Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0040-4039(01)02147-5
Title: Facile preparative HPLC enantioseparation of racemic drugs using chiral stationary phases based on mono-6A-azido-6A-deoxy-perphenylcarbamoylated β-cyclodextrin immobilized on silica gel
Authors: Ng, S.-C. 
Chen, L.
Zhang, L.-F.
Ching, C.-B. 
Keywords: β-cyclodextrin
Enantioseparation
HPLC
Preparative
Issue Date: 21-Jan-2002
Citation: Ng, S.-C., Chen, L., Zhang, L.-F., Ching, C.-B. (2002-01-21). Facile preparative HPLC enantioseparation of racemic drugs using chiral stationary phases based on mono-6A-azido-6A-deoxy-perphenylcarbamoylated β-cyclodextrin immobilized on silica gel. Tetrahedron Letters 43 (4) : 677-681. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(01)02147-5
Abstract: Immobilized chiral stationary phases (CSP)s from mono-6A-azido-6A-deoxy-perphenylcarbamoylated β-cyclodextrin were prepared using an extended application of the Staudinger reaction. Their application in preparative enantioseparations of racemic mixtures was demonstrated using atropine, bendroflumethiazide and four β-adrenergic blocking agents under reversed phase conditions. © 2002 Published by Elsevier Science Ltd.
Source Title: Tetrahedron Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/91986
ISSN: 00404039
DOI: 10.1016/S0040-4039(01)02147-5
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