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基于单(6A-N-烯丙基氨基-6A-脱氧)-全功能化β-环糊精和共价键合硅胶的新型高效液相色谱手性固定相的制备及手性识别

Preparation and chiral recognition of a novel chiral stationary phase for high-performance liquid chromatography, based on mono(6A-N-allylamino-6A-deoxy)-perfunctionalized beta-cyclodextrin and covalently bonded silica gel.

作者信息

Lai Xiang-Hua, Ng Siu-Choon

机构信息

Department of Chemistry, National University of Singapore, Singapore 119260, Singapore.

出版信息

J Chromatogr A. 2004 Mar 26;1031(1-2):135-42. doi: 10.1016/j.chroma.2003.11.018.

DOI:10.1016/j.chroma.2003.11.018
PMID:15058577
Abstract

A novel chiral stationary phase (CSP) was prepared by immobilizing mono(6A-N-allylamino-6A-deoxy)-perphenylcarbamoylated beta-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.

摘要

通过硅氢加成反应将单(6A-N-烯丙基氨基-6A-脱氧)-全苯基氨基甲酰化β-环糊精固定在硅胶表面,制备了一种新型手性固定相(CSP)。在反相条件下,用多种结构不同的外消旋化合物和药物对该柱的色谱性能进行了测试。还讨论了所涉及的分离机制。

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