuo, W.; Okamoto, Y. Synthesis of Chitosan 3,5-Dimethylphenyl-2-urea Derivatives and Their Applications as Chiral Stationary Phases for HPLC J. Chromatogr. A 2014, 1365, 86-93 10.1016/j.chroma.2014.09.002
    • (2014) J. Chromatogr. A , vol.1365 , pp. 86-93
    • Zhang, L.1    Shen, J.2    Zuo, W.3    Okamoto, Y.4
  • 362
    • 84937812682 scopus 로고    scopus 로고
    • Synthesis and Enantioseparation Ability of Xylan Bisphenylcarbamate Derivatives as Chiral Stationary Phases in HPLC
    • Li, G.; Shen, J.; Li, Q.; Okamoto, Y. Synthesis and Enantioseparation Ability of Xylan Bisphenylcarbamate Derivatives as Chiral Stationary Phases in HPLC Chirality 2015, 27, 518 10.1002/chir.22472
    • (2015) Chirality , vol.27 , pp. 518
    • Li, G.1    Shen, J.2    Li, Q.3    Okamoto, Y.4
  • 363
    • 0026065599 scopus 로고
    • Effect of the Configuration of the Substituents of Derivatized β-Cyclodextrin Bonded Phases on Enantioselectivity in Normal-Phase Liquid Chromatography
    • Stalcup, A. M.; Chang, S. C.; Armstrong, D. W. Effect of the Configuration of the Substituents of Derivatized β-Cyclodextrin Bonded Phases on Enantioselectivity in Normal-Phase Liquid Chromatography J. Chromatogr. 1991, 540, 113-128 10.1016/S0021-9673(01)88802-6
    • (1991) J. Chromatogr. , vol.540 , pp. 113-128
    • Stalcup, A.M.1    Chang, S.C.2    Armstrong, D.W.3
  • 364
    • 0022011425 scopus 로고
    • Separation of Metalloenen Enantiomers by Liquid Chromatography: Chiral Recognition via Cyclodextrin Bonded Phases
    • Armstrong, D. W.; DeMond, W.; Czech, B. P. Separation of Metalloenen Enantiomers by Liquid Chromatography: Chiral Recognition via Cyclodextrin Bonded Phases Anal. Chem. 1985, 57, 481-484 10.1021/ac50001a037
    • (1985) Anal. Chem. , vol.57 , pp. 481-484
    • Armstrong, D.W.1    Demond, W.2    Czech, B.P.3
  • 365
    • 33745369922 scopus 로고    scopus 로고
    • Separation of Enantiomers of β-Lactams by HPLC Using Cyclodextrin-Based Chiral Stationary Phases
    • Sun, P.; Wang, C.; Armstrong, D. W.; Peter, A.; Forro, E. Separation of Enantiomers of β-Lactams by HPLC Using Cyclodextrin-Based Chiral Stationary Phases J. Liq. Chromatogr. Relat. Technol. 2006, 29, 1847-1860 10.1080/10826070600757540
    • (2006) J. Liq. Chromatogr. Relat. Technol. , vol.29 , pp. 1847-1860
    • Sun, P.1    Wang, C.2    Armstrong, D.W.3    Peter, A.4    Forro, E.5
  • 366
    • 0026060808 scopus 로고
    • (R)- and (S)-Naphthylethylcarbamate Substituted β-Cyclodextrin Bonded Stationary Phases for the Reversed-Phase Liquid Chromatographic Separation of Enantiomers
    • Armstrong, D. W.; Chang, C. D.; Lee, S. H. (R)- and (S)-Naphthylethylcarbamate Substituted β-Cyclodextrin Bonded Stationary Phases for the Reversed-Phase Liquid Chromatographic Separation of Enantiomers J. Chromatogr. 1991, 539, 83-90 10.1016/S0021-9673(01)95362-2
    • (1991) J. Chromatogr. , vol.539 , pp. 83-90
    • Armstrong, D.W.1    Chang, C.D.2    Lee, S.H.3
  • 367
    • 77954176885 scopus 로고    scopus 로고
    • Effective Enantiomeric Separations of Racemic Primary Amines by the Isopropyl Carbamate-Cyclofructan6 Chiral Stationary Phase
    • Sun, P.; Armstrong, D. W. Effective Enantiomeric Separations of Racemic Primary Amines by the Isopropyl Carbamate-Cyclofructan6 Chiral Stationary Phase J. Chromatogr. A 2010, 1217, 4904-4918 10.1016/j.chroma.2010.04.079
    • (2010) J. Chromatogr. A , vol.1217 , pp. 4904-4918
    • Sun, P.1    Armstrong, D.W.2
  • 369
    • 79951516336 scopus 로고    scopus 로고
    • Characterization of New R-Naphthylethyl Cyclofructan 6 Chiral Stationary Phase and Its Comparison with R-Naphthylethyl Beta-Cyclodextrin-Based Column
    • Kalikova, K.; Janeckova, L.; Armstrong, D. W.; Tesarova, E. Characterization of New R-Naphthylethyl Cyclofructan 6 Chiral Stationary Phase and Its Comparison with R-Naphthylethyl Beta-Cyclodextrin-Based Column J. Chromatogr. A 2011, 1218, 1393-1398 10.1016/j.chroma.2011.01.023
    • (2011) J. Chromatogr. A , vol.1218 , pp. 1393-1398
    • Kalikova, K.1    Janeckova, L.2    Armstrong, D.W.3    Tesarova, E.4
  • 370
    • 84860189208 scopus 로고    scopus 로고
    • High-Performance Liquid Chromatographic Enantioseparation of Amino Compounds on Newly Developed Cyclofructan-Based Chiral Stationary Phases
    • Aranyi, A.; Bagi, A.; Ilisz, I.; Pataj, Z.; Fulop, F.; Armstrong, D. W.; Antal, P. High-Performance Liquid Chromatographic Enantioseparation of Amino Compounds on Newly Developed Cyclofructan-Based Chiral Stationary Phases J. Sep. Sci. 2012, 35, 617-624 10.1002/jssc.201100921
    • (2012) J. Sep. Sci. , vol.35 , pp. 617-624
    • Aranyi, A.1    Bagi, A.2    Ilisz, I.3    Pataj, Z.4    Fulop, F.5    Armstrong, D.W.6    Antal, P.7
  • 371
    • 84868091794 scopus 로고    scopus 로고
    • Chiral HPLC Separation on Derivatized Cyclofructan versus Cyclodextrin Stationary Phases
    • Vozka, J.; Kalikova, K.; Janeckova, L.; Armstrong, D. W.; Tesarova, E. Chiral HPLC Separation on Derivatized Cyclofructan versus Cyclodextrin Stationary Phases Anal. Lett. 2012, 45, 2344-2358 10.1080/00032719.2012.686128
    • (2012) Anal. Lett. , vol.45 , pp. 2344-2358
    • Vozka, J.1    Kalikova, K.2    Janeckova, L.3    Armstrong, D.W.4    Tesarova, E.5
  • 372
    • 84871928356 scopus 로고    scopus 로고
    • Stereoselective Separation of Spironindoline Phytoalexins on R-Naphthylethyl Cyclofructan 6-Based Chiral Stationary Phase
    • Gondova, T.; Petrovaj, J.; Kutschy, P.; Armstrong, D. W. Stereoselective Separation of Spironindoline Phytoalexins on R-Naphthylethyl Cyclofructan 6-Based Chiral Stationary Phase J. Chromatogr. A 2013, 1272, 100-105 10.1016/j.chroma.2012.11.083
    • (2013) J. Chromatogr. A , vol.1272 , pp. 100-105
    • Gondova, T.1    Petrovaj, J.2    Kutschy, P.3    Armstrong, D.W.4
  • 374
    • 0020965261 scopus 로고
    • Direct Liquid Chromatographic Separation of Enantiomers on Immobilized Protein Stationary Phases. III. Optical Resolution of a Series of N-Aroyl d,l-Amino Acids by High-Performance Liquid Chromatography on Bovine Serum Albumin Covalently Bound to Silica
    • Allenmark, S.; Bomgren, B.; Boren, H. Direct Liquid Chromatographic Separation of Enantiomers on Immobilized Protein Stationary Phases. III. Optical Resolution of a Series of N-Aroyl d,l-Amino Acids by High-Performance Liquid Chromatography on Bovine Serum Albumin Covalently Bound to Silica J. Chromatogr. 1983, 264, 63-68 10.1016/S0021-9673(01)95006-X
    • (1983) J. Chromatogr. , vol.264 , pp. 63-68
    • Allenmark, S.1    Bomgren, B.2    Boren, H.3
  • 375
    • 9944250646 scopus 로고
    • Synthesis and Chromatographic Properties of an HPLC Chiral Stationary Phase Based upon Human Serum Albumin
    • Domenici, E.; Bertucci, C.; Salvadori, P.; Felix, G.; Cahagne, I.; Montellier, S.; Wainer, I. W. Synthesis and Chromatographic Properties of an HPLC Chiral Stationary Phase Based upon Human Serum Albumin Chromatographia 1990, 29, 170-176 10.1007/BF02268706
    • (1990) Chromatographia , vol.29 , pp. 170-176
    • Domenici, E.1    Bertucci, C.2    Salvadori, P.3    Felix, G.4    Cahagne, I.5    Montellier, S.6    Wainer, I.W.7
  • 376
    • 0021090901 scopus 로고
    • 1-Acid Glycoprotein as the Chiral Stationary Phase
    • 1-Acid Glycoprotein as the Chiral Stationary Phase J. Chromatogr. A 1983, 269, 71-80 10.1016/S0021-9673(01)90787-3
    • (1983) J. Chromatogr. A , vol.269 , pp. 71-80
    • Hermansson, J.1
  • 377
    • 85008137136 scopus 로고
    • Direct Liquid-Chromatographic Resolution of Racemic Compounds. Use of Ovomucoid as a Column Ligand
    • Miwa, T.; Ichikawa, M.; Tsuno, M.; Hattori, T.; Miyakawa, T.; Kayano, M.; Miyake, Y. Direct Liquid-Chromatographic Resolution of Racemic Compounds. Use of Ovomucoid as a Column Ligand Chem. Pharm. Bull. 1987, 35, 682-686 10.1248/cpb.35.682
    • (1987) Chem. Pharm. Bull. , vol.35 , pp. 682-686
    • Miwa, T.1    Ichikawa, M.2    Tsuno, M.3    Hattori, T.4    Miyakawa, T.5    Kayano, M.6    Miyake, Y.7
  • 378
    • 0000421827 scopus 로고
    • Characteristics of an Avidin-Conjugated Column in Direct Liquid Chromatographic Resolution of Racemic Compounds
    • Miwa, T.; Miyakawa, T.; Miyake, Y. Characteristics of an Avidin-Conjugated Column in Direct Liquid Chromatographic Resolution of Racemic Compounds J. Chromatogr. A 1988, 457, 227-233 10.1016/S0021-9673(01)82070-7
    • (1988) J. Chromatogr. A , vol.457 , pp. 227-233
    • Miwa, T.1    Miyakawa, T.2    Miyake, Y.3
  • 379
    • 0000799144 scopus 로고
    • Immobilized Cellulase (CBH I) as a Chiral Stationary Phase for Direct Resolution of Enantiomers
    • Erlandsson, P.; Marle, I.; Hansson, L.; Isaksson, R.; Pettersson, C.; Pettersson, G. Immobilized Cellulase (CBH I) as a Chiral Stationary Phase for Direct Resolution of Enantiomers J. Am. Chem. Soc. 1990, 112, 4573-4574 10.1021/ja00167a081
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 4573-4574
    • Erlandsson, P.1    Marle, I.2    Hansson, L.3    Isaksson, R.4    Pettersson, C.5    Pettersson, G.6
  • 381
    • 0026595584 scopus 로고
    • Retention and Enantioselectivity of Racemic Solutes on a Modified Ovomucoid-Bonded Column. I. Cross-linking with Glutaraldehyde
    • Haginaka, J.; Seyama, C.; Yasuda, H.; Fujima, H.; Wada, H. Retention and Enantioselectivity of Racemic Solutes on a Modified Ovomucoid-Bonded Column. I. Cross-linking with Glutaraldehyde J. Chromatogr. A 1992, 592, 301-308 10.1016/0021-9673(92)85100-8
    • (1992) J. Chromatogr. A , vol.592 , pp. 301-308
    • Haginaka, J.1    Seyama, C.2    Yasuda, H.3    Fujima, H.4    Wada, H.5
  • 382
    • 0024415562 scopus 로고
    • Use of a Fragment of Bovine Serum Albumin as a Chiral Stationary Phase in Liquid Chromatography
    • Erlandsson, P.; Nilsson, S. Use of a Fragment of Bovine Serum Albumin as a Chiral Stationary Phase in Liquid Chromatography J. Chromatogr. A 1989, 482, 35-51 10.1016/S0021-9673(01)93205-4
    • (1989) J. Chromatogr. A , vol.482 , pp. 35-51
    • Erlandsson, P.1    Nilsson, S.2
  • 383
    • 0027488944 scopus 로고
    • Chiral Stationary Phases Based on Intact and Fragmented Cellobiohydrolase I Immobilized on Silica
    • Marle, I.; Jönsson, S.; Isaksson, R.; Pettersson, C.; Pettersson, G. Chiral Stationary Phases Based on Intact and Fragmented Cellobiohydrolase I Immobilized on Silica J. Chromatogr. A 1993, 648, 333-347 10.1016/0021-9673(93)80415-5
    • (1993) J. Chromatogr. A , vol.648 , pp. 333-347
    • Marle, I.1    Jönsson, S.2    Isaksson, R.3    Pettersson, C.4    Pettersson, G.5
  • 385
    • 0024302176 scopus 로고
    • Main-Chain Chirality and Optical Activity in Polymers Consisting of C-C Chains
    • Wulff, G. Main-Chain Chirality and Optical Activity in Polymers Consisting of C-C Chains Angew. Chem., Int. Ed. Engl. 1989, 28, 21-37 10.1002/anie.198900211
    • (1989) Angew. Chem., Int. Ed. Engl. , vol.28 , pp. 21-37
    • Wulff, G.1
  • 386
    • 0028873867 scopus 로고
    • Molecular Imprinting in Cross-Linked Materials with the Aid of Molecular Templates - A Way towards Artificial Antibodies
    • Wulff, G. Molecular Imprinting in Cross-Linked Materials with the Aid of Molecular Templates-A Way towards Artificial Antibodies Angew. Chem., Int. Ed. Engl. 1995, 34, 1812-1832 10.1002/anie.199518121
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1812-1832
    • Wulff, G.1
  • 387
    • 84888012462 scopus 로고    scopus 로고
    • Fourty Years of Molecular Imprinting in Synthetic Polymers: Origin, Features and Perspectives
    • Wulff, G. Fourty Years of Molecular Imprinting in Synthetic Polymers: Origin, Features and Perspectives Microchim. Acta 2013, 180, 1359-1370 10.1007/s00604-013-0992-9
    • (2013) Microchim. Acta , vol.180 , pp. 1359-1370
    • Wulff, G.1
  • 388
    • 0033118269 scopus 로고    scopus 로고
    • MIPs as Chromatographic Stationary
    • Remcho, V. T.; Tam, Z. J. MIPs as Chromatographic Stationary Anal. Chem. 1999, 71, 248A-255A 10.1021/ac990292q
    • (1999) Anal. Chem. , vol.71 , pp. 248A-255A
    • Remcho, V.T.1    Tam, Z.J.2
  • 389
    • 0001186422 scopus 로고    scopus 로고
    • Molecular Imprinting-Based Biomimetic Sensors Could Provide an Alternative to often Unstable Biosensors for Industry, Medicine, and Environmental Analysis
    • Kriz, D.; Ramstrom, O.; Mosbach, K. Molecular Imprinting-Based Biomimetic Sensors Could Provide an Alternative to often Unstable Biosensors for Industry, Medicine, and Environmental Analysis Anal. Chem. 1997, 69, 345A-349A 10.1021/ac971657e
    • (1997) Anal. Chem. , vol.69 , pp. 345A-349A
    • Kriz, D.1    Ramstrom, O.2    Mosbach, K.3
  • 390
    • 0000239068 scopus 로고
    • Chirality of Vinyl Polymers. the Preparation of Chiral Cavities in Synthetic Polymers
    • Wulff, G.; Kemmer, R.; Vietmeier, J.; Poll, H. G. Chirality of Vinyl Polymers. The Preparation of Chiral Cavities in Synthetic Polymers Nouv. J. Chim. 1982, 6, 681-687
    • (1982) Nouv. J. Chim. , vol.6 , pp. 681-687
    • Wulff, G.1    Kemmer, R.2    Vietmeier, J.3    Poll, H.G.4
  • 391
    • 0024055613 scopus 로고
    • Highly Enantioselective and Substrate-selective Polymers Obtained by Molecular Imprinting Utilizing Noncovalent Interactions. NMR and Chromatographic Studies on the Nature of Recognition
    • Sellergren, B.; Lepistö, M.; Mosbach, K. Highly Enantioselective and Substrate-selective Polymers Obtained by Molecular Imprinting Utilizing Noncovalent Interactions. NMR and Chromatographic Studies on the Nature of Recognition J. Am. Chem. Soc. 1988, 110, 5853-5860 10.1021/ja00225a041
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5853-5860
    • Sellergren, B.1    Lepistö, M.2    Mosbach, K.3
  • 392
    • 0027447855 scopus 로고
    • Drug Assay Using Antibody Mimics Made by Molecular Imprinting
    • Vlatakis, G.; Andersson, L. I.; Müller, R.; Mosbach, K. Drug Assay Using Antibody Mimics Made by Molecular Imprinting Nature 1993, 361, 645-647 10.1038/361645a0
    • (1993) Nature , vol.361 , pp. 645-647
    • Vlatakis, G.1    Andersson, L.I.2    Müller, R.3    Mosbach, K.4
  • 393
    • 0026331366 scopus 로고
    • Direct Enantioseparation of β-Adrenergic Blockers Using a Chiral Stationary Phase Prepared by Molecular Imprinting
    • Fischer, L.; Müller, R.; Ekberg, B.; Mosbach, K. Direct Enantioseparation of β-Adrenergic Blockers Using a Chiral Stationary Phase Prepared by Molecular Imprinting J. Am. Chem. Soc. 1991, 113, 9358-9360 10.1021/ja00024a046
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9358-9360
    • Fischer, L.1    Müller, R.2    Ekberg, B.3    Mosbach, K.4
  • 394
    • 0028196748 scopus 로고
    • Direct Resolution of Naproxen on a Non-Covalently Molecularly Imprinted Chiral Stationary Phase
    • Kempe, M.; Mosbach, K. Direct Resolution of Naproxen on a Non-Covalently Molecularly Imprinted Chiral Stationary Phase J. Chromatogr. A 1994, 664, 276-279 10.1016/0021-9673(94)87016-0
    • (1994) J. Chromatogr. A , vol.664 , pp. 276-279
    • Kempe, M.1    Mosbach, K.2
  • 395
    • 0031519297 scopus 로고    scopus 로고
    • Molecularly Imprinted Uniform-sized Polymer-based Stationary Phase for Naproxen
    • Haginaka, J.; Takehira, H.; Hosoya, K.; Tanaka, N. Molecularly Imprinted Uniform-sized Polymer-based Stationary Phase for Naproxen Chem. Lett. 1997, 555-556 10.1246/cl.1997.555
    • (1997) Chem. Lett. , pp. 555-556
    • Haginaka, J.1    Takehira, H.2    Hosoya, K.3    Tanaka, N.4
  • 396
    • 0000580345 scopus 로고
    • Molecular Recognition in Continuous Polymer Rods Prepared by a Molecular Imprinting Technique
    • Matui, J.; Kato, T.; Takeuchi, T.; Suzuki, M.; Yokoyama, K.; Tamiya, E.; Karube, I. Molecular Recognition in Continuous Polymer Rods Prepared by a Molecular Imprinting Technique Anal. Chem. 1993, 65, 2223-2224 10.1021/ac00065a009
    • (1993) Anal. Chem. , vol.65 , pp. 2223-2224
    • Matui, J.1    Kato, T.2    Takeuchi, T.3    Suzuki, M.4    Yokoyama, K.5    Tamiya, E.6    Karube, I.7
  • 397
    • 0028243087 scopus 로고
    • Imprinted Dispersion Polymers: A New Class of Easily Accessible Affinity Stationary Phases
    • Sellergren, B. Imprinted Dispersion Polymers: A New Class of Easily Accessible Affinity Stationary Phases J. Chromatogr. A 1994, 673, 133-141 10.1016/0021-9673(94)87066-7
    • (1994) J. Chromatogr. A , vol.673 , pp. 133-141
    • Sellergren, B.1
  • 398
    • 2942682672 scopus 로고    scopus 로고
    • Functional Mimicry of the Active Site of Carboxypeptidase A by a Molecular Imprinting Strategy: Cooperativity of an Amidinium and a Copper Ion in a Transition-State Imprinted Cavity Giving Rise to High Catalytic Activity
    • Liu, J. Q.; Wulff, G. Functional Mimicry of the Active Site of Carboxypeptidase A by a Molecular Imprinting Strategy: Cooperativity of an Amidinium and a Copper Ion in a Transition-State Imprinted Cavity Giving Rise to High Catalytic Activity J. Am. Chem. Soc. 2004, 126, 7452-7453 10.1021/ja048372l
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 7452-7453
    • Liu, J.Q.1    Wulff, G.2
  • 399
    • 45749109415 scopus 로고    scopus 로고
    • Functional Mimicry of Carboxypeptidase A by a Combination of Transition-State Stabilization and a Defined Orientation of Catalytic Moieties in Molecularly Imprinted Polymers
    • Liu, J. Q.; Wulff, G. Functional Mimicry of Carboxypeptidase A by a Combination of Transition-State Stabilization and a Defined Orientation of Catalytic Moieties in Molecularly Imprinted Polymers J. Am. Chem. Soc. 2008, 130, 8044-8054 10.1021/ja8012648
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 8044-8054
    • Liu, J.Q.1    Wulff, G.2
  • 400
    • 0026931265 scopus 로고
    • Ordered Mesoporous Molecular Sieves Synthesized by a Liquid-Crystal Template Mechanism
    • Kresge, C. T.; Leonowicz, M. E.; Roth, W. J.; Vartuli, J. C.; Beck, J. S. Ordered Mesoporous Molecular Sieves Synthesized by a Liquid-Crystal Template Mechanism Nature 1992, 359, 710-712 10.1038/359710a0
    • (1992) Nature , vol.359 , pp. 710-712
    • Kresge, C.T.1    Leonowicz, M.E.2    Roth, W.J.3    Vartuli, J.C.4    Beck, J.S.5
  • 401
    • 2542504379 scopus 로고    scopus 로고
    • Synthesis and Characterization of Chiral Mesoporous Silica
    • Che, S.; Liu, Z.; Ohsuna, T.; Sakamoto, K.; Terasaki, O.; Tatsumi, T. Synthesis and Characterization of Chiral Mesoporous Silica Nature 2004, 429, 281-284 10.1038/nature02529
    • (2004) Nature , vol.429 , pp. 281-284
    • Che, S.1    Liu, Z.2    Ohsuna, T.3    Sakamoto, K.4    Terasaki, O.5    Tatsumi, T.6
  • 402
    • 0013385076 scopus 로고    scopus 로고
    • From Microporous to Mesoporous Molecular Sieve Materials and their use in Catalysis
    • Corma, A. From Microporous to Mesoporous Molecular Sieve Materials and their use in Catalysis Chem. Rev. 1997, 97, 2373-2419 10.1021/cr960406n
    • (1997) Chem. Rev. , vol.97 , pp. 2373-2419
    • Corma, A.1
  • 403
    • 9644265391 scopus 로고    scopus 로고
    • Ordered Mesoporous Materials in Catalysis
    • Taguchi, A.; Schuth, F. Ordered Mesoporous Materials in Catalysis Microporous Mesoporous Mater. 2005, 77, 1-45 10.1016/j.micromeso.2004.06.030
    • (2005) Microporous Mesoporous Mater. , vol.77 , pp. 1-45
    • Taguchi, A.1    Schuth, F.2
  • 404
    • 34250821650 scopus 로고    scopus 로고
    • Efficient Bifunctional Nanocatalysts by Simple Postgrafting of Spatially Isolated Catalytic Groups on Mesoporous Materials
    • Sharma, K. K.; Asefa, T. Efficient Bifunctional Nanocatalysts by Simple Postgrafting of Spatially Isolated Catalytic Groups on Mesoporous Materials Angew. Chem., Int. Ed. 2007, 46, 2879-2882 10.1002/anie.200604570
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 2879-2882
    • Sharma, K.K.1    Asefa, T.2
  • 405
    • 84879523367 scopus 로고    scopus 로고
    • Micro-Mesoporous Materials Obtained by Zeolite Recrystallization: Synthesis, Characterization and Catalytic Applications
    • Ivanova, I. I.; Knyazeva, E. E. Micro-Mesoporous Materials Obtained by Zeolite Recrystallization: Synthesis, Characterization and Catalytic Applications Chem. Soc. Rev. 2013, 42, 3671-3688 10.1039/C2CS35341E
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 3671-3688
    • Ivanova, I.I.1    Knyazeva, E.E.2
  • 406
    • 84881319989 scopus 로고    scopus 로고
    • Mass Transfer in Mesoporous Materials: the Benefit of Microscopic Diffusion Measurement
    • Karger, J.; Valiullin, R. Mass Transfer in Mesoporous Materials: The Benefit of Microscopic Diffusion Measurement Chem. Soc. Rev. 2013, 42, 4172-4197 10.1039/c3cs35326e
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 4172-4197
    • Karger, J.1    Valiullin, R.2
  • 407
    • 0030602801 scopus 로고    scopus 로고
    • Comparison of an Ordered Mesoporous Aluminosilicate, Silica, Alumina, Titania and Zirconia in Normal-Phase High-Performance Liquid Chromatography
    • Grün, M.; Kurganov, A. A.; Schacht, S.; Schüth, F.; Unger, K. K. Comparison of an Ordered Mesoporous Aluminosilicate, Silica, Alumina, Titania and Zirconia in Normal-Phase High-Performance Liquid Chromatography J. Chromatogr. A 1996, 740, 1-9 10.1016/0021-9673(96)00205-1
    • (1996) J. Chromatogr. A , vol.740 , pp. 1-9
    • Grün, M.1    Kurganov, A.A.2    Schacht, S.3    Schüth, F.4    Unger, K.K.5
  • 409
    • 33747322047 scopus 로고    scopus 로고
    • Spherical Particles of Phenylene-Bridged Periodic Mesoporous Organosilica for High-Performance Liquid Chromatography
    • Rebbin, V.; Schmidt, R.; Fröba, M. Spherical Particles of Phenylene-Bridged Periodic Mesoporous Organosilica for High-Performance Liquid Chromatography Angew. Chem., Int. Ed. 2006, 45, 5210-5214 10.1002/anie.200504568
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 5210-5214
    • Rebbin, V.1    Schmidt, R.2    Fröba, M.3
  • 411
    • 0000131989 scopus 로고    scopus 로고
    • The Use of Mesoporous Silica in Liquid Chromatography
    • Gallis, K. W.; Araujo, J. T.; Duff, K. J.; Moore, J. G.; Landry, C. C. The Use of Mesoporous Silica in Liquid Chromatography Adv. Mater. 1999, 11, 1452-1455 10.1002/(SICI)1521-4095(199912)11:171452::AID-ADMA14523.3.CO;2-I
    • (1999) Adv. Mater. , vol.11 , pp. 1452-1455
    • Gallis, K.W.1    Araujo, J.T.2    Duff, K.J.3    Moore, J.G.4    Landry, C.C.5
  • 412
    • 0035297920 scopus 로고    scopus 로고
    • Spherical MSU-1 Mesoporous Silica Particles Tuned for HPLC
    • Boissière, C.; Kümmel, M.; Persin, M.; Larbot, A.; Prouzet, E. Spherical MSU-1 Mesoporous Silica Particles Tuned for HPLC Adv. Funct. Mater. 2001, 11, 129-135 10.1002/1616-3028(200104)11:2129::AID-ADFM1293.0.CO;2-W
    • (2001) Adv. Funct. Mater. , vol.11 , pp. 129-135
    • Boissière, C.1    Kümmel, M.2    Persin, M.3    Larbot, A.4    Prouzet, E.5
  • 413
    • 2342573630 scopus 로고    scopus 로고
    • Great Improvement of Chromatographic Performance Using MCM-41 Spheres as Stationary Phase in HPLC
    • Martin, T.; Galarneau, A.; Renzo, F. D.; Brunel, D.; Fajula, F.; Heinisch, S.; Cretier, G.; Rocca, J.-L. Great Improvement of Chromatographic Performance Using MCM-41 Spheres as Stationary Phase in HPLC Chem. Mater. 2004, 16, 1725-1731 10.1021/cm030443c
    • (2004) Chem. Mater. , vol.16 , pp. 1725-1731
    • Martin, T.1    Galarneau, A.2    Renzo, F.D.3    Brunel, D.4    Fajula, F.5    Heinisch, S.6    Cretier, G.7    Rocca, J.-L.8
  • 414
    • 0037035342 scopus 로고    scopus 로고
    • Biomolecule Separation Using Large Pore Mesoporous SBA-15 as a Substrate in High Performance Liquid Chromatography
    • Zhao, J. W.; Gao, F.; Fu, Y. L.; Jin, W.; Yang, P. Y.; Zhao, D. Y. Biomolecule Separation Using Large Pore Mesoporous SBA-15 as a Substrate in High Performance Liquid Chromatography Chem. Commun. 2002, 752-753 10.1039/b110637f
    • (2002) Chem. Commun. , pp. 752-753
    • Zhao, J.W.1    Gao, F.2    Fu, Y.L.3    Jin, W.4    Yang, P.Y.5    Zhao, D.Y.6
  • 416
    • 0000559355 scopus 로고
    • Chiral Nematic Suspensions of Cellulose Crystallites; Phase Separation and Magnetic Field Orientation
    • Revol, J. F.; Godbout, L.; Dong, X. M.; Gray, D. G.; Chanzy, H.; Maret, G. Chiral Nematic Suspensions of Cellulose Crystallites; Phase Separation and Magnetic Field Orientation Liq. Cryst. 1994, 16, 127-134 10.1080/02678299408036525
    • (1994) Liq. Cryst. , vol.16 , pp. 127-134
    • Revol, J.F.1    Godbout, L.2    Dong, X.M.3    Gray, D.G.4    Chanzy, H.5    Maret, G.6
  • 418
    • 78549265827 scopus 로고    scopus 로고
    • Free-Standing Mesoporous Silica Films with Tunable Chiral Nematic Structures
    • Shopsowitz, K. E.; Qi, H.; Hamad, W. Y.; MacLachlan, M. J. Free-Standing Mesoporous Silica Films with Tunable Chiral Nematic Structures Nature 2010, 468, 422-425 10.1038/nature09540
    • (2010) Nature , vol.468 , pp. 422-425
    • Shopsowitz, K.E.1    Qi, H.2    Hamad, W.Y.3    Maclachlan, M.J.4
  • 420
    • 84892801125 scopus 로고    scopus 로고
    • Biopolymer Templated Glass with a Twist: Controlling the Chirality, Porosity, and Photonic Properties of Silica with Cellulose Nanocrystals
    • Shopsowitz, K. E.; Kelly, J. A.; Hamad, W. Y.; MacLachlan, M. J. Biopolymer Templated Glass with a Twist: Controlling the Chirality, Porosity, and Photonic Properties of Silica with Cellulose Nanocrystals Adv. Funct. Mater. 2014, 24, 327-338 10.1002/adfm.201301737
    • (2014) Adv. Funct. Mater. , vol.24 , pp. 327-338
    • Shopsowitz, K.E.1    Kelly, J.A.2    Hamad, W.Y.3    Maclachlan, M.J.4
  • 421
    • 84898922307 scopus 로고    scopus 로고
    • Tunable Mesoporous Bilayer Photonic Resins with Chiral Nematic Structures and Actuator Properties
    • Khan, M. K.; Hamad, W. Y.; MacLachlan, M. J. Tunable Mesoporous Bilayer Photonic Resins with Chiral Nematic Structures and Actuator Properties Adv. Mater. 2014, 26, 2323-2328 10.1002/adma.201304966
    • (2014) Adv. Mater. , vol.26 , pp. 2323-2328
    • Khan, M.K.1    Hamad, W.Y.2    Maclachlan, M.J.3
  • 422
    • 84893877786 scopus 로고    scopus 로고
    • CdS Quantum Dots Encapsulated in Chiral Nematic Mesoporous Silica: New Iridescent and Luminescent Materials
    • Nguyen, T.-D.; Hamad, W. Y.; MacLachlan, M. J. CdS Quantum Dots Encapsulated in Chiral Nematic Mesoporous Silica: New Iridescent and Luminescent Materials Adv. Funct. Mater. 2014, 24, 777-783 10.1002/adfm.201302521
    • (2014) Adv. Funct. Mater. , vol.24 , pp. 777-783
    • Nguyen, T.-D.1    Hamad, W.Y.2    Maclachlan, M.J.3
  • 423
    • 0142138831 scopus 로고    scopus 로고
    • Silica Nanocasting of Simple Cellulose Derivatives: Towards Chiral Pore Systems with Long-Range Order and Chiral Optical Coatings
    • Thomas, A.; Antonietti, M. Silica Nanocasting of Simple Cellulose Derivatives: Towards Chiral Pore Systems with Long-Range Order and Chiral Optical Coatings Adv. Funct. Mater. 2003, 13, 763-766 10.1002/adfm.200304383
    • (2003) Adv. Funct. Mater. , vol.13 , pp. 763-766
    • Thomas, A.1    Antonietti, M.2
  • 424
    • 0037385910 scopus 로고    scopus 로고
    • Synthesis of Mesoporous Silica by Sol-Gel Mineralisation of Cellulose Nanorod Nematic Suspensions
    • Dujardin, E.; Blaseby, M.; Mann, S. Synthesis of Mesoporous Silica by Sol-Gel Mineralisation of Cellulose Nanorod Nematic Suspensions J. Mater. Chem. 2003, 13, 696-699 10.1039/b212689c
    • (2003) J. Mater. Chem. , vol.13 , pp. 696-699
    • Dujardin, E.1    Blaseby, M.2    Mann, S.3
  • 425
    • 84907903195 scopus 로고    scopus 로고
    • Novel Inorganic Mesoporous Material with Chiral Nematic Structure Derived from Nanocrystalline Cellulose for High-Resolution Gas Chromatographic Separations
    • Zhang, J.-H.; Xie, S.-M.; Zhang, M.; Zi, M.; He, P.-G.; Yuan, L.-M. Novel Inorganic Mesoporous Material with Chiral Nematic Structure Derived from Nanocrystalline Cellulose for High-Resolution Gas Chromatographic Separations Anal. Chem. 2014, 86, 9595-9602 10.1021/ac502073g
    • (2014) Anal. Chem. , vol.86 , pp. 9595-9602
    • Zhang, J.-H.1    Xie, S.-M.2    Zhang, M.3    Zi, M.4    He, P.-G.5    Yuan, L.-M.6
  • 426
    • 0037127013 scopus 로고    scopus 로고
    • Systematic Design of Pore Size and Functionality in Isoreticular MOFs and their Application in Methane Storage
    • Eddaoudi, M.; Kim, J.; Rosi, N.; Vodak, D.; Wachter, J.; O'Keeffe, M.; Yaghi, O. M. Systematic Design of Pore Size and Functionality in Isoreticular MOFs and their Application in Methane Storage Science 2002, 295, 469-472 10.1126/science.1067208
    • (2002) Science , vol.295 , pp. 469-472
    • Eddaoudi, M.1    Kim, J.2    Rosi, N.3    Vodak, D.4    Wachter, J.5    O'Keeffe, M.6    Yaghi, O.M.7
  • 427
    • 8344285762 scopus 로고    scopus 로고
    • Hysteretic Adsorption and Desorption of Hydrogen by Nanoporous Metal-Organic Frameworks
    • Zhao, X.; Xiao, B.; Fletcher, A. J.; Thomas, K. M.; Bradshaw, D.; Rosseinsky, M. J. Hysteretic Adsorption and Desorption of Hydrogen by Nanoporous Metal-Organic Frameworks Science 2004, 306, 1012-1015 10.1126/science.1101982
    • (2004) Science , vol.306 , pp. 1012-1015
    • Zhao, X.1    Xiao, B.2    Fletcher, A.J.3    Thomas, K.M.4    Bradshaw, D.5    Rosseinsky, M.J.6
  • 428
    • 23044451308 scopus 로고    scopus 로고
    • Strategies for Hydrogen Storage in Metal-Organic Frameworks
    • Rowsell, J. L. C.; Yaghi, O. M. Strategies for Hydrogen Storage in Metal-Organic Frameworks Angew. Chem., Int. Ed. 2005, 44, 4670-4679 10.1002/anie.200462786
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 4670-4679
    • Rowsell, J.L.C.1    Yaghi, O.M.2
  • 429
    • 77954858634 scopus 로고    scopus 로고
    • An Isoreticular Series of Metal-Organic Frameworks with Dendritic Hexacarboxylate Ligands and Exceptionally High Gas-Uptake Capacity
    • Yuan, D.; Zhao, D.; Sun, D.; Zhou, H.-C. An Isoreticular Series of Metal-Organic Frameworks with Dendritic Hexacarboxylate Ligands and Exceptionally High Gas-Uptake Capacity Angew. Chem., Int. Ed. 2010, 49, 5357-5361 10.1002/anie.201001009
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 5357-5361
    • Yuan, D.1    Zhao, D.2    Sun, D.3    Zhou, H.-C.4
  • 430
    • 4544324529 scopus 로고    scopus 로고
    • A Robust Porous Material Constructed of Linear Coordination Polymer Chains: Reversible Single-Crystal to Single-Crystal Transformations upon Dehydration and Rehydration
    • Lee, E. Y.; Suh, M. P. A Robust Porous Material Constructed of Linear Coordination Polymer Chains: Reversible Single-Crystal to Single-Crystal Transformations upon Dehydration and Rehydration Angew. Chem., Int. Ed. 2004, 43, 2798-2801 10.1002/anie.200353494
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 2798-2801
    • Lee, E.Y.1    Suh, M.P.2
  • 431
    • 65349158272 scopus 로고    scopus 로고
    • Selective Gas Adsorption and Separation in Metal-Organic Frameworks
    • Li, J.-R.; Kuppler, R. J.; Zhou, H.-C. Selective Gas Adsorption and Separation in Metal-Organic Frameworks Chem. Soc. Rev. 2009, 38, 1477-1504 10.1039/b802426j
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 1477-1504
    • Li, J.-R.1    Kuppler, R.J.2    Zhou, H.-C.3
  • 432
    • 79953675712 scopus 로고    scopus 로고
    • Kinetic Separation of Propene and Propane in Metal-Organic Frameworks: Controlling Diffusion Rates in Plate-Shaped Crystals via Tuning of Pore Apertures and Crystallite Aspect Ratios
    • Lee, C. Y.; Bae, Y.-S.; Jeong, N. C.; Farha, O. K.; Sarjeant, A. A.; Stern, C. L.; Nichias, P.; Snurr, R. Q.; Hupp, J. T.; Nguyen, S. T. Kinetic Separation of Propene and Propane in Metal-Organic Frameworks: Controlling Diffusion Rates in Plate-Shaped Crystals via Tuning of Pore Apertures and Crystallite Aspect Ratios J. Am. Chem. Soc. 2011, 133, 5228-5231 10.1021/ja200553m
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 5228-5231
    • Lee, C.Y.1    Bae, Y.-S.2    Jeong, N.C.3    Farha, O.K.4    Sarjeant, A.A.5    Stern, C.L.6    Nichias, P.7    Snurr, R.Q.8    Hupp, J.T.9    Nguyen, S.T.10
  • 433
    • 0001412882 scopus 로고    scopus 로고
    • A Homochiral Metal-Organic Porous Material for Enantioselective Separation and Catalysis
    • Seo, J. S.; Whang, D.; Lee, H.; Jun, S. I.; Oh, J.; Jeon, Y. J.; Kim, K. A Homochiral Metal-Organic Porous Material for Enantioselective Separation and Catalysis Nature 2000, 404, 982-986 10.1038/35010088
    • (2000) Nature , vol.404 , pp. 982-986
    • Seo, J.S.1    Whang, D.2    Lee, H.3    Jun, S.I.4    Oh, J.5    Jeon, Y.J.6    Kim, K.7
  • 434
    • 21244446924 scopus 로고    scopus 로고
    • A Homochiral Porous Metal-Organic Framework for Highly Enantioselective Heterogeneous Asymmetric Catalysis
    • Wu, C. D.; Hu, A.; Zhang, L.; Lin, W. B. A Homochiral Porous Metal-Organic Framework for Highly Enantioselective Heterogeneous Asymmetric Catalysis J. Am. Chem. Soc. 2005, 127, 8940-8941 10.1021/ja052431t
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 8940-8941
    • Wu, C.D.1    Hu, A.2    Zhang, L.3    Lin, W.B.4
  • 436
    • 77954063984 scopus 로고    scopus 로고
    • Engineering Metal Organic Frameworks for Heterogeneous Catalysis
    • Corma, A.; Garcia, H.; Xamena, F. X. L. Engineering Metal Organic Frameworks for Heterogeneous Catalysis Chem. Rev. 2010, 110, 4606-4655 10.1021/cr9003924
    • (2010) Chem. Rev. , vol.110 , pp. 4606-4655
    • Corma, A.1    Garcia, H.2    Xamena, F.X.L.3
  • 437
    • 35848970318 scopus 로고    scopus 로고
    • Enantioselective Chromatographic Resolution and One-Pot Synthesis of Enantiomerically Pure Sulfoxides over a Homochiral Zn-Organic Framework
    • Nuzhdin, A. L.; Dybtsev, D. N.; Bryliakov, K. P.; Talsi, E. P.; Fedin, V. P. Enantioselective Chromatographic Resolution and One-Pot Synthesis of Enantiomerically Pure Sulfoxides over a Homochiral Zn-Organic Framework J. Am. Chem. Soc. 2007, 129, 12958-12959 10.1021/ja076276p
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12958-12959
    • Nuzhdin, A.L.1    Dybtsev, D.N.2    Bryliakov, K.P.3    Talsi, E.P.4    Fedin, V.P.5
  • 439
    • 78049360703 scopus 로고    scopus 로고
    • Separation of Styrene and Ethylbenzene on Metal-Organic Frameworks: Analogous Structures with Different Adsorption Mechanisms
    • Maes, M.; Alaerts, L.; Couck, S.; Kirschhock, C. E. A.; Denayer, J. F. M.; Vos, D. E. D. Separation of Styrene and Ethylbenzene on Metal-Organic Frameworks: Analogous Structures with Different Adsorption Mechanisms J. Am. Chem. Soc. 2010, 132, 15277-15285 10.1021/ja106142x
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15277-15285
    • Maes, M.1    Alaerts, L.2    Couck, S.3    Kirschhock, C.E.A.4    Denayer, J.F.M.5    Vos, D.E.D.6
  • 440
    • 77957563058 scopus 로고    scopus 로고
    • Engineering Homochiral Metal-Organic Frameworks for Heterogeneous Asymmetric Catalysis and Enantioselective Separation
    • Liu, Y.; Xuan, W.; Cui, Y. Engineering Homochiral Metal-Organic Frameworks for Heterogeneous Asymmetric Catalysis and Enantioselective Separation Adv. Mater. 2010, 22, 4112-4135 10.1002/adma.201000197
    • (2010) Adv. Mater. , vol.22 , pp. 4112-4135
    • Liu, Y.1    Xuan, W.2    Cui, Y.3
  • 441
    • 77957315730 scopus 로고    scopus 로고
    • Zeolitic Imidazolate Framework-8 Nanocrystal Coated Capillary for Molecular Sieving of Branched Alkanes from Linear Alkanes Along with High-Resolution Chromatographic Separation of Linear Alkanes
    • Chang, N.; Gu, Z. Y.; Yan, X. P. Zeolitic Imidazolate Framework-8 Nanocrystal Coated Capillary for Molecular Sieving of Branched Alkanes from Linear Alkanes Along with High-Resolution Chromatographic Separation of Linear Alkanes J. Am. Chem. Soc. 2010, 132, 13645-13647 10.1021/ja1058229
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 13645-13647
    • Chang, N.1    Gu, Z.Y.2    Yan, X.P.3
  • 442
    • 79961149897 scopus 로고    scopus 로고
    • Chiral Metal-Organic Frameworks for High-Resolution Gas Chromatographic Separations
    • Xie, S.-M.; Zhang, Z.-J.; Wang, Z.-Y.; Yuan, L.-M. Chiral Metal-Organic Frameworks for High-Resolution Gas Chromatographic Separations J. Am. Chem. Soc. 2011, 133, 11892-12895 10.1021/ja2044453
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 11892-12895
    • Xie, S.-M.1    Zhang, Z.-J.2    Wang, Z.-Y.3    Yuan, L.-M.4
  • 443
    • 84892766884 scopus 로고    scopus 로고
    • High-Performance Liquid Chromatographic Enantioseparation of Racemic Drugs Based on Homochiral Metal-Organic Framework
    • Kuang, X.; Ma, Y.; Su, H.; Zhang, J.; Dong, Y.-B.; Tang, B. High-Performance Liquid Chromatographic Enantioseparation of Racemic Drugs Based on Homochiral Metal-Organic Framework Anal. Chem. 2014, 86, 1277-1281 10.1021/ac403674p
    • (2014) Anal. Chem. , vol.86 , pp. 1277-1281
    • Kuang, X.1    Ma, Y.2    Su, H.3    Zhang, J.4    Dong, Y.-B.5    Tang, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.