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Volumn 15, Issue 5, 2003, Pages 429-432

Conversion of a racemic mixture of 8-chloro-2-(2,6-difluorophenylmethyl)- 2,3-dihydro-3-methyl-1,2,5-benzothiadiazepin-4(5H)-one 1,1-dioxide into a single enantiomer via a chromatographic resolution/racemization method

Author keywords

Enantiomer separation; Free energy barrier; Polyacrylamide derivative; Racemization; Rate constant

Indexed keywords

8 CHLORO 2 (2,6 DIFLUOROPHENYLMETHYL) 2,3 DIHYDRO 3 METHYL 1,2,5 BENZOTHIADIAZEPIN 4(5H) ONE 1,1 DIOXIDE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; POLYACRYLAMIDE; RNA DIRECTED DNA POLYMERASE; UNCLASSIFIED DRUG;

EID: 0037277248     PISSN: 08990042     EISSN: None     Source Type: Journal    
DOI: 10.1002/chir.10226     Document Type: Article
Times cited : (7)

References (11)
  • 1
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    • Enantioselective chromatography as a powerful alternative for the preparation of drug enantiomers
    • Francotte ER. Enantioselective chromatography as a powerful alternative for the preparation of drug enantiomers. J Chromatogr A 2001; 906:379-397.
    • (2001) J Chromatogr A , vol.906 , pp. 379-397
    • Francotte, E.R.1
  • 2
    • 0037080854 scopus 로고    scopus 로고
    • Pharmaceutical and biomedical applications of enantioseparations using liquid chromatographic techniques
    • Haginaka J. Pharmaceutical and biomedical applications of enantioseparations using liquid chromatographic techniques. J Pharm Biomed Anal 2002;27:357-372.
    • (2002) J Pharm Biomed Anal , vol.27 , pp. 357-372
    • Haginaka, J.1
  • 4
    • 0030737815 scopus 로고    scopus 로고
    • Controlled racemization of optically active organic compounds: Prospect for asymmetric transformation
    • Ebbers EJ, Ariaans GJA, Houbiers JPM, Bruggink A, Zwanenburg B. Controlled racemization of optically active organic compounds: prospect for asymmetric transformation. Tetrahedron 1997;53:9417-9476.
    • (1997) Tetrahedron , vol.53 , pp. 9417-9476
    • Ebbers, E.J.1    Ariaans, G.J.A.2    Houbiers, J.P.M.3    Bruggink, A.4    Zwanenburg, B.5
  • 9
    • 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 1998;37:1020-1043.
    • (1998) Angew Chem Int Ed , vol.37 , pp. 1020-1043
    • Okamoto, Y.1    Yashima, E.2
  • 10
    • 0032940574 scopus 로고    scopus 로고
    • Enantioseparations in normal- and reversed-phase nano-high-performance liquid chromatography and capillary electrocromatography using polyacrylamide and polysaccharide derivatives as chiral stationary phases
    • Krause K, Girod M, Chankvetadze B, Blaschke G. Enantioseparations in normal- and reversed-phase nano-high-performance liquid chromatography and capillary electrocromatography using polyacrylamide and polysaccharide derivatives as chiral stationary phases. J Chromatogr A 1999;837:51-63.
    • (1999) J Chromatogr A , vol.837 , pp. 51-63
    • Krause, K.1    Girod, M.2    Chankvetadze, B.3    Blaschke, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.