Issue 4, 2001

Enantioselective separation of epoxides by capillary electrophoresis employing sulfated ß-cyclodextrin as chiral selector

Abstract

A capillary electrophoresis method was developed for the enantioseparation of epoxide compounds. Sulfated β-cyclodextrin was employed as a chiral selector. Phosphate–triethanolamine buffer showed a chiral separation effect when employing charged sulfated β-cyclodextrin. The effect of pH, triethanolamine concentration and sulfated β-cyclodextrin concentration on the resolution was studied. Methanol was tested as an organic modifier. Several other epoxides were successfully separated by the proposed method.

Article information

Article type
Paper
Submitted
04 Jan 2001
Accepted
26 Jan 2001
First published
09 Mar 2001

Analyst, 2001,126, 438-440

Enantioselective separation of epoxides by capillary electrophoresis employing sulfated ß-cyclodextrin as chiral selector

W. Jianjun, Z. Guojun, Y. Liu and S. Wanru, Analyst, 2001, 126, 438 DOI: 10.1039/B100205H

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