Several cyclic imidic compounds (barbiturates, piperidine-2,6-diones, and mephenytoin) are enantiomerically resolved via high-performance liquid chromatography (HPLC) on a macrocyclic antibiotic covalently bonded to a silica gel support. The Chirobiotic V chiral stationary phase (CSP) column contain
Enantioseparation of kavain on Chiralpak IA under normal-phase, polar organic and reversed-phase conditions
✍ Scribed by Roberto Cirilli; Rosella Ferretti; Bruno Gallinella; Anna Rita Bilia; Franco Francesco Vincieri; Francesco La Torre
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 780 KB
- Volume
- 31
- Category
- Article
- ISSN
- 1615-9306
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✦ Synopsis
Abstract
First baseline HPLC enantioseparation of kavain is described. Complete enantiodiscrimination was achieved on the immobilised‐type Chiralpak IA chiral stationary phase (CSP) using pure methanol and simple methanol‐water and ethanol‐water mixtures as eluents. A water‐dependent enantioselectivity was clearly demonstrated. Performance of the Chiralpak IA CSP in polar organic and RP conditions was compared with that of five coated polysaccharide‐derived CSPs used in normal‐phase mode.
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