Determination Enantiomer Excess (e.e. %) of Chiral Sharpless Epoxides with β-Cyclodextrin Derivatives as Chiral Stationary Phases of Capillary Gas Chromatography
Xueyan Shi, Pei Liang, Xiwu Gao
Abstract
Xueyan Shi, Pei Liang, Xiwu Gao
Abstract
Using four β-cyclodextrin derivatives, 2,6-di-O-benzyl-3-O-heptanonyl-β-CD, 2,6-di-O-benzyl-3-O-octanonyl-β-CD, 2,3-di-O-benzyl-6-O-heptanonyl-β-CD, and 2,3-di-O-benzyl-6-O-octanonyl-3-CD, as chiral stationary phases of capillary gas chromatography (CGC), the enantiomers of Sharpless epoxides were well separated. The enantiomer excess values (e.e.%) of some chiral Sharpless epoxides were also determined successfully using these CDs.
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Using four β-cyclodextrin derivatives, 2,6-di-O-benzyl-3-O-heptanonyl-β-CD, 2,6-di-O-benzyl-3-O-octanonyl-β-CD, 2,3-di-O-benzyl-6-O-heptanonyl-β-CD, and 2,3-di-O-benzyl-6-O-octanonyl-3-CD, as chiral stationary phases of capillary gas chromatography (CGC), the enantiomers of Sharpless epoxides were well separated. The enantiomer excess values (e.e.%) of some chiral Sharpless epoxides were also determined successfully using these CDs.
Key concepts: Chemistry, Enantiomer, Cyclodextrin, Capillary gas chromatography, Gas chromatography, Chiral column chromatography, Chromatography, Organic chemistry