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|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.
|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|
|Appears in Collections:||Staff Publications|
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