Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.chroma.2003.11.018
Title: Preparation and chiral recognition of a novel chiral stationary phase for high-performance liquid chromatography, based on mono(6A-N- allylamino-6A-deoxy)-perfunctionalized β-cyclodextrin and covalently bonded silica gel
Authors: Lai, X.-H.
Ng, S.-C. 
Keywords: Alcohols
Beta-blockers
Chiral stationary phases, LC
Cyclodextrins
Drugs
Pyrimidines
Issue Date: 26-Mar-2004
Citation: Lai, X.-H., Ng, S.-C. (2004-03-26). Preparation and chiral recognition of a novel chiral stationary phase for high-performance liquid chromatography, based on mono(6A-N- allylamino-6A-deoxy)-perfunctionalized β-cyclodextrin and covalently bonded silica gel. Journal of Chromatography A 1031 (1-2) : 135-142. ScholarBank@NUS Repository. https://doi.org/10.1016/j.chroma.2003.11.018
Abstract: A novel chiral stationary phase (CSP) was prepared by immobilizing mono(6A-N-allylamino-6A-deoxy)-perphenylcarbamoylated β-cyclodextrin onto the surface of silica gel via hydrosilylation. The chromatographic properties of this column were tested with a wide range of structurally diverse racemic compounds and drugs under reverse phases. Separation mechanisms involved are also discussed. © 2003 Published by Elsevier B.V.
Source Title: Journal of Chromatography A
URI: http://scholarbank.nus.edu.sg/handle/10635/94597
ISSN: 00219673
DOI: 10.1016/j.chroma.2003.11.018
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