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Volumn 5, Issue , 2015, Pages

Engineering Cyclodextrin Clicked Chiral Stationary Phase for High-Efficiency Enantiomer Separation

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EID: 84938633118     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep11523     Document Type: Article
Times cited : (36)

References (35)
  • 1
    • 84904656053 scopus 로고    scopus 로고
    • Engineering chiral porous metal-organic frameworks for enantioselective adsorption and separation
    • Peng, Y. et al. Engineering chiral porous metal-organic frameworks for enantioselective adsorption and separation. Nat. Commun. 5, doi: 10.1038/ncomms5406 (2014).
    • (2014) Nat. Commun. , vol.5
    • Peng, Y.1
  • 4
    • 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. 89, 347-362 (1989).
    • (1989) Chem. Rev. , vol.89 , pp. 347-362
    • Pirkle, W.H.1    Pochapsky, T.C.2
  • 5
    • 84863222291 scopus 로고    scopus 로고
    • Recent advances in pharmaceutical separations with supercritical fluid chromatography and chiral columns
    • Wang, R., Ong, T. T., Tang, W. & Ng, S. C. Recent advances in pharmaceutical separations with supercritical fluid chromatography and chiral columns. TrAC-Trends Anal. Chem. 37, 83-100 (2012).
    • (2012) TrAC-Trends Anal. Chem. , vol.37 , pp. 83-100
    • Wang, R.1    Ong, T.T.2    Tang, W.3    Ng, S.C.4
  • 6
    • 84919809231 scopus 로고    scopus 로고
    • Recent development of cationic cyclodextrins for chiral separation
    • Zhou, J., Tang, J. & Tang, W. Recent development of cationic cyclodextrins for chiral separation. TrAC-Trends Anal. Chem. 65, 22-29 (2015).
    • (2015) TrAC-Trends Anal. Chem. , vol.65 , pp. 22-29
    • Zhou, J.1    Tang, J.2    Tang, W.3
  • 7
    • 11644249583 scopus 로고
    • Cyclodextrins and their applications in analytical chemistry
    • Li, S. & Purdy, W. C. Cyclodextrins and their applications in analytical chemistry. Chem. Rev. 92, 1457-1470 (1992).
    • (1992) Chem. Rev. , vol.92 , pp. 1457-1470
    • Li, S.1    Purdy, W.C.2
  • 8
    • 0028227322 scopus 로고
    • Macrocyclic antibiotics as a new class of chiral selectors for liquid chromatography
    • Armstrong, D. W. et al. Macrocyclic antibiotics as a new class of chiral selectors for liquid chromatography. Anal. Chem. 66, 1473-1484 (1994).
    • (1994) Anal. Chem. , vol.66 , pp. 1473-1484
    • Armstrong, D.W.1
  • 9
    • 0038777333 scopus 로고    scopus 로고
    • Enantioselective ligand exchange in modern separation techniques
    • Davankov, V. A. Enantioselective ligand exchange in modern separation techniques. J. Chromatogr. A 1000, 891-915 (2003).
    • (2003) J. Chromatogr. A , vol.1000 , pp. 891-915
    • Davankov, V.A.1
  • 10
    • 0035847245 scopus 로고    scopus 로고
    • Protein-based chiral stationary phases for high-performance liquid chromatography enantioseparations
    • Haginaka, J. Protein-based chiral stationary phases for high-performance liquid chromatography enantioseparations, J. Chromatogr. A 906, 253-273 (2001).
    • (2001) J. Chromatogr. A , vol.906 , pp. 253-273
    • Haginaka, J.1
  • 11
    • 0032482102 scopus 로고    scopus 로고
    • Polysaccharide derivatives for chromatographic separation of enantiomers
    • Okamoto, Y. & Yashima, E. Polysaccharide derivatives for chromatographic separation of enantiomers. Angew. Chem. Int. Ed. 37, 1020-1043 (1998).
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1020-1043
    • Okamoto, Y.1    Yashima, E.2
  • 12
    • 84908079528 scopus 로고    scopus 로고
    • Evaluation of perphenylcarbamated cyclodextrin clicked chiral stationary phase for enantioseparations in reversed phase HPLC
    • Pang, L., Zhou, J., Tang, J., Ng, S. C. & Tang, W. Evaluation of perphenylcarbamated cyclodextrin clicked chiral stationary phase for enantioseparations in reversed phase HPLC. J. Chromatogr. A 1363, 119-127 (2014).
    • (2014) J. Chromatogr. A , vol.1363 , pp. 119-127
    • Pang, L.1    Zhou, J.2    Tang, J.3    Ng, S.C.4    Tang, W.5
  • 13
    • 84902419800 scopus 로고    scopus 로고
    • Chromatographic separations and analysis: Cyclodextrin mediated HPLC, GC and CE enantiomeric separations
    • Zhang, X., Zhang, Y. & Armstrong, D. W. Chromatographic separations and analysis: cyclodextrin mediated HPLC, GC and CE enantiomeric separations. Comprehensive Chirality 8, 177-199 (2012).
    • (2012) Comprehensive Chirality , vol.8 , pp. 177-199
    • Zhang, X.1    Zhang, Y.2    Armstrong, D.W.3
  • 15
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C., Finn, M. G. & Sharpless, K. B. Click chemistry: diverse chemical function from a few good reactions. Angew. Chem. Int. Ed. 40, 2004-2021 (2001).
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 16
    • 79954590117 scopus 로고    scopus 로고
    • Application of click chemistry on preparation of separation materials for liquid chromatography
    • Chu, C. & Liu, R. Application of click chemistry on preparation of separation materials for liquid chromatography. Chem. Soc. Rev. 40, 2177-2188 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 2177-2188
    • Chu, C.1    Liu, R.2
  • 17
    • 34250190289 scopus 로고    scopus 로고
    • "Click saccharides": Novel separation materials for hydrophilic interaction liquid chromatography
    • Guo, Z. et al. "Click saccharides": novel separation materials for hydrophilic interaction liquid chromatography. Chem. Commun. 2491-2493 (2007).
    • (2007) Chem. Commun. , pp. 2491-2493
    • Guo, Z.1
  • 18
    • 43049109879 scopus 로고    scopus 로고
    • Preparation of novel ?-cyclodextrin chiral stationary phase based on click chemistry
    • Zhang, Y., Guo, Z., Ye, J., Xu, Q., Liang, X. & Lei, A. Preparation of novel ?-cyclodextrin chiral stationary phase based on click chemistry, J. Chromatogr. A 1191, 188-192 (2008).
    • (2008) J. Chromatogr. A , vol.1191 , pp. 188-192
    • Zhang, Y.1    Guo, Z.2    Ye, J.3    Xu, Q.4    Liang, X.5    Lei, A.6
  • 19
    • 57749114359 scopus 로고    scopus 로고
    • Synthesis, chromatographic evaluation and hydrophilic interaction/reversed-phase mixed-mode behavior of a "click ?-cyclodextrin" stationary phase
    • Guo, Z. et al. Synthesis, chromatographic evaluation and hydrophilic interaction/reversed-phase mixed-mode behavior of a "click ?-cyclodextrin" stationary phase. J. Chromatogr. A 1216, 257-263 (2009).
    • (2009) J. Chromatogr. A , vol.1216 , pp. 257-263
    • Guo, Z.1
  • 20
    • 60649092084 scopus 로고    scopus 로고
    • Enantioseparation of a novel "click" chemistry derived native ?-cyclodextrin chiral stationary phase for high-performance liquid chromatography
    • Wang, Y., Ong, T. T., Li, L.-S., Tan, T. T. Y. & Ng, S. C. Enantioseparation of a novel "click" chemistry derived native ?-cyclodextrin chiral stationary phase for high-performance liquid chromatography. J. Chromatogr. A 1216, 2388-2393 (2009).
    • (2009) J. Chromatogr. A , vol.1216 , pp. 2388-2393
    • Wang, Y.1    Ong, T.T.2    Li, L.-S.3    Tan, T.T.Y.4    Ng, S.C.5
  • 21
    • 77954621576 scopus 로고    scopus 로고
    • "Click" immobilized perphenylcarbamated and permethylated cyclodextrin stationary phases for chiral high-performance liquid chromatography application
    • Wang, Y., Young, D. J., Tan, T. T. Y. & Ng, S. C. "Click" immobilized perphenylcarbamated and permethylated cyclodextrin stationary phases for chiral high-performance liquid chromatography application. J. Chromatogr. A 1217, 5103-5108 (2010).
    • (2010) J. Chromatogr A , vol.1217 , pp. 5103-5108
    • Wang, Y.1    Young, D.J.2    Tan, T.T.Y.3    Ng, S.C.4
  • 22
    • 79959902416 scopus 로고    scopus 로고
    • Preparation of cyclodextrin chiral stationary phases by organic soluble catalytic click chemistry
    • Wang, Y. et al. Preparation of cyclodextrin chiral stationary phases by organic soluble catalytic click chemistry. Nat. Protoc. 6, 935-942 (2011).
    • (2011) Nat. Protoc. , vol.6 , pp. 935-942
    • Wang, Y.1
  • 23
    • 84896358948 scopus 로고    scopus 로고
    • Exploration of ?-cyclodextrin clicked chiral stationary phase in highperformance liquid chromatography
    • Zhang, S., Wang, H., Tang, J., Wang, W. & Tang, W. Exploration of ?-cyclodextrin clicked chiral stationary phase in highperformance liquid chromatography. Anal. Methods 6, 2034-2037 (2014).
    • (2014) Anal. Methods , vol.6 , pp. 2034-2037
    • Zhang, S.1    Wang, H.2    Tang, J.3    Wang, W.4    Tang, W.5
  • 24
    • 4544275995 scopus 로고    scopus 로고
    • Phenylcarbamate derivatives of cellulose and amylase immobilized onto silica gel as chiral stationary phases for high-performance liquid chromatography
    • Kubota, T., Yamamoto, C. & Okamoto, Y. Phenylcarbamate derivatives of cellulose and amylase immobilized onto silica gel as chiral stationary phases for high-performance liquid chromatography. J. Polym. Sci. Part A: Polym. Chem. 42, 4704-4710 (2004).
    • (2004) J. Polym. Sci. Part A: Polym. Chem. , vol.42 , pp. 4704-4710
    • Kubota, T.1    Yamamoto, C.2    Okamoto, Y.3
  • 25
    • 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. 29, 915-923 (2006).
    • (2006) J. Sep. Sci. , vol.29 , pp. 915-923
    • Yamamoto, C.1    Inagaki, S.2    Okamoto, Y.3
  • 26
    • 0029960386 scopus 로고    scopus 로고
    • Dichloro-, dimethyl-, and chloromethylphenylcarbamate derivatives of cyclodextrins as chiral stationary phases for high-performance liquid chromatography
    • Chankvetadze, B., Yashima, E. & Okamoto, Y. Dichloro-, dimethyl-, and chloromethylphenylcarbamate derivatives of cyclodextrins as chiral stationary phases for high-performance liquid chromatography. Chirality 8, 402-407 (1996).
    • (1996) Chirality , vol.8 , pp. 402-407
    • Chankvetadze, B.1    Yashima, E.2    Okamoto, Y.3
  • 27
    • 0038666259 scopus 로고    scopus 로고
    • Partially versus exhaustively carbamoylated cyclodextrins: NMR investigation on enantiodiscriminating capabilities in solution
    • Uccello-Barretta, G., Ferri, L., Balzano, F. & Salvadori, P. Partially versus exhaustively carbamoylated cyclodextrins: NMR investigation on enantiodiscriminating capabilities in solution. Eur. J. Org. Chem. 2003, 1741-1748 (2003).
    • (2003) Eur. J. Org. Chem. , vol.2003 , pp. 1741-1748
    • Uccello-Barretta, G.1    Ferri, L.2    Balzano, F.3    Salvadori, P.4
  • 28
    • 42049117309 scopus 로고    scopus 로고
    • Facile synthesis of mono-6-amino-6-deoxy-?-, ?-, ?-cyclodextrin hydrochlorides for molecular recognition, chiral separation and drug delivery
    • Tang, W. & Ng, S. C. Facile synthesis of mono-6-amino-6-deoxy-?-, ?-, ?-cyclodextrin hydrochlorides for molecular recognition, chiral separation and drug delivery. Nat. Protoc. 3, 691-697 (2008).
    • (2008) Nat. Protoc. , vol.3 , pp. 691-697
    • Tang, W.1    Ng, S.C.2
  • 29
    • 21744441792 scopus 로고    scopus 로고
    • Enantioseparation of dansyl amino acids by a novel permanently positively charged single-isomer cyclodextrin: Mono-6A-N-allylammonium-6A-deoxy-?-cyclodextrin by capillary electrophoresis
    • Tang, W., Muderawan, I. W., Ong, T. T. & Ng, S. C. Enantioseparation of dansyl amino acids by a novel permanently positively charged single-isomer cyclodextrin: mono-6A-N-allylammonium-6A-deoxy-?-cyclodextrin by capillary electrophoresis. Anal. Chim. Acta 546, 119-125 (2005).
    • (2005) Anal. Chim. Acta , vol.546 , pp. 119-125
    • Tang, W.1    Muderawan, I.W.2    Ong, T.T.3    Ng, S.C.4
  • 30
    • 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. A 670, 39-49 (1994).
    • (1994) J. Chromatogr. A , vol.670 , pp. 39-49
    • Chankvetadze, B.1    Yashima, E.2    Okamoto, Y.3
  • 31
    • 80755159495 scopus 로고    scopus 로고
    • Preparation of a novel cyclodextrin derivative of benzimido-?-cyclodextrin and its enantioseparation performance in HPLC
    • Li, X., Zhou, Z., Zhou, W., Dai, L. & Li, Z. Preparation of a novel cyclodextrin derivative of benzimido-?-cyclodextrin and its enantioseparation performance in HPLC. Analyst 136, 5017-5024 (2011).
    • (2011) Analyst , vol.136 , pp. 5017-5024
    • Li, X.1    Zhou, Z.2    Zhou, W.3    Dai, L.4    Li, Z.5
  • 32
    • 84863834855 scopus 로고    scopus 로고
    • Evaluation of novel amylose and cellulose-based chiral stationary phases for the stereoisomer separation of flavanones by means of nano-liquid chromatography
    • Si-Ahmed, K., Aturki, Z., Chankvetadzec, B. & Fanali, S. Evaluation of novel amylose and cellulose-based chiral stationary phases for the stereoisomer separation of flavanones by means of nano-liquid chromatography. Anal. Chim. Acta 738, 85-94 (2012).
    • (2012) Anal. Chim. Acta , vol.738 , pp. 85-94
    • Si-Ahmed, K.1    Aturki, Z.2    Chankvetadzec, B.3    Fanali, S.4
  • 33
    • 19444363540 scopus 로고    scopus 로고
    • High-performance liquid chromatographic separation and chiroptical properties of the enantiomers of naringenin and other flavanones
    • Caccamese, S., Caruso, C., Parrinello, N. & Savarino, A. High-performance liquid chromatographic separation and chiroptical properties of the enantiomers of naringenin and other flavanones. J. Chromatogr. A 1076, 155-162 (2005).
    • (2005) J. Chromatogr. A , vol.1076 , pp. 155-162
    • Caccamese, S.1    Caruso, C.2    Parrinello, N.3    Savarino, A.4
  • 34
    • 33845278694 scopus 로고
    • Computational studies of the interactions of chiral molecules: Complexes of methyl N-(2-naphthyl)alaninate with N-(3,5-dinitrobenzoyl)leucine n-propylamide as a model for chiral stationary-phase interactions
    • Topiol, S., Sabio, M., Moroz, J. & Caldwell, W. B. Computational studies of the interactions of chiral molecules: complexes of methyl N-(2-naphthyl)alaninate with N-(3,5-dinitrobenzoyl)leucine n-propylamide as a model for chiral stationary-phase interactions. J. Am. Chem. Soc. 110, 8376-8385 (1988).
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 8376-8385
    • Topiol, S.1    Sabio, M.2    Moroz, J.3    Caldwell, W.B.4
  • 35
    • 84894637293 scopus 로고    scopus 로고
    • Inclusion complexes of N-sulfamoyloxazolidinones with ?-cyclodextrin: A molecular modeling approach
    • Dinar, K., Sahra, K., Seridi, A. & Kadri, M. Inclusion complexes of N-sulfamoyloxazolidinones with ?-cyclodextrin: A molecular modeling approach. Chem. Phys. Lett. 595-596, 113-120 (2014).
    • (2014) Chem. Phys. Lett. , vol.595-596 , pp. 113-120
    • Dinar, K.1    Sahra, K.2    Seridi, A.3    Kadri, M.4


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