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Volumn 1467, Issue , 2016, Pages 214-220

Preparation and evaluation of immobilized 4-methylbenzoylcellulose stationary phases for enantioselective separations

Author keywords

Chiral stationary phases; Enantioselective chromatography; Immobilized polysaccharides

Indexed keywords

ENANTIOSELECTIVITY; LIQUID CHROMATOGRAPHY; MOLECULES; SEPARATION; SILICA GEL; STEREOCHEMISTRY;

EID: 84991078980     PISSN: 00219673     EISSN: 18733778     Source Type: Journal    
DOI: 10.1016/j.chroma.2016.08.006     Document Type: Article
Times cited : (14)

References (22)
  • 2
    • 84890704606 scopus 로고    scopus 로고
    • Chiral stationary phases for preparative enantioselective chromatography
    • G.B. Cox Blackwell Publishing Oxford
    • [2] Francotte, E., Chiral stationary phases for preparative enantioselective chromatography. Cox, G.B., (eds.) Preparative Enantioselective Chromatography, 2005, Blackwell Publishing, Oxford, 48–77.
    • (2005) Preparative Enantioselective Chromatography , pp. 48-77
    • Francotte, E.1
  • 3
    • 26844485913 scopus 로고    scopus 로고
    • Polysaccharide-based chiral LC columns
    • [3] Yashima, E., Yamamoto, C., Okamoto, Y., Polysaccharide-based chiral LC columns. Synlett, 1998, 344–360.
    • (1998) Synlett , pp. 344-360
    • Yashima, E.1    Yamamoto, C.2    Okamoto, Y.3
  • 4
    • 34250883083 scopus 로고    scopus 로고
    • Preparative Enantioselective Chromatography
    • Blackwell Publishing Oxford
    • [4] Cox, G.B., Preparative Enantioselective Chromatography. 2005, Blackwell Publishing, Oxford.
    • (2005)
    • Cox, G.B.1
  • 5
    • 0035847205 scopus 로고    scopus 로고
    • Enantioselective chromatography as a powerful alternative for the ‘Preparation’ of drug enantiomers
    • [5] Francotte, E., Enantioselective chromatography as a powerful alternative for the ‘Preparation’ of drug enantiomers. J. Chromatogr. A 906 (2001), 379–397.
    • (2001) J. Chromatogr. A , vol.906 , pp. 379-397
    • Francotte, E.1
  • 6
    • 0028331505 scopus 로고
    • Resolution by high-performance liquid chromatography using polysaccharide carbamates and benzoates as chiral stationary phases
    • [6] Okamoto, Y., Kaida, Y., Resolution by high-performance liquid chromatography using polysaccharide carbamates and benzoates as chiral stationary phases. J. Chromatogr. A 666 (1994), 403–419.
    • (1994) J. Chromatogr. A , vol.666 , pp. 403-419
    • Okamoto, Y.1    Kaida, Y.2
  • 7
    • 0032482102 scopus 로고    scopus 로고
    • Polysaccharide derivatives for chromatographic separation of enantiomers
    • [7] Okamoto, Y., Yashima, E., Polysaccharide derivatives for chromatographic separation of enantiomers. Angew. Chem. Int. Ed. 37 (1998), 1020–1043.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1020-1043
    • Okamoto, Y.1    Yashima, E.2
  • 8
    • 0035847277 scopus 로고    scopus 로고
    • Polysaccharide-based chiral stationary phases for high-performance liquid chromatographic enantioseparation
    • [8] Yashima, E., Polysaccharide-based chiral stationary phases for high-performance liquid chromatographic enantioseparation. J. Chromatogr. A 906 (2001), 105–125.
    • (2001) J. Chromatogr. A , vol.906 , pp. 105-125
    • Yashima, E.1
  • 9
    • 1542350269 scopus 로고    scopus 로고
    • Optically active polymers for chiral separation
    • [9] Yamamoto, C., Okamoto, Y., Optically active polymers for chiral separation. Bull. Chem. Soc. Jpn. 77 (2004), 227–257.
    • (2004) Bull. Chem. Soc. Jpn. , vol.77 , pp. 227-257
    • Yamamoto, C.1    Okamoto, Y.2
  • 10
    • 84958093894 scopus 로고    scopus 로고
    • Efficient separation of enantiomers using stereoregular chiral polymers
    • [10] Shen, J., Okamoto, Y., Efficient separation of enantiomers using stereoregular chiral polymers. Chem. Rev. 116 (2016), 1094–1138.
    • (2016) Chem. Rev. , vol.116 , pp. 1094-1138
    • Shen, J.1    Okamoto, Y.2
  • 11
    • 33645748956 scopus 로고    scopus 로고
    • Immobilized polysaccharide-based chiral stationary phases for HPLC
    • [11] Ikai, T., Yamamoto, C., Kamigaito, M., Okamoto, Y., Immobilized polysaccharide-based chiral stationary phases for HPLC. Polym. J. 38 (2006), 91–108.
    • (2006) Polym. J. , vol.38 , pp. 91-108
    • Ikai, T.1    Yamamoto, C.2    Kamigaito, M.3    Okamoto, Y.4
  • 12
    • 0023175366 scopus 로고
    • Chiral stationary phases for HPLC: cellulose tris(3,5-dimethylphenylcarbamate) and tris(3,5-dichlorophenylcarbamate) chemically bonded to silica gel
    • [12] 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. 10 (1987), 1613–1628.
    • (1987) J. Liq. Chromatogr. , vol.10 , pp. 1613-1628
    • Okamoto, Y.1    Aburatani, R.2    Miura, S.3    Hatada, K.4
  • 13
    • 79960833676 scopus 로고    scopus 로고
    • Improved preparation of chiral stationary phases via immobilization of polysaccharide derivative-based selectors using diisocyanates
    • [13] Tang, Shouwan, Liu, G., Li, X., Jin, Z., Wang, F., Pan, F., Okamoto, Y., Improved preparation of chiral stationary phases via immobilization of polysaccharide derivative-based selectors using diisocyanates. J. Sep. Sci. 34 (2011), 1763–1771.
    • (2011) J. Sep. Sci. , vol.34 , pp. 1763-1771
    • Tang, S.1    Liu, G.2    Li, X.3    Jin, Z.4    Wang, F.5    Pan, F.6    Okamoto, Y.7
  • 14
    • 79952023683 scopus 로고    scopus 로고
    • Preparation and chiral recognition in HPLC of cellulose 3,5-dichlorophenylcarbamates immobilized onto silica gel
    • [14] Qu, H.-T., Li, J.-G., Wu, G.-S., Shen, J., Shen, X.-D., Okamoto, Y., Preparation and chiral recognition in HPLC of cellulose 3,5-dichlorophenylcarbamates immobilized onto silica gel. J. Sep. Sci. 34 (2011), 536–541.
    • (2011) J. Sep. Sci. , vol.34 , pp. 536-541
    • Qu, H.-T.1    Li, J.-G.2    Wu, G.-S.3    Shen, J.4    Shen, X.-D.5    Okamoto, Y.6
  • 15
    • 58149156497 scopus 로고    scopus 로고
    • Immobilization of cellulose phenylcarbamate onto silica gel via intermolecular polycondensation of triethoxysilyl groups introduced with (3-glycidoxypropyl)triethoxysilane
    • [15] Tang, S., Okamoto, Y., Immobilization of cellulose phenylcarbamate onto silica gel via intermolecular polycondensation of triethoxysilyl groups introduced with (3-glycidoxypropyl)triethoxysilane. J. Sep. Sci. 31 (2008), 3133–3138.
    • (2008) J. Sep. Sci. , vol.31 , pp. 3133-3138
    • Tang, S.1    Okamoto, Y.2
  • 16
    • 84991063978 scopus 로고    scopus 로고
    • Photochemically cross-linked polysaccharide derivatives as supports for the chromatographic separation of enantiomers, Patent (1996) WO 9627615 A1.
    • [16] E. Francotte, Photochemically cross-linked polysaccharide derivatives as supports for the chromatographic separation of enantiomers, Patent (1996) WO 9627615 A1.
    • Francotte, E.1
  • 17
    • 84991055756 scopus 로고    scopus 로고
    • Maleimide derivatives, Patent Ger. Offen. (1976) DE 2626795 A1 1976 1230
    • [17] M. Baumann, V. Kvita, M. Roth, J.S. Waterhouse, Maleimide derivatives, Patent Ger. Offen. (1976) DE 2626795 A1 1976 1230.
    • Baumann, M.1    Kvita, V.2    Roth, M.3    Waterhouse, J.S.4
  • 18
    • 0029565116 scopus 로고
    • Supramolecular effects in the chiral discrimination of meta-methylbenzoyl cellulose in high-performance liquid chromatography
    • [18] Francotte, E., Zhang, T., Supramolecular effects in the chiral discrimination of meta-methylbenzoyl cellulose in high-performance liquid chromatography. J. Chromatog. A 718 (1995), 257–266.
    • (1995) J. Chromatog. A , vol.718 , pp. 257-266
    • Francotte, E.1    Zhang, T.2
  • 19
    • 0012003562 scopus 로고
    • Useful chiral packing materials for high-performance liquid chromatographic resolution of enantiomers: phenylcarbamates of polysaccharides coated on silica gel
    • [19] 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. 106 (1984), 5357–5359.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 5357-5359
    • Okamoto, Y.1    Kawashima, M.2    Hatada, K.3
  • 20
    • 84981886823 scopus 로고
    • A new class of photopolymers with pendent dimethylmaleimide groups III. Comparative study of different photopolymers with pendent olefinic structures including dimethylmaleimide groups
    • [20] Finter, J., Haniotis, Z., Lohse, F., Meier, K., Zweifel, H., A new class of photopolymers with pendent dimethylmaleimide groups III. Comparative study of different photopolymers with pendent olefinic structures including dimethylmaleimide groups. Angew. Makromol. Chem. 133 (1985), 147–170.
    • (1985) Angew. Makromol. Chem. , vol.133 , pp. 147-170
    • Finter, J.1    Haniotis, Z.2    Lohse, F.3    Meier, K.4    Zweifel, H.5
  • 21
    • 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
    • [21] 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. 68 (1996), 2798–2804.
    • (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
  • 22
    • 0037080865 scopus 로고    scopus 로고
    • Immobilized halogeno-phenylcarbamate derivatives of cellulose as novel chiral stationary phases for enantioselective drug analysis
    • [22] Francotte, E., Huynh, D., Immobilized halogeno-phenylcarbamate derivatives of cellulose as novel chiral stationary phases for enantioselective drug analysis. J. Pharm. Biomed. Anal. 27 (2002), 421–429.
    • (2002) J. Pharm. Biomed. Anal. , vol.27 , pp. 421-429
    • Francotte, E.1    Huynh, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.