메뉴 건너뛰기




Volumn , Issue , 2006, Pages 987-1051

Chiral Separations

Author keywords

Chiral separation; Mixed types of interaction; Molecular interactions

Indexed keywords


EID: 84889372331     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9780470087954.ch22     Document Type: Chapter
Times cited : (7)

References (164)
  • 1
    • 77956707367 scopus 로고
    • The history of enantiomeric resolution
    • in M. Zief and L. J. Crane (eds.), Marcel Dekker, New York
    • B. Feibush and N. Grinberg, The history of enantiomeric resolution, in M. Zief and L. J. Crane (eds.), Chromatographic Chiral Separations, Marcel Dekker, New York, 1988, p. 1.
    • (1988) Chromatographic Chiral Separations , pp. 1
    • Feibush, B.1    Grinberg, N.2
  • 2
    • 0001911122 scopus 로고
    • The optical resolution of aromatic amino acids on paper chromatograms
    • C. E. Dalgliesh, The optical resolution of aromatic amino acids on paper chromatograms. J. Chem. Soc. (1952), 3940.
    • (1952) J. Chem. Soc. , pp. 3940
    • Dalgliesh, C.E.1
  • 3
    • 0004031703 scopus 로고
    • Chromatographic Enantioseparation. Methods and Applications
    • John Wiley & Sons, New York
    • S. G. Allenmark, Chromatographic Enantioseparation. Methods and Applications, John Wiley & Sons, New York, 1988, p. 13.
    • (1988) , pp. 13
    • Allenmark, S.G.1
  • 4
    • 39149140764 scopus 로고
    • Separation of enantiomers by gas chromatography with an optically active stationary phase
    • E. Gil-Av, B. Feibush, and R. Charles-Sigler, Separation of enantiomers by gas chromatography with an optically active stationary phase,Tetrahedron Lett. 7 (1966), 1009.
    • (1966) Tetrahedron Lett. , vol.7 , pp. 1009
    • Gil-Av, E.1    Feibush, B.2    Charles-Sigler, R.3
  • 5
    • 0006922828 scopus 로고
    • Theory and design of chiral stationary phases for direct chromatographic separation of enantiomers
    • in K. K. Unger (ed.), Marcel Dekker, New York
    • W. H. Pirkle and T. C. Pochapsky, Theory and design of chiral stationary phases for direct chromatographic separation of enantiomers, in K. K. Unger (ed.), Packings and Stationary Phases in Chromatographic Techniques, Marcel Dekker, New York, 1990, p. 783.
    • (1990) Packings and Stationary Phases in Chromatographic Techniques , pp. 783
    • Pirkle, W.H.1    Pochapsky, T.C.2
  • 6
    • 0002226189 scopus 로고
    • Indirect methods for the chromatographic resolution of drug enantiomers
    • in I.W.Wainer (ed.), Marcel Dekker, New York
    • J. Gal, Indirect methods for the chromatographic resolution of drug enantiomers, in I.W.Wainer (ed.), Drug Stereochemistry Analytical Methods and Pharmacology, Marcel Dekker, New York, 1993, pp. 65-106.
    • (1993) Drug Stereochemistry Analytical Methods and Pharmacology , pp. 65-106
    • Gal, J.1
  • 7
    • 0002392994 scopus 로고
    • Indirect separation of enantiomers by liquid chromatography
    • in M. Zief and L. J. Crane (eds.), Marcel Dekker, New York
    • W. Lindner, Indirect separation of enantiomers by liquid chromatography, in M. Zief and L. J. Crane (eds.), Chromatographic Chiral Separation, Marcel Dekker, New York, 1988, pp. 91-130.
    • (1988) Chromatographic Chiral Separation , pp. 91-130
    • Lindner, W.1
  • 8
    • 0031823257 scopus 로고    scopus 로고
    • Chiral separation of enantiomers via selector/selectand hydrogen bondings
    • B. Feibush, Chiral separation of enantiomers via selector/selectand hydrogen bondings, Chirality 10 (1998), 382-395.
    • (1998) Chirality , vol.10 , pp. 382-395
    • Feibush, B.1
  • 9
    • 49749200051 scopus 로고
    • Gas chromatographic evidence for intramolecular hydrogen bonding with double bonds
    • C. H. DePuy and P. R. Story, Gas chromatographic evidence for intramolecular hydrogen bonding with double bonds, Tetrahedron Lett 1 (1959), 20.
    • (1959) Tetrahedron Lett , vol.1 , pp. 20
    • DePuy, C.H.1    Story, P.R.2
  • 10
    • 84943489727 scopus 로고
    • Separation of diastereomers by gas-liquid chromatography: Esters of butane-2,3-diol
    • D. Nurok, G. L. Taylor, and A. M. Stephen, Separation of diastereomers by gas-liquid chromatography: Esters of butane-2,3-diol, J. Chem. Soc. B (1968), 291.
    • (1968) J. Chem. Soc. B , pp. 291
    • Nurok, D.1    Taylor, G.L.2    Stephen, A.M.3
  • 11
    • 33947458960 scopus 로고
    • The Hydrogen bond. I. Intra- and intermolecular hydrogen bonds in alcohols
    • L. P. Kuhn, The Hydrogen bond. I. Intra- and intermolecular hydrogen bonds in alcohols. J. Am. Chem. Soc. 74 (1952), 2492.
    • (1952) J. Am. Chem. Soc. , vol.74 , pp. 2492
    • Kuhn, L.P.1
  • 12
    • 84912204672 scopus 로고
    • Separation d'alcools acycliques diastereomeres par chromatographie gaseuse
    • Y. Gault and H. Felkin, Separation d'alcools acycliques diastereomeres par chromatographie gaseuse, Bull. Soc. Chim. France 3 (1965), 742.
    • (1965) Bull. Soc. Chim. France , vol.3 , pp. 742
    • Gault, Y.1    Felkin, H.2
  • 13
    • 0041491445 scopus 로고
    • Resolution of optical isomers by gas chromatography of diastereomers
    • Advances in Chromatography, J. C. Giddings and R. A. Keller (eds.), Marcel Dekker, New York
    • E. Gil-Av and D. Nurok, Resolution of optical isomers by gas chromatography of diastereomers, in Advances in Chromatography, J. C. Giddings and R. A. Keller (eds.), Marcel Dekker, New York, 1974, pp. 99-172.
    • (1974) , pp. 99-172
    • Gil-Av, E.1    Nurok, D.2
  • 14
    • 0011833748 scopus 로고
    • Studies on the mechanism of separation of diastereomeric esters by gas-liquid chromatography; effect of bulk dissymmetry and distance between the optical centers
    • H. C. Rose, R. L. Stern, and B. L. Karger, Studies on the mechanism of separation of diastereomeric esters by gas-liquid chromatography; effect of bulk dissymmetry and distance between the optical centers, Anal. Chem. 38 (1966), 469.
    • (1966) Anal. Chem. , vol.38 , pp. 469
    • Rose, H.C.1    Stern, R.L.2    Karger, B.L.3
  • 15
    • 4244136259 scopus 로고
    • Gas-liquid chromatographic separation of diastereomeric amides of racemic cyclic amines
    • B. L. Karger, R. L. Stern, and W. Keanr, Gas-liquid chromatographic separation of diastereomeric amides of racemic cyclic amines, Anal. Chem. 39 (1967), 228.
    • (1967) Anal. Chem. , vol.39 , pp. 228
    • Karger, B.L.1    Stern, R.L.2    Keanr, W.3
  • 16
    • 0001989412 scopus 로고
    • Interpretation and correlation of bulkiness chirality and separation coefficients in the resolution of diastereomers by gas-chromatography
    • B. Feibush, Interpretation and correlation of bulkiness chirality and separation coefficients in the resolution of diastereomers by gas-chromatography, Anal. Chem. 43 (1971), 1098.
    • (1971) Anal. Chem. , vol.43 , pp. 1098
    • Feibush, B.1
  • 17
    • 0011265223 scopus 로고
    • Separation of enantiomers by liquid chromatographic methods
    • in J.D. Morrison (ed.), Analytical Methods, Academic Press: New York
    • W. H. Pirkle and J. Finn, Separation of enantiomers by liquid chromatographic methods, in J.D. Morrison (ed.), Asymmetric Synthesis,Vol. 1, Analytical Methods, Academic Press: New York, 1983, pp. 87-124.
    • (1983) Asymmetric Synthesis , vol.1 , pp. 87-124
    • Pirkle, W.H.1    Finn, J.2
  • 18
    • 84966111242 scopus 로고
    • Extreme liquid chromatographic separation effects in the case of diastereomeric amides containing polar substituents
    • G. Helmchen,G. Nill,D. Flockerzi,W. Schuhle, and M. S. K.Yousef, Extreme liquid chromatographic separation effects in the case of diastereomeric amides containing polar substituents, Angew. Chem. Int. Ed. Engl. 18 (1979), 62.
    • (1979) Angew. Chem. Int. Ed. Engl. , vol.18 , pp. 62
    • Helmchen, G.1    Nill, G.2    Flockerzi, D.3    Schuhle, W.4    Yousef, M.S.K.5
  • 19
    • 2642684241 scopus 로고
    • Separation of enantiomers by asymmetric phases in gas liquid chromatography
    • Ph.D thesis, The Weizmann Institute of Science, Rehovot, Israel
    • B. Feibush, Separation of enantiomers by asymmetric phases in gas liquid chromatography, Ph.D thesis, 1967, The Weizmann Institute of Science, Rehovot, Israel.
    • (1967)
    • Feibush, B.1
  • 20
    • 0030933019 scopus 로고    scopus 로고
    • The nature of chiral recognition: Is it a three-point interaction
    • V. A. Davankov, The nature of chiral recognition: Is it a three-point interaction? Chirality 9 (1997), 99.
    • (1997) Chirality , vol.9 , pp. 99
    • Davankov, V.A.1
  • 21
    • 0030896847 scopus 로고    scopus 로고
    • On the minimum requirements of chiral recognition
    • W. H. Pirkle, On the minimum requirements of chiral recognition. Chirality 9 (1997), 103.
    • (1997) Chirality , vol.9 , pp. 103
    • Pirkle, W.H.1
  • 22
    • 0030936156 scopus 로고    scopus 로고
    • Is chiral recognition a three point process
    • T. D. Booth, D. Wahnon, and I. W. Wainer, Is chiral recognition a three point process? Chirality 9 (1997), 96.
    • (1997) Chirality , vol.9 , pp. 96
    • Booth, T.D.1    Wahnon, D.2    Wainer, I.W.3
  • 23
    • 21844454445 scopus 로고    scopus 로고
    • Biological chiral recognition: The substrate's perspective
    • V. Sundaresan and R. Abrol, Biological chiral recognition: The substrate's perspective, Chirality 17 (2005), S30.
    • (2005) Chirality , vol.17
    • Sundaresan, V.1    Abrol, R.2
  • 25
    • 0031823257 scopus 로고    scopus 로고
    • Chiral separation of enantiomers via selector/selectand hydrogen bondings
    • B. Feibush, Chiral separation of enantiomers via selector/selectand hydrogen bondings, Chirality 10 (1998), 382.
    • (1998) Chirality , vol.10 , pp. 382
    • Feibush, B.1
  • 26
    • 0024834111 scopus 로고
    • A general criterion for molecular recognition: Implications for chiral interactions
    • S. Topiol, A general criterion for molecular recognition: Implications for chiral interactions, Chirality 1 (1989), 69.
    • (1989) Chirality , vol.1 , pp. 69
    • Topiol, S.1
  • 27
    • 0003914038 scopus 로고    scopus 로고
    • An Introduction to Hydrogen Bonding
    • Oxford University Press, New York
    • G. J. Jeffrey, An Introduction to Hydrogen Bonding, Oxford University Press, New York, 1997, p. 11.
    • (1997) , pp. 11
    • Jeffrey, G.J.1
  • 28
    • 0001497206 scopus 로고
    • X-ray and neutron diffraction studies of hydrogen bonded systems
    • in P. Schuster, G. Zundel, and C. Sandorfy (eds.), Recent Developments in Theory and Experiments. II. Structure and Spectroscopy, Vol. II, North Holland, Amsterdam
    • I. Olovsson and P.-G. Jonsson, X-ray and neutron diffraction studies of hydrogen bonded systems, in P. Schuster, G. Zundel, and C. Sandorfy (eds.), The Hydrogen Bond. Recent Developments in Theory and Experiments. II. Structure and Spectroscopy, Vol. II, North Holland, Amsterdam, 1976, p. 393.
    • (1976) The Hydrogen Bond. , pp. 393
    • Olovsson, I.1    Jonsson, P.-G.2
  • 30
    • 0001439119 scopus 로고
    • Easily polarizable hydrogen bonds-their interactions with the environment- ir continuum and anomalous large proton conductivity
    • in P. Schuster, G. Zundel, and C. Sandorfy The Hydrogen Bond. Recent Developments in Theory and Experiments. II. Structure and Spectroscopy, Vol. II, North Holland, Amsterdam
    • G. Zundel, Easily polarizable hydrogen bonds-their interactions with the environment- ir continuum and anomalous large proton conductivity, in P. Schuster, G. Zundel, and C. Sandorfy The Hydrogen Bond. Recent Developments in Theory and Experiments. II. Structure and Spectroscopy, Vol. II, North Holland, Amsterdam, 1976, p. 683.
    • (1976) , pp. 683
    • Zundel, G.1
  • 31
    • 0004140795 scopus 로고
    • Proteins Structure and Molecular Properties
    • W.H. Freeman, New York
    • T. E. Creighton, Proteins Structure and Molecular Properties, W.H. Freeman, New York, 1993, p. 5.
    • (1993) , pp. 5
    • Creighton, T.E.1
  • 32
    • 0019267144 scopus 로고
    • Intramolecular hidrogen-bonded peptide conformations
    • C. Toniolo, Intramolecular hidrogen-bonded peptide conformations, CRC Crit. Rev. Biochem. 9 (1980), 1.
    • (1980) CRC Crit. Rev. Biochem. , vol.9 , pp. 1
    • Toniolo, C.1
  • 33
    • 39149140764 scopus 로고
    • Separation of enantiomers by GLC with an optical active stationary phase
    • E. Gil-Av, B. Feibush, and R. Cherles-Sigler, Separation of enantiomers by GLC with an optical active stationary phase, Tetrahedron Lett. 10 (1966), 1009.
    • (1966) Tetrahedron Lett. , vol.10 , pp. 1009
    • Gil-Av, E.1    Feibush, B.2    Cherles-Sigler, R.3
  • 34
    • 0014757146 scopus 로고
    • Interaction between asymmetric solutes and solvents. Peptide derivatives as stationary phases in gas liquid partition chromatography
    • B. Feibush and E. Gil-Av, Interaction between asymmetric solutes and solvents. Peptide derivatives as stationary phases in gas liquid partition chromatography, Tetrahedron 26 (1970), 1361.
    • (1970) Tetrahedron , vol.26 , pp. 1361
    • Feibush, B.1    Gil-Av, E.2
  • 35
    • 0017312795 scopus 로고
    • Interaction between asymmetric solutes and solvents. Peptide derivatives as stationary phases in gas-liquid partition chromatography
    • U. Beitler and B. Feibush, Interaction between asymmetric solutes and solvents. Peptide derivatives as stationary phases in gas-liquid partition chromatography, J. Chromatogr. 123 (1976), 149.
    • (1976) J. Chromatogr. , vol.123 , pp. 149
    • Beitler, U.1    Feibush, B.2
  • 36
    • 37049101733 scopus 로고
    • Chiral solute-solvent systems. Selective interaction between N-lauroyl-l-valine amides and N-trifluoroactyl esters of enantiomers of 2-amino-alkan-1-olsα-, β-, and γ-amino acids
    • B. Feibush, A. Balan, B. Altman, and E. Gil-Av, Chiral solute-solvent systems. Selective interaction between N-lauroyl-l-valine amides and N-trifluoroactyl esters of enantiomers of 2-amino-alkan-1-ols, α-, β-, and γ-amino acids, J. Chem. Soc. Perkin Trans II 9 (1979), 1230.
    • (1979) J. Chem. Soc. Perkin Trans II , vol.9 , pp. 1230
    • Feibush, B.1    Balan, A.2    Altman, B.3    Gil-Av, E.4
  • 37
    • 33744986566 scopus 로고
    • Chiral recognition in gas cgromatographic analysis of enantiomers on chiral polysiloxanes
    • B. Koppenhoefer and E. Bayer, Chiral recognition in gas cgromatographic analysis of enantiomers on chiral polysiloxanes. J. Chromatogr. Library 32 (1985), 1.
    • (1985) J. Chromatogr. Library , vol.32 , pp. 1
    • Koppenhoefer, B.1    Bayer, E.2
  • 38
    • 0000383098 scopus 로고
    • Chiral recognition in the resolution of enantiomers by GLC
    • B. Koppenhoefer and E. Bayer, Chiral recognition in the resolution of enantiomers by GLC, Chromatographia 19 (1984), 123.
    • (1984) Chromatographia , vol.19 , pp. 123
    • Koppenhoefer, B.1    Bayer, E.2
  • 39
    • 33845379431 scopus 로고
    • Extended scope of chiral recognition applying hydrogen bond association in nonaqueous media (R,R)-N,N'-disopropyltartaramide (DIPTA) as a widely applicable resolving agent
    • Y. Dobashi and S. Hara, Extended scope of chiral recognition applying hydrogen bond association in nonaqueous media (R,R)-N,N'-disopropyltartaramide (DIPTA) as a widely applicable resolving agent, J. Am. Chem. Soc. 107 (1985), 3406.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 3406
    • Dobashi, Y.1    Hara, S.2
  • 40
    • 0001389993 scopus 로고
    • A chiral stationary phase derived from (R,R)-tartramide with broaden scope of application to the liquid chromatographic resolution of enantiomers
    • Y. Dobashi and S. Hara, A chiral stationary phase derived from (R,R)-tartramide with broaden scope of application to the liquid chromatographic resolution of enantiomers, J. Org. Chem. 52 (1987), 2490.
    • (1987) J. Org. Chem. , vol.52 , pp. 2490
    • Dobashi, Y.1    Hara, S.2
  • 41
    • 0003172241 scopus 로고
    • New chiral polysiloxane derived from (R,R)-tartramide for enantiomer resolution by capillary gas chromatography
    • Y. Dobashi, K. Nakamura, T. Saeki, M. Matsuo, S. Hara, and A. Dobashi, New chiral polysiloxane derived from (R,R)-tartramide for enantiomer resolution by capillary gas chromatography, J. Org. Chem. 56 (1991), 3299.
    • (1991) J. Org. Chem. , vol.56 , pp. 3299
    • Dobashi, Y.1    Nakamura, K.2    Saeki, T.3    Matsuo, M.4    Hara, S.5    Dobashi, A.6
  • 42
    • 0030576511 scopus 로고    scopus 로고
    • Chromatographic separation of enantiomers on N,N'-diallyl-L-tartardiamide-based network-Polymeric chiral stationary phases
    • S. Anderson, S. Allenmark, P. Moller, B. Persson, and D. Sanchez, Chromatographic separation of enantiomers on N,N'-diallyl-L-tartardiamide-based network-Polymeric chiral stationary phases, J. Chromatogr. 741 (1996), 23.
    • (1996) J. Chromatogr. , vol.741 , pp. 23
    • Anderson, S.1    Allenmark, S.2    Moller, P.3    Persson, B.4    Sanchez, D.5
  • 43
    • 0022624282 scopus 로고
    • Chromatographic resolution of chiral drugs on polyamides and cellulose triacetate
    • G. Blaschke, Chromatographic resolution of chiral drugs on polyamides and cellulose triacetate, J. Liq. Chromatogr. 9 (1986), 341.
    • (1986) J. Liq. Chromatogr. , vol.9 , pp. 341
    • Blaschke, G.1
  • 44
    • 0346966418 scopus 로고
    • Substituted polyacrylamides as chiral phases for the resolution of drugs
    • M. Zieff and L. J. Crane (eds.), Marcel Dekker, New York
    • G. Blaschke, Substituted polyacrylamides as chiral phases for the resolution of drugs, in Chromatographic Chiral Separation, M. Zieff and L. J. Crane (eds.), Marcel Dekker, New York, 1988, p. 179.
    • (1988) Chromatographic Chiral Separation , pp. 179
    • Blaschke, G.1
  • 45
    • 0022535581 scopus 로고
    • Chiral separation of heterocyclic drugs by HPLC: Solute-stationary phase base-pair interactions
    • B. Feibush, A. Figueroa, R. Charles, K. Onan, P. Feibush, and B. L. Karger, Chiral separation of heterocyclic drugs by HPLC: Solute-stationary phase base-pair interactions, J. Am. Chem. Soc. 108 (1986), 3310.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 3310
    • Feibush, B.1    Figueroa, A.2    Charles, R.3    Onan, K.4    Feibush, P.5    Karger, B.L.6
  • 46
    • 33845378119 scopus 로고
    • Host-guest complexation. 36. Spherand and litium and sodium complexation rates equilibria
    • D. J. Cram and G. M. Lein, Host-guest complexation. 36. Spherand and litium and sodium complexation rates equilibria, J. Am. Chem. Soc. 107 (1985), 3657.
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 3657
    • Cram, D.J.1    Lein, G.M.2
  • 47
    • 0004031703 scopus 로고
    • Chromatographic Enantioseparation Methods and Applications
    • Ellis Horwood, New York
    • S. G. Allenmark, Chromatographic Enantioseparation Methods and Applications, Ellis Horwood, New York, 1988, p. 69.
    • (1988) , pp. 69
    • Allenmark, S.G.1
  • 48
    • 84985609923 scopus 로고
    • Cyclodextrin inclusion compounds in research and industry
    • W. Saenger, Cyclodextrin inclusion compounds in research and industry, Angew. Chem. Int. Ed. 19 (1980), 344.
    • (1980) Angew. Chem. Int. Ed. , vol.19 , pp. 344
    • Saenger, W.1
  • 50
    • 0022498516 scopus 로고
    • Separation of drug stereoisomers by formation of β-cyclodextrin inclusion complexes
    • D. W. Armstrong, T. J. Ward, R. D. Armstrong, and T. E. Beesley, Separation of drug stereoisomers by formation of β-cyclodextrin inclusion complexes, Science 232 (1986), 1132.
    • (1986) Science , vol.232 , pp. 1132
    • Armstrong, D.W.1    Ward, T.J.2    Armstrong, R.D.3    Beesley, T.E.4
  • 51
    • 0000319162 scopus 로고
    • Structural factors affecting the chiral recognition and separation on β-cyclodextrin bonded phase
    • S. M. Han, Y. I. Han, and D.W. Armstrong, Structural factors affecting the chiral recognition and separation on β-cyclodextrin bonded phase, J. Chromatogr. 441 (1988), 376.
    • (1988) J. Chromatogr. , vol.441 , pp. 376
    • Han, S.M.1    Han, Y.I.2    Armstrong, D.W.3
  • 52
    • 0022011425 scopus 로고
    • Separation of metallocene enantiomers by liquid chromatography: Chiral recognition via cyclodextrin bonded phases
    • D.W. Armstrong,W. DeMond, and B. P. Czech, Separation of metallocene enantiomers by liquid chromatography: Chiral recognition via cyclodextrin bonded phases, Anal. Chem. 57 (1985), 481.
    • (1985) Anal. Chem. , vol.57 , pp. 481
    • Armstrong, D.W.1    DeMond, W.2    Czech, B.P.3
  • 53
    • 0007233796 scopus 로고    scopus 로고
    • Structural aspects of stereodiscrimination in the solid state
    • K. Harata, Structural aspects of stereodiscrimination in the solid state, Chem. Rev. 98 (1998), 1803.
    • (1998) Chem. Rev. , vol.98 , pp. 1803
    • Harata, K.1
  • 54
    • 0023713518 scopus 로고
    • Enantiomeric resolution and chiral recognition of racemic nicotine and nicotine analogues by β-cyclodextrins complexation. Structure-enantiomeric resolution relationship in host guest interaction
    • J. I. Seeman and H. V. Secor, Enantiomeric resolution and chiral recognition of racemic nicotine and nicotine analogues by β-cyclodextrins complexation. Structure-enantiomeric resolution relationship in host guest interaction, Anal. Chem. 60 (1988), 2120.
    • (1988) Anal. Chem. , vol.60 , pp. 2120
    • Seeman, J.I.1    Secor, H.V.2
  • 55
    • 0032937510 scopus 로고    scopus 로고
    • Reversed phase chromatographic study of the inclusion selectivity of terpene derivatives with β-cyclodextrines in water/cosolvent mixtures
    • A. K. Chatjigakis, I. Clarot, P. J. P. Cardot, R. Nowakowski, and A. Coleman, Reversed phase chromatographic study of the inclusion selectivity of terpene derivatives with β-cyclodextrines in water/cosolvent mixtures, J. Liq. Chrom Rel. Technol. 22 (1999), 1267.
    • (1999) J. Liq. Chrom Rel. Technol. , vol.22 , pp. 1267
    • Chatjigakis, A.K.1    Clarot, I.2    Cardot, P.J.P.3    Nowakowski, R.4    Coleman, A.5
  • 56
    • 0029891562 scopus 로고    scopus 로고
    • Determination of stochiometric coefficient and apparent formation constant for α- and β-CD complexes of terpenes using reversed phase liquid chromatography
    • C. Moeder, T. O'Brien, R. Thompson, and G. Bicker, Determination of stochiometric coefficient and apparent formation constant for α- and β-CD complexes of terpenes using reversed phase liquid chromatography, J. Chromatogr. 736 (1996), 1.
    • (1996) J. Chromatogr. , vol.736 , pp. 1
    • Moeder, C.1    O'Brien, T.2    Thompson, R.3    Bicker, G.4
  • 57
    • 0034672308 scopus 로고    scopus 로고
    • Chromatographic study of terpene derivatives on porous graphitic carbon stationary phase with β-cyclodextrin as mobile phase modifier
    • I. Clarot,D. Cledat, S. Battu, and P. J. P. Cardot, Chromatographic study of terpene derivatives on porous graphitic carbon stationary phase with β-cyclodextrin as mobile phase modifier, J. Chromatogr.A 903 (2000), 67.
    • (2000) J. Chromatogr.A , vol.903 , pp. 67
    • Clarot, I.1    Cledat, D.2    Battu, S.3    Cardot, P.J.P.4
  • 58
    • 0035022959 scopus 로고    scopus 로고
    • Fluorescence enhancement of coumarin-6-sulfonyl chloride amino acid derivatives in cyclodextrin media
    • S. M. Z. Al-Kindy, F. E. O. Sulman, and A. A. Al-Hamadi, Fluorescence enhancement of coumarin-6-sulfonyl chloride amino acid derivatives in cyclodextrin media, Anal. Sci. 17 (2001), 539.
    • (2001) Anal. Sci. , vol.17 , pp. 539
    • Al-Kindy, S.M.Z.1    Sulman, F.E.O.2    Al-Hamadi, A.A.3
  • 59
    • 0023902670 scopus 로고
    • Crystal structures of inclusion complexes of bcyclodextrin with (S)-(+)- and (R)-(-)-febpren
    • J. A. Hamilton and L. Chen, Crystal structures of inclusion complexes of bcyclodextrin with (S)-(+)- and (R)-(-)-febpren, J.Am.Chem. Soc. 110 (1988), 4379.
    • (1988) J.Am.Chem. Soc. , vol.110 , pp. 4379
    • Hamilton, J.A.1    Chen, L.2
  • 60
    • 22144474422 scopus 로고    scopus 로고
    • Selectivity of a native β- cyclodextrin column in the separation of catechins
    • A. Berthod, L. Berthod, and D. W. Armstrong, Selectivity of a native β- cyclodextrin column in the separation of catechins, J. Liq. Chrom Rel. Technol. 28 (2005), 1669.
    • (2005) J. Liq. Chrom Rel. Technol. , vol.28 , pp. 1669
    • Berthod, A.1    Berthod, L.2    Armstrong, D.W.3
  • 61
    • 0026065599 scopus 로고
    • Effect of the configuration of the substituents of derivatized β-cyclodextrin bonded phases on enantioselectivity in normal phase liquid chromatography
    • A. M. Stalcup, S.-C. Chang, and D.W. Armstrong, Effect of the configuration of the substituents of derivatized β-cyclodextrin bonded phases on enantioselectivity in normal phase liquid chromatography, J. Chromatogr. A. 540 (1991), 113.
    • (1991) J. Chromatogr. A. , vol.540 , pp. 113
    • Stalcup, A.M.1    Chang, S.-C.2    Armstrong, D.W.3
  • 63
    • 3042859718 scopus 로고
    • The discovery of crown ethers
    • Nobel Lecture
    • C. J. Pedersen, The discovery of crown ethers, Nobel Lecture, 1987.
    • (1987)
    • Pedersen, C.J.1
  • 64
    • 0041127939 scopus 로고
    • Cyclic polyethers and their complexes with metal salts
    • C. J. Pedersen, Cyclic polyethers and their complexes with metal salts, J. Am. Chem. Soc. 89 (1967), 7017.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 7017
    • Pedersen, C.J.1
  • 65
    • 0001050547 scopus 로고
    • Host-guest chemistry
    • D. J. Cram and J. M. Cram, Host-guest chemistry, Science 183 (1974), 803.
    • (1974) Science , vol.183 , pp. 803
    • Cram, D.J.1    Cram, J.M.2
  • 66
    • 33845558509 scopus 로고
    • Host-guest complexation. 23. High chiral recognition of amino acid and ester guests by hosts containing one chiral element
    • D. S. Lingenfelter, R. G. Helgeson, and D. J. Cram, Host-guest complexation. 23. High chiral recognition of amino acid and ester guests by hosts containing one chiral element, J. Org. Chem. 46 (1981), 393.
    • (1981) J. Org. Chem. , vol.46 , pp. 393
    • Lingenfelter, D.S.1    Helgeson, R.G.2    Cram, D.J.3
  • 68
    • 37049077036 scopus 로고
    • Source of chiral recognition in complexes with phenylglycine as guest
    • C. B. Knobler, F. C. A. Gaeta, and D. J. Cram, Source of chiral recognition in complexes with phenylglycine as guest, J. Chem. Soc. Chem. Commun. (1988), 330.
    • (1988) J. Chem. Soc. Chem. Commun. , pp. 330
    • Knobler, C.B.1    Gaeta, F.C.A.2    Cram, D.J.3
  • 69
    • 0040502386 scopus 로고
    • Chromatographic optical resolution through chiral complexation of amino ester salts by a host covalently bound to silica gel
    • G. Dotsevi,Y. Sogah, and D. J. Cram, Chromatographic optical resolution through chiral complexation of amino ester salts by a host covalently bound to silica gel, J. Am. Chem. Soc. 97 (1975), 1259.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 1259
    • Dotsevi, G.1    Sogah, Y.2    Cram, D.J.3
  • 70
    • 0343456237 scopus 로고
    • Host-guest complexation. 14. Host covalently bound to polystyrene resin for chromatographic resolution of enantiomers of amino acid and ester salts
    • G. Dotsevi, Y. Sogah, and D. J. Cram, Host-guest complexation. 14. Host covalently bound to polystyrene resin for chromatographic resolution of enantiomers of amino acid and ester salts, J. Am. Chem. Soc. 101 (1979), 3035.
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 3035
    • Dotsevi, G.1    Sogah, Y.2    Cram, D.J.3
  • 72
    • 0023658988 scopus 로고
    • Chromatographic separation of racemic amino acids by use of chiral crown ether-coated reversed-phase packings
    • T. Shimbo, T. Yamaguchi, K. Nishimura, and M. Sugiura, Chromatographic separation of racemic amino acids by use of chiral crown ether-coated reversed-phase packings, J. Chromatogr. 405 (1987), 145.
    • (1987) J. Chromatogr. , vol.405 , pp. 145
    • Shimbo, T.1    Yamaguchi, T.2    Nishimura, K.3    Sugiura, M.4
  • 73
    • 0014499213 scopus 로고
    • Solubilization of particulate proteins and nonelectrolytes by chaotropic agents
    • Y. Hatefi and W. G. Hanstein, Solubilization of particulate proteins and nonelectrolytes by chaotropic agents, Proc. Natl. Acad. Sci. USA 62 (1969), 1129.
    • (1969) Proc. Natl. Acad. Sci. USA , vol.62 , pp. 1129
    • Hatefi, Y.1    Hanstein, W.G.2
  • 74
    • 0029006278 scopus 로고
    • Mechanistic aspects of the stereospecific interaction for aminoindanol with crown ether column
    • R. A.Thompson, Z. Gee, N. Grinberg,D. Ellison, and P.Tway, Mechanistic aspects of the stereospecific interaction for aminoindanol with crown ether column, Anal. Chem. 67 (1995), 1580.
    • (1995) Anal. Chem. , vol.67 , pp. 1580
    • Thompson, R.A.1    Gee, Z.2    Grinberg, N.3    Ellison, D.4    Tway, P.5
  • 75
    • 0037283115 scopus 로고    scopus 로고
    • Enantiomeric separation of trans-2-aminocyclohexanol on a crown ether stationary phase using evaporative light scattering detection
    • S. Chen, H.Yuan, N. Grinberg, A. Dovletoglou, and G. Bicker, Enantiomeric separation of trans-2-aminocyclohexanol on a crown ether stationary phase using evaporative light scattering detection, J. Liq. Chromatogr. Rel.Technol. 25 (2003), 425.
    • (2003) J. Liq. Chromatogr. Rel.Technol. , vol.25 , pp. 425
    • Chen, S.1    Yuan, H.2    Grinberg, N.3    Dovletoglou, A.4    Bicker, G.5
  • 76
    • 0032566487 scopus 로고    scopus 로고
    • Liquid chromatographic resolution of racemic amino acids and their derivatives on a new chiral stationary phase based on crown ether
    • M. H. Hyun, J. S. Jin, and W. Lee, Liquid chromatographic resolution of racemic amino acids and their derivatives on a new chiral stationary phase based on crown ether, J. Chromatogr. 822 (1998), 155.
    • (1998) J. Chromatogr. , vol.822 , pp. 155
    • Hyun, M.H.1    Jin, J.S.2    Lee, W.3
  • 77
    • 0034741420 scopus 로고    scopus 로고
    • Chiral recognition of (18-crown- 6)tetracarboxylic acid as a chiral selector determined by NMR spectroscopy
    • E. Bang, J.-W. Jung,W. Lee,D.W. Lee, and W. Lee, Chiral recognition of (18-crown- 6)tetracarboxylic acid as a chiral selector determined by NMR spectroscopy, J. Chem. Soc. Perkin Trans II (2001), 1685.
    • (2001) J. Chem. Soc. Perkin Trans II , pp. 1685
    • Bang, E.1    Jung, J.-W.2    Lee, W.3    Lee, D.W.4    Lee, W.5
  • 78
    • 0035834298 scopus 로고    scopus 로고
    • Impact of triethylamine as mobile phase additive on the resolution of racemic amino acids on an (+)-18-crown-6-tetracarboxyllic acid derived stationary phase
    • J. S. Jin, A. M. Stalcup, and M. H. Hyun, Impact of triethylamine as mobile phase additive on the resolution of racemic amino acids on an (+)-18-crown-6-tetracarboxyllic acid derived stationary phase, J. Chromatogr.A 933 (2001), 83.
    • (2001) J. Chromatogr.A , vol.933 , pp. 83
    • Jin, J.S.1    Stalcup, A.M.2    Hyun, M.H.3
  • 79
    • 37049078268 scopus 로고
    • Theoretical models of charge-transfer complexes
    • C. J. Bender,Theoretical models of charge-transfer complexes, Chem. Soc. Rev. 15 (1986), 475.
    • (1986) Chem. Soc. Rev. , vol.15 , pp. 475
    • Bender, C.J.1
  • 80
    • 0036897848 scopus 로고    scopus 로고
    • Aromatic interactions in model systems
    • M. L.Waters, Aromatic interactions in model systems, Curr. Opin. Chem. Biol. 6 (2002), 736.
    • (2002) Curr. Opin. Chem. Biol. , vol.6 , pp. 736
    • Waters, M.L.1
  • 81
    • 0035200608 scopus 로고    scopus 로고
    • Attractive intermolecular edge-toface aromatic interactions in flexible organic molecules
    • W. B. Jennings, F. M. Farrell, and J. F. Malone, Attractive intermolecular edge-toface aromatic interactions in flexible organic molecules, Acc. Chem. Res. 34 (2001), 885.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 885
    • Jennings, W.B.1    Farrell, F.M.2    Malone, J.F.3
  • 82
    • 0024292833 scopus 로고
    • Aromatic rings act as hydrogen bond acceptor
    • M. Levitt and M. F. Perutz, Aromatic rings act as hydrogen bond acceptor, J. Mol. Biol. 201 (1988), 751.
    • (1988) J. Mol. Biol. , vol.201 , pp. 751
    • Levitt, M.1    Perutz, M.F.2
  • 83
    • 0003450560 scopus 로고
    • Organic Charge-Transfer Complexes
    • Academic Press, London
    • R. Foster, Organic Charge-Transfer Complexes, Academic Press, London, 1969, p. 182.
    • (1969) , pp. 182
    • Foster, R.1
  • 84
    • 0000877735 scopus 로고
    • A new reagent for resolution by complex formation; the resolution of phenanthro-[3,4-c]phenantrene
    • M. S. Newman, W. B. Lutz, and D. Lednicer, A new reagent for resolution by complex formation; the resolution of phenanthro-[3,4-c]phenantrene, J. Am. Chem. Soc. 77 (1955), 3420.
    • (1955) J. Am. Chem. Soc. , vol.77 , pp. 3420
    • Newman, M.S.1    Lutz, W.B.2    Lednicer, D.3
  • 85
    • 0344531805 scopus 로고
    • The synthesis and resolution of hexahelicene
    • M. S. Newman and D. Lednicer, The synthesis and resolution of hexahelicene, J. Am. Chem. Soc. 78 (1956), 4765.
    • (1956) J. Am. Chem. Soc. , vol.78 , pp. 4765
    • Newman, M.S.1    Lednicer, D.2
  • 86
    • 34547725624 scopus 로고
    • Optical resolution of 9-secbutylphenantrene by molecular complexation chromatography
    • L. H. Klemm, K. B. Desai, and J. J. R. Spooner, Optical resolution of 9-secbutylphenantrene by molecular complexation chromatography, J. Chromatogr. 14 (1964), 297.
    • (1964) J. Chromatogr. , vol.14 , pp. 297
    • Klemm, L.H.1    Desai, K.B.2    Spooner, J.J.R.3
  • 87
    • 0000844490 scopus 로고
    • Optical resolution by molecular complexation chromatography
    • L. H. Klemm and D. Reed, Optical resolution by molecular complexation chromatography, J. Chromatogr. 3 (1959), 364.
    • (1959) J. Chromatogr. , vol.3 , pp. 364
    • Klemm, L.H.1    Reed, D.2
  • 88
    • 0001681426 scopus 로고
    • Resolution of optical isomers by high performance liquid chromatography, Using coated and bonded chiral charge transfer complexing agents as stationary phase
    • F. Mikes, G. Boshart, and A. Gil-Av, Resolution of optical isomers by high performance liquid chromatography, using coated and bonded chiral charge transfer complexing agents as stationary phase, J. Chromatogr. 122 (1976), 205.
    • (1976) J. Chromatogr. , vol.122 , pp. 205
    • Mikes, F.1    Boshart, G.2    Gil-Av, A.3
  • 89
    • 2142728169 scopus 로고
    • The resolution of chiral compounds by modern liquid chromatography
    • Ph.D thesis, Organic Chemistry Department, The Weizmann Institute of Science, Rehovot, Israel
    • F. Mikes, The resolution of chiral compounds by modern liquid chromatography. Ph.D thesis, Organic Chemistry Department, 1975, The Weizmann Institute of Science, Rehovot, Israel.
    • (1975)
    • Mikes, F.1
  • 90
    • 0001585011 scopus 로고
    • The determination of optical purity by nuclear magnetic resonance
    • M. Raban and K. Mislow,The determination of optical purity by nuclear magnetic resonance, Tetrahedron Lett. 48 (1965), 4249.
    • (1965) Tetrahedron Lett. , vol.48 , pp. 4249
    • Raban, M.1    Mislow, K.2
  • 91
    • 0000925469 scopus 로고
    • The nonequivalence of physical properties of enantiomers in Optically active solvents. Differences in nuclear magnetic resonance spectra. I
    • W. H. Pirkle, The nonequivalence of physical properties of enantiomers in Optically active solvents. Differences in nuclear magnetic resonance spectra. I, J. Am. Chem. Soc. 88 (1966), 1837.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 1837
    • Pirkle, W.H.1
  • 92
    • 0001095817 scopus 로고
    • Resolution of optical isomers by liquid chromatography
    • W. H. Pirkle and D. L. Sikkenga, Resolution of optical isomers by liquid chromatography, J. Chromatogr. 123 (1976), 400.
    • (1976) J. Chromatogr. , vol.123 , pp. 400
    • Pirkle, W.H.1    Sikkenga, D.L.2
  • 93
    • 0018832870 scopus 로고
    • Broad spectrum resolution of optical isomers using chiral high-performance liquid chromatographic bonded phases
    • W. H. Pirkle, D.W. House, and J. M. Finn, Broad spectrum resolution of optical isomers using chiral high-performance liquid chromatographic bonded phases, J. Chromatogr. 192 (1980), 143.
    • (1980) J. Chromatogr. , vol.192 , pp. 143
    • Pirkle, W.H.1    House, D.W.2    Finn, J.M.3
  • 94
    • 0011265223 scopus 로고
    • Separation of enantiomers by liquid chromatographic methods
    • in J.D. Norrison (ed.), Analytical Methods, Academic Press, New York
    • W. H. Pirkle and J. Finn, Separation of enantiomers by liquid chromatographic methods, in J.D. Norrison (ed.), Asymmetric Synthesis,Vol. 1. Analytical Methods, Academic Press, New York, 1983, p. 87.
    • (1983) Asymmetric Synthesis , vol.1 , pp. 87
    • Pirkle, W.H.1    Finn, J.2
  • 95
    • 0027287673 scopus 로고
    • Chiral stationary phase design. Use of intercalative effects to enhance enantioselectivity
    • W. H. Pirkle and P. G. Murray, Chiral stationary phase design. Use of intercalative effects to enhance enantioselectivity, J. Chromatogr. 641 (1993), 11.
    • (1993) J. Chromatogr. , vol.641 , pp. 11
    • Pirkle, W.H.1    Murray, P.G.2
  • 96
    • 0000903758 scopus 로고    scopus 로고
    • X-ray crystallographic evidence support of a proposed chiral recognition mechanism
    • W. H. Pirkle, P. G. Murray, and S. R. Wilson, X-ray crystallographic evidence support of a proposed chiral recognition mechanism, J. Org. Chem. 61 (1996), 4775.
    • (1996) J. Org. Chem. , vol.61 , pp. 4775
    • Pirkle, W.H.1    Murray, P.G.2    Wilson, S.R.3
  • 97
    • 0026720612 scopus 로고
    • Designed, Synthesis and evaluation of an improved enantioselective naproxen selector
    • W. H. Pirkle, C. J.Welch, and B. Lamm, Designed, synthesis and evaluation of an improved enantioselective naproxen selector, J. Org. Chem. 57 (1992), 3854.
    • (1992) J. Org. Chem. , vol.57 , pp. 3854
    • Pirkle, W.H.1    Welch, C.J.2    Lamm, B.3
  • 98
    • 0028284222 scopus 로고
    • Use of simultaneous face to face and face to edge π-π interactions to facilitate chiral recognition
    • W. H. Pirkle and C. J.Welch, Use of simultaneous face to face and face to edge π-π interactions to facilitate chiral recognition, Tetrahedron Asymmetry 5 (1994), 777.
    • (1994) Tetrahedron Asymmetry , vol.5 , pp. 777
    • Pirkle, W.H.1    Welch, C.J.2
  • 99
    • 33751155167 scopus 로고
    • Chiral recognition studies: Intra- and intermolecular 1H{1H}-nuclear Overhauser effects as effective tools in the study of bimolecular complexes
    • W. H. Pirkle and S. R. Selness, Chiral recognition studies: Intra- and intermolecular 1H{1H}-nuclear Overhauser effects as effective tools in the study of bimolecular complexes, J. Org. Chem. 60 (1995), 3252.
    • (1995) J. Org. Chem. , vol.60 , pp. 3252
    • Pirkle, W.H.1    Selness, S.R.2
  • 100
    • 0025863823 scopus 로고
    • Chiral stationary phase derived from tyrosine
    • M. Caude, A. Tambute, and L. Siret, Chiral stationary phase derived from tyrosine, J. Chromatogr. 550 (1991), 357.
    • (1991) J. Chromatogr. , vol.550 , pp. 357
    • Caude, M.1    Tambute, A.2    Siret, L.3
  • 101
    • 0030576524 scopus 로고
    • Quinince and quinidine derivatives as chiral selectors. Beush type chiral stationary phases for high performance liquid chromatography based on chincona carbamates and their applications as chiral anion exchanger
    • M. Lammerhofer and W. Lindner, Quinince and quinidine derivatives as chiral selectors. Beush type chiral stationary phases for high performance liquid chromatography based on chincona carbamates and their applications as chiral anion exchanger, J. Chromatogr. 741 (1966), 33.
    • (1966) J. Chromatogr. , vol.741 , pp. 33
    • Lammerhofer, M.1    Lindner, W.2
  • 102
    • 0033962554 scopus 로고    scopus 로고
    • Enantiomeric discrimination by a quinine-based chiral stationary phase: A computational study
    • S. Schefzig,W. Lindner, K. B. Lipkowitz, and M. Jalaie, Enantiomeric discrimination by a quinine-based chiral stationary phase: A computational study, Chirality 12 (2000), 7.
    • (2000) Chirality , vol.12 , pp. 7
    • Schefzig, S.1    Lindner, W.2    Lipkowitz, K.B.3    Jalaie, M.4
  • 103
    • 0003954817 scopus 로고    scopus 로고
    • Organic Chemistry
    • McGraw-Hill, New York
    • F. A. Carey, Organic Chemistry, McGraw-Hill, New York, 1996, p. 1034.
    • (1996) , pp. 1034
    • Carey, F.A.1
  • 104
    • 0004110428 scopus 로고
    • Principles of biochemistry
    • Worth Publishers, New York
    • A. L. Lehninger, Principles of biochemistry, Worth Publishers, New York, 1982, p. 277.
    • (1982) , pp. 277
    • Lehninger, A.L.1
  • 105
    • 0025315905 scopus 로고
    • Adsorption chromatography. VI. Further studies on the separation of d- and l-tryprophan on cellulose with aqueous solvents
    • M. Lederer, Adsorption chromatography. VI. Further studies on the separation of d- and l-tryprophan on cellulose with aqueous solvents, J. Chromatogr. A. 510 (1990), 367.
    • (1990) J. Chromatogr. A. , vol.510 , pp. 367
    • Lederer, M.1
  • 106
    • 0026749363 scopus 로고
    • Adsorption chromatography. VII. Chiral separation on cellulose with aqueous solvents
    • M. Lederer, Adsorption chromatography. VII. Chiral separation on cellulose with aqueous solvents, J. Chromatogr.A. 604 (1992), 55.
    • (1992) J. Chromatogr.A. , vol.604 , pp. 55
    • Lederer, M.1
  • 107
    • 0027411833 scopus 로고
    • Adsorption chromatography. IX. Chiral separation with aqueous solvents and liquid-liquid systems
    • H.T. K. Xuan and M. Lederer, Adsorption chromatography. IX. Chiral separation with aqueous solvents and liquid-liquid systems, J. Chromatogr. A. 635 (1993), 346.
    • (1993) J. Chromatogr. A. , vol.635 , pp. 346
    • Xuan, H.T.K.1    Lederer, M.2
  • 108
    • 0002127595 scopus 로고
    • Polysaccharide phases
    • in A. M. Krstulovic (ed.), Chiral Separation by HPLC. Applications to Pharmaceutical Compounds, Ellis Horwood, New York
    • T. Shibata, K. Mori, and Y. Okamoto, Polysaccharide phases, in A. M. Krstulovic (ed.), Chiral Separation by HPLC. Applications to Pharmaceutical Compounds, Ellis Horwood, New York, 1989, P. 336.
    • (1989) , pp. 336
    • Shibata, T.1    Mori, K.2    Okamoto, Y.3
  • 109
    • 0015800169 scopus 로고
    • Eine volstandige Racemattrennung durch Elutions- Chromatographie an Cellulose-tri-acetat
    • G. Hesse and R. Hagel, Eine volstandige Racemattrennung durch Elutions- Chromatographie an Cellulose-tri-acetat, Chromatographia 6 (1973), 277.
    • (1973) Chromatographia , vol.6 , pp. 277
    • Hesse, G.1    Hagel, R.2
  • 110
    • 0002784362 scopus 로고
    • Band broadening in high-performance liquid chromatographic separations of enantiomers with swollen microcystalline cellulose triacetate packings. I. Influence of capacity factor, Analyte structure, flow velocity and column loading
    • A. M. Rizzi, Band broadening in high-performance liquid chromatographic separations of enantiomers with swollen microcystalline cellulose triacetate packings. I. Influence of capacity factor, analyte structure, flow velocity and column loading, J. Chromatogr.A. 478 (1989), 71.
    • (1989) J. Chromatogr.A. , vol.478 , pp. 71
    • Rizzi, A.M.1
  • 111
    • 0006598577 scopus 로고
    • Chromatographic chiral resolution. XIV. Cellulose tribenzoate derivatives as chiral stationary phases for high performance liquid chromatography
    • Y. Okamoto, R. Aburatini, and K. Hatada, Chromatographic chiral resolution. XIV. Cellulose tribenzoate derivatives as chiral stationary phases for high performance liquid chromatography, J. Chromatogr.A 389 (1987), 95.
    • (1987) J. Chromatogr.A , vol.389 , pp. 95
    • Okamoto, Y.1    Aburatini, R.2    Hatada, K.3
  • 112
    • 0001990012 scopus 로고
    • Homogeneous and heterogeneous cellulos triester and a cellulose triurethane: synthesis and structural investigation of the crystaline state
    • H. Steinmeier, P. Zugenmaier, Homogeneous and heterogeneous cellulos triester and a cellulose triurethane: synthesis and structural investigation of the crystaline state. Carbohydr. Res. 164 (1987), 97.
    • (1987) Carbohydr. Res. , vol.164 , pp. 97
    • Steinmeier, H.1    Zugenmaier, P.2
  • 114
    • 0032482102 scopus 로고    scopus 로고
    • Polysaccharide derivatives for chromatographic separation of enantiomers
    • Y. Okamoto and E.Yashima, Polysaccharide derivatives for chromatographic separation of enantiomers, Angew. Chem. Int. Ed. 37 (1998), 1020.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1020
    • Okamoto, Y.1    Yashima, E.2
  • 115
    • 0034672766 scopus 로고    scopus 로고
    • Enantiomeric separation of some pharmaceutical intermediates and reversal of elution order by high performance liquid chromatography using cellulose and amylose tris-3,5-demethylphenylcarbamate) derivatives as stationary phase
    • T.Wang, Y.W. Chen, and A. Vailaya, Enantiomeric separation of some pharmaceutical intermediates and reversal of elution order by high performance liquid chromatography using cellulose and amylose tris-3,5-demethylphenylcarbamate) derivatives as stationary phase, J. Chromatogr.A 902 (2000), 345.
    • (2000) J. Chromatogr.A , vol.902 , pp. 345
    • Wang, T.1    Chen, Y.W.2    Vailaya, A.3
  • 116
    • 33644812832 scopus 로고    scopus 로고
    • The use of polysaccharide phases in the separation of enantiomers
    • in E. Grushka and N. Grinberg (eds.), Advances in Chromatography, Taylor & Francis, Boca Raton, FL
    • R. W. Stringham, The use of polysaccharide phases in the separation of enantiomers, in E. Grushka and N. Grinberg (eds.), Advances in Chromatography, Taylor & Francis, Boca Raton, FL, 2006, p. 257.
    • (2006) , pp. 257
    • Stringham, R.W.1
  • 117
    • 0034885143 scopus 로고    scopus 로고
    • Vancomycin, teicoplanin and ramoplanin: Synthetic and mechanistic studies
    • D. L. Boger,Vancomycin, teicoplanin and ramoplanin: Synthetic and mechanistic studies, Med. Res. Rev. 21 (2001), 356.
    • (2001) Med. Res. Rev. , vol.21 , pp. 356
    • Boger, D.L.1
  • 118
    • 0031828171 scopus 로고    scopus 로고
    • High enantioselective HPLC separations using the covalent bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase
    • K. H. Ekborg-Ott, L.Youbang, and D.W.Armstrong, High enantioselective HPLC separations using the covalent bonded macrocyclic antibiotic, ristocetin A, chiral stationary phase. Chirality, 10 (1998), 434.
    • (1998) Chirality , vol.10 , pp. 434
    • Ekborg-Ott, K.H.1    Youbang, L.2    Armstrong, D.W.3
  • 119
    • 0021154432 scopus 로고
    • The structure and mode of action of glycopeptide antibiotics of the vancomycin group
    • J. C. J. Barna and D. H.Williams, The structure and mode of action of glycopeptide antibiotics of the vancomycin group, Annu. Rev. Microbiol. 38 (1984), 339.
    • (1984) Annu. Rev. Microbiol. , vol.38 , pp. 339
    • Barna, J.C.J.1    Williams, D.H.2
  • 120
    • 0033880691 scopus 로고    scopus 로고
    • The structural biology of molecular recognition by vancomycin
    • P. J. Loll and P. H. Axelsen, The structural biology of molecular recognition by vancomycin, Annu. Rev. Biophys. Biomol. Struct. 29 (2000), 265.
    • (2000) Annu. Rev. Biophys. Biomol. Struct. , vol.29 , pp. 265
    • Loll, P.J.1    Axelsen, P.H.2
  • 121
    • 0017802490 scopus 로고
    • Structure of vancomycin and its complex with acetyl-d-alanyl-d-alanine
    • G. M. Sheldrick, P. G. Jones, O. Kennard, D. H.Williams, G. A. Smith, Structure of vancomycin and its complex with acetyl-d-alanyl-d-alanine, Nature 271 (1978), 223.
    • (1978) Nature , vol.271 , pp. 223
    • Sheldrick, G.M.1    Jones, P.G.2    Kennard, O.3    Williams, D.H.4    Smith, G.A.5
  • 122
    • 0016605724 scopus 로고
    • A nuclear magnetic resonance study of the interaction between cancomycin and actyl-d-alanyl-d-alanine in aqueous solution
    • J. P. Brown, J. Feeney, and A. S.V. Burgen, A nuclear magnetic resonance study of the interaction between cancomycin and actyl-d-alanyl-d-alanine in aqueous solution, Mol. Pharmacol. 11 (1975), 119.
    • (1975) Mol. Pharmacol. , vol.11 , pp. 119
    • Brown, J.P.1    Feeney, J.2    Burgen, A.S.V.3
  • 123
    • 0016605725 scopus 로고
    • A structure-activity study by nuclear magnetic resonance of peptide interactions with vancomycin
    • J. P. Brown, L. Terenius, J. Feeney, and A. S.V. Burgen, A structure-activity study by nuclear magnetic resonance of peptide interactions with vancomycin. Mol. Pharmacol. 11 (1975), 126.
    • (1975) Mol. Pharmacol. , vol.11 , pp. 126
    • Brown, J.P.1    Terenius, L.2    Feeney, J.3    Burgen, A.S.V.4
  • 124
    • 0015102039 scopus 로고
    • Modifications of the acyl-d-alanyl-d-alanine terminus affecting complex formation with vancomycin
    • M. Nieto and H. R. Perkins, Modifications of the acyl-d-alanyl-d-alanine terminus affecting complex formation with vancomycin, Biochem. J. 123 (1971), 789.
    • (1971) Biochem. J. , vol.123 , pp. 789
    • Nieto, M.1    Perkins, H.R.2
  • 125
    • 0014446989 scopus 로고
    • Specificity of combination between mucopeptide precursors and vancomycin or ristocetin
    • H. R. Perkins, Specificity of combination between mucopeptide precursors and vancomycin or ristocetin, Biochem. J. 111 (1969), 195.
    • (1969) Biochem. J. , vol.111 , pp. 195
    • Perkins, H.R.1
  • 126
    • 0028227322 scopus 로고
    • Macrocyclic antibiotics as a new class of chiral selectors for liquid chromatography
    • D.W. Armstrong, Y. Tang, S. Chen, Y. Zhou, C. Bagwill, and J.-R. Chen, Macrocyclic antibiotics as a new class of chiral selectors for liquid chromatography, Anal. Chem. 66 (1994), 1473.
    • (1994) Anal. Chem. , vol.66 , pp. 1473
    • Armstrong, D.W.1    Tang, Y.2    Chen, S.3    Zhou, Y.4    Bagwill, C.5    Chen, J.-R.6
  • 127
    • 1342286885 scopus 로고    scopus 로고
    • Study of mechanism of chiral discrimination of amino acids and their derivatives on a teicoplanin-based chiral stationary phase
    • A. Cavazzini, G. Nadalini, F. Dondi, F. Gasparini, A. Ciogli, and C. Villani, Study of mechanism of chiral discrimination of amino acids and their derivatives on a teicoplanin-based chiral stationary phase, J. Chromatogr.A 1031 (2004), 143.
    • (2004) J. Chromatogr.A , vol.1031 , pp. 143
    • Cavazzini, A.1    Nadalini, G.2    Dondi, F.3    Gasparini, F.4    Ciogli, A.5    Villani, C.6
  • 128
    • 0033305976 scopus 로고    scopus 로고
    • Effect of selector coverage and mobile phase composition on enantiomeric separation with ristocetin A chiral stationary phase
    • K. H. Ekborg-Ott, X.Wang, and D.W. Armstrong, Effect of selector coverage and mobile phase composition on enantiomeric separation with ristocetin A chiral stationary phase, Microchem. J. 62 (1999), 26.
    • (1999) Microchem. J. , vol.62 , pp. 26
    • Ekborg-Ott, K.H.1    Wang, X.2    Armstrong, D.W.3
  • 129
    • 0038518887 scopus 로고    scopus 로고
    • Enantioseparation of semisynthetic ergot alkaloids on vancomycin and teicoplanin stationary phases
    • E.Tesarova, K. Zaruba, and M. Flieger, Enantioseparation of semisynthetic ergot alkaloids on vancomycin and teicoplanin stationary phases, J. Chromatogr.A 844 (1999), 137.
    • (1999) J. Chromatogr.A , vol.844 , pp. 137
    • Tesarova, E.1    Zaruba, K.2    Flieger, M.3
  • 130
    • 0004110428 scopus 로고
    • Principles of biochemistry
    • Worth Publisher, New York
    • A. L. Lehninger, Principles of biochemistry, Worth Publisher, New York, 1982, p. 121.
    • (1982) , pp. 121
    • Lehninger, A.L.1
  • 131
    • 0004140795 scopus 로고
    • Proteins Structure and Molecular Properties
    • W.H. Freeman, New York
    • T. E. Creighton, Proteins Structure and Molecular Properties, W.H. Freeman, New York, 1993, p. 182.
    • (1993) , pp. 182
    • Creighton, T.E.1
  • 132
    • 0004122938 scopus 로고
    • Biochemistry
    • Addison-Wesley, Reading, MA
    • G. Zubay, Biochemistry, Addison-Wesley, Reading, MA, 1983, p. 8.
    • (1983) , pp. 8
    • Zubay, G.1
  • 133
    • 0030474049 scopus 로고    scopus 로고
    • What can we learn from molecular recognition in protein-ligand complexes for the design of new drugs
    • H. J. Bohm and G. Klebe, What can we learn from molecular recognition in protein-ligand complexes for the design of new drugs? Angew. Chem. Int. Ed. 35 (1996), 2589.
    • (1996) Angew. Chem. Int. Ed. , vol.35 , pp. 2589
    • Bohm, H.J.1    Klebe, G.2
  • 134
    • 0004002507 scopus 로고    scopus 로고
    • Physical Chemistry of Surfaces
    • John Wiley & Sons, New York
    • A.W.Adamson and A. P. Gast, Physical Chemistry of Surfaces, John Wiley & Sons, New York, 1997, p. 246.
    • (1997) , pp. 246
    • Adamson, A.W.1    Gast, A.P.2
  • 135
    • 24744465619 scopus 로고    scopus 로고
    • A systematic analysis of the effect of smallmolecule binding on protein flexibility of the ligand binding sites
    • C. Y. Yang, R. Wang, and S. Wang, A systematic analysis of the effect of smallmolecule binding on protein flexibility of the ligand binding sites, J. Med. Chem. 48 (2005), 5648.
    • (2005) J. Med. Chem. , vol.48 , pp. 5648
    • Yang, C.Y.1    Wang, R.2    Wang, S.3
  • 136
    • 0035353104 scopus 로고    scopus 로고
    • Liquid chromatographic studies of the effect of phosphate on the binding properties of silica-immobilized bovine serum albumin
    • W. A.Tao and R. K. Gilpin, Liquid chromatographic studies of the effect of phosphate on the binding properties of silica-immobilized bovine serum albumin, J. Chromatogr. Sci. 39 (2001), 205.
    • (2001) J. Chromatogr. Sci. , vol.39 , pp. 205
    • Tao, W.A.1    Gilpin, R.K.2
  • 137
    • 0036107851 scopus 로고    scopus 로고
    • Towards a general model for protein-substrate stereoselectivity
    • V. Sundaresan and R.Abrol,Towards a general model for protein-substrate stereoselectivity, Protein Sci. 11 (2002), 1330.
    • (2002) Protein Sci. , vol.11 , pp. 1330
    • Sundaresan, V.1    Abrol, R.2
  • 138
    • 0026704392 scopus 로고
    • Immobilized proteins as chromatographic supports for chiral resolution
    • S. R. Narayanan, Immobilized proteins as chromatographic supports for chiral resolution, J. Pharm. Biol. Anal. 10 (1992), 251.
    • (1992) J. Pharm. Biol. Anal. , vol.10 , pp. 251
    • Narayanan, S.R.1
  • 139
    • 0023056349 scopus 로고
    • Direct analytical and preparative resolution of enantiomers using albumin adsorbed to silica as a stationary phase
    • P. Erlandsson, L. Hansson, and R. Isaksson, Direct analytical and preparative resolution of enantiomers using albumin adsorbed to silica as a stationary phase, J. Chromatogr. 370 (1986), 475.
    • (1986) J. Chromatogr. , vol.370 , pp. 475
    • Erlandsson, P.1    Hansson, L.2    Isaksson, R.3
  • 140
    • 0035847245 scopus 로고    scopus 로고
    • Protein-based chiral stationary phases for high performance liquid chromatography enantioseparations
    • J. Haginaka, Protein-based chiral stationary phases for high performance liquid chromatography enantioseparations, J. Chromatogr.A 906 (2001), 253.
    • (2001) J. Chromatogr.A , vol.906 , pp. 253
    • Haginaka, J.1
  • 142
    • 0032899125 scopus 로고    scopus 로고
    • Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein. V. Influence of immobilization method on chiral separation
    • J. Haginaka,Y. Okazaki, and H. Matsunaga, Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein. V. Influence of immobilization method on chiral separation, J. Chromatogr. 840 (1999), 171.
    • (1999) J. Chromatogr. , vol.840 , pp. 171
    • Haginaka, J.1    Okazaki, Y.2    Matsunaga, H.3
  • 143
    • 0030914443 scopus 로고    scopus 로고
    • Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein. I. Influence of the pore size of base silica materials and bound protein amounts on chiral resolution
    • J. Haginaka and H. Takehira, Separation of enantiomers on a chiral stationary phase based on ovoglycoprotein. I. Influence of the pore size of base silica materials and bound protein amounts on chiral resolution, J. Chromatogr. 773 (1997), 85.
    • (1997) J. Chromatogr. , vol.773 , pp. 85
    • Haginaka, J.1    Takehira, H.2
  • 145
    • 0031928527 scopus 로고    scopus 로고
    • Unexpected difference in enantioselectivie retention on cellulase (CBH I) silica stationary phase caused by exchange of potassium for sodium in the mobile phase
    • M. Hedeland, S. Jonsson, R. Isaksson, and C. Petterson, Unexpected difference in enantioselectivie retention on cellulase (CBH I) silica stationary phase caused by exchange of potassium for sodium in the mobile phase, Chirality 10 (1998), 513.
    • (1998) Chirality , vol.10 , pp. 513
    • Hedeland, M.1    Jonsson, S.2    Isaksson, R.3    Petterson, C.4
  • 146
    • 0001419613 scopus 로고
    • Liquid chromatographic studies of the effect of temperature on the chiral recognition of tryptophan by silicaimmobilized bovine albumine
    • R. K. Gilpin, S. E. Ethesham, and R. B. Gregory, Liquid chromatographic studies of the effect of temperature on the chiral recognition of tryptophan by silicaimmobilized bovine albumine, Anal. Chem. 63 (1991), 2825.
    • (1991) Anal. Chem. , vol.63 , pp. 2825
    • Gilpin, R.K.1    Ethesham, S.E.2    Gregory, R.B.3
  • 147
    • 0007310356 scopus 로고
    • Ligand exchange chromatography of chiral compounds
    • in D. Cagniant (ed.), Marcel Dekker, New York
    • V. A. Davankov, Ligand exchange chromatography of chiral compounds, in D. Cagniant (ed.), Complexation Chromatography, Marcel Dekker, New York, 1992, p. 197.
    • (1992) Complexation Chromatography , pp. 197
    • Davankov, V.A.1
  • 148
    • 0001363568 scopus 로고
    • Ligand exchange: A novel separation technique
    • F. Helfferich, Ligand exchange: A novel separation technique, Nature 189 (1961), 1001.
    • (1961) Nature , vol.189 , pp. 1001
    • Helfferich, F.1
  • 149
    • 37049126956 scopus 로고
    • Ligand chromatography on asymmetric complex-forming sorbent as a new method for resolution of racemates
    • S. V. Rogozhin and V. A. Davankov, Ligand chromatography on asymmetric complex-forming sorbent as a new method for resolution of racemates, Chem. Commun. (1971), 490.
    • (1971) Chem. Commun. , pp. 490
    • Rogozhin, S.V.1    Davankov, V.A.2
  • 150
    • 0028216029 scopus 로고
    • Chiral selectors with chelating properties in liquid chromatography: Fundamental reflections and selective review of recent development
    • V. A. Davankov, Chiral selectors with chelating properties in liquid chromatography: Fundamental reflections and selective review of recent development, J. Chromatogr.A 666 (1994), 55.
    • (1994) J. Chromatogr.A , vol.666 , pp. 55
    • Davankov, V.A.1
  • 151
    • 0001166992 scopus 로고
    • Effect of the hydrophobic spacer in bonded [Cu(l-hydroxyprolyl)alkyl]+ silicas on retention and enantioselectivity and enantioselectivity of α-amino acids in high performance liquid chromatography
    • P. Roumeliotis, A. A. Kurganov, and V. A. Davankov, Effect of the hydrophobic spacer in bonded [Cu(l-hydroxyprolyl)alkyl]+ silicas on retention and enantioselectivity and enantioselectivity of α-amino acids in high performance liquid chromatography. J. Chromatogr.A 266 (1983), 439.
    • (1983) J. Chromatogr.A , vol.266 , pp. 439
    • Roumeliotis, P.1    Kurganov, A.A.2    Davankov, V.A.3
  • 152
    • 0026028314 scopus 로고
    • Efficiency in chiral high performance ligand exchange chromatography. Influence of complexation process, flow rate and capacity factor
    • A. M. Rizzi, Efficiency in chiral high performance ligand exchange chromatography. Influence of complexation process, flow rate and capacity factor, J. Chromatogr. A 542 (1991), 221.
    • (1991) J. Chromatogr. A , vol.542 , pp. 221
    • Rizzi, A.M.1
  • 153
    • 1842265389 scopus 로고
    • Ternary complexation
    • in A. M. Krstulovic (ed.), Chiral Separation by HPLC, Ellis Horwood, New York
    • N. Nimura, Ternary complexation, in A. M. Krstulovic (ed.), Chiral Separation by HPLC, Ellis Horwood, New York, 1993, p. 107.
    • (1993) , pp. 107
    • Nimura, N.1
  • 154
    • 0035408563 scopus 로고    scopus 로고
    • Thin-layer chromatography- A useful technique for the separation of enantiomers
    • Y. Bereznitski, R. Thompson, E. O'Neill, and N. Grinberg, Thin-layer chromatography- A useful technique for the separation of enantiomers, J. AOAC Int. 84 (2001), 1242.
    • (2001) J. AOAC Int. , vol.84 , pp. 1242
    • Bereznitski, Y.1    Thompson, R.2    O'Neill, E.3    Grinberg, N.4
  • 155
    • 0003598273 scopus 로고
    • Chiral separation in thin-layer chromatography
    • in N. Grinberg (ed.), Marcel Dekker, New York
    • N. Grinberg, Chiral separation in thin-layer chromatography, in N. Grinberg (ed.), Modern Thin-Layer Chromatography, Marcel Dekker, New York, 1990, pp. 398-402.
    • (1990) Modern Thin-Layer Chromatography , pp. 398-402
    • Grinberg, N.1
  • 156
    • 0023795601 scopus 로고
    • Thin layer chromatographic resolution via ligand exchange
    • K. Gunter, Thin layer chromatographic resolution via ligand exchange, J. Chromatogr. 448 (1988), 11.
    • (1988) J. Chromatogr. , vol.448 , pp. 11
    • Gunter, K.1
  • 157
    • 0029891562 scopus 로고    scopus 로고
    • Determination of stochiometric coefficient and apparent formation constant for α- and β-CD complexes of terpenes using reversed-phase liquid chromatography
    • C. Moeder, T. O'Brien, R. Thompson, and G. Bicker, Determination of stochiometric coefficient and apparent formation constant for α- and β-CD complexes of terpenes using reversed-phase liquid chromatography, J. Chromatogr. 1-2 (1996), 1.
    • (1996) J. Chromatogr , vol.1 , Issue.2 , pp. 1
    • Moeder, C.1    O'Brien, T.2    Thompson, R.3    Bicker, G.4
  • 158
    • 0027165511 scopus 로고
    • Chiral stationary phases in concert with homologous chiral mobile phases additives: Push/pull model
    • K. J. Duff, H. L. Gray, R. J. Gray, and C. C. Bahler, Chiral stationary phases in concert with homologous chiral mobile phases additives: Push/pull model, Chirality 5 (1993), 201
    • (1993) Chirality , vol.5 , pp. 201
    • Duff, K.J.1    Gray, H.L.2    Gray, R.J.3    Bahler, C.C.4
  • 159
    • 85052169403 scopus 로고
    • Separation of enantiomers
    • in V. A. Davankov, J. D. Navratil, and H. F.Walton, (eds.), CRC Press, Boca Raton, FL
    • V. A. Davankov, Separation of enantiomers, in V. A. Davankov, J. D. Navratil, and H. F.Walton, (eds.), Ligand Exchange Chromatography, CRC Press, Boca Raton, FL, 1988, p. 67.
    • (1988) Ligand Exchange Chromatography , pp. 67
    • Davankov, V.A.1
  • 160
    • 0012049198 scopus 로고
    • Resolution of underivatized amino acids by reversed phase chromatography
    • E. Gil-Av, A.Tishbee, and P. E. Hare, Resolution of underivatized amino acids by reversed phase chromatography, J. Am. Chem. Soc. 102 (1980), 5115.
    • (1980) J. Am. Chem. Soc. , vol.102 , pp. 5115
    • Gil-Av, E.1    Tishbee, A.2    Hare, P.E.3
  • 161
    • 0023348662 scopus 로고
    • Proposal for the classification of high performance liquid chromatographic stationary phases: How to choose the right column
    • I. W. Wainer, Proposal for the classification of high performance liquid chromatographic stationary phases: How to choose the right column, TRAC 6 (1987), 125.
    • (1987) TRAC , vol.6 , pp. 125
    • Wainer, I.W.1
  • 162
    • 0029867734 scopus 로고    scopus 로고
    • Use of subcritical fluid chromatography for the separation of enantiomers using packed column cellulose based stationary phase
    • T. Loughlin, R. Thompson, G. Bicker, P. Tway, and N. Grinberg, Use of subcritical fluid chromatography for the separation of enantiomers using packed column cellulose based stationary phase, Chirality 8 (1996), 157.
    • (1996) Chirality , vol.8 , pp. 157
    • Loughlin, T.1    Thompson, R.2    Bicker, G.3    Tway, P.4    Grinberg, N.5
  • 163
    • 0002130889 scopus 로고
    • Drug stereochemistry
    • in I.W.Wainer (ed.), 2nd edition, Marcel Dekker, New York
    • I.W.Wainer, Drug stereochemistry, in I.W.Wainer (ed.), Analytical Methods and Pharmacology, 2nd edition, Marcel Dekker, New York, 1993, p. 139.
    • (1993) Analytical Methods and Pharmacology , pp. 139
    • Wainer, I.W.1
  • 164
    • 84889300457 scopus 로고    scopus 로고
    • Chiral separation methods
    • in S. Ahuja (ed.), Chiral Separation, Applications and Technologies, American Chemical Society, Washington D.C
    • S. Ahuja, Chiral separation methods, in S. Ahuja (ed.), Chiral Separation, Applications and Technologies, American Chemical Society, Washington D.C., 1997, p. 138.
    • (1997) , pp. 138
    • Ahuja, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.