CAPILLARY ELECTROPHORETIC CHIRAL RESOLUTION OF VICINAL DIOLS BY COMPLEXATION WITH BORATE AND CYCLODEXTRIN - COMPARATIVE-STUDIES ON DIFFERENT CYCLODEXTRIN DERIVATIVES
Mg. Schmid et al., CAPILLARY ELECTROPHORETIC CHIRAL RESOLUTION OF VICINAL DIOLS BY COMPLEXATION WITH BORATE AND CYCLODEXTRIN - COMPARATIVE-STUDIES ON DIFFERENT CYCLODEXTRIN DERIVATIVES, Chirality, 9(2), 1997, pp. 153-156
Capillary electrophoretic enantioseparation of compounds containing vi
cinal diol groups have been investigated using different beta-cyclodex
trin (CD) derivatives and berate as a background electrolyte. Both nat
ive beta-CD and several beta-CD derivatives are examined. Chiral recog
nition is attributed to both enantioselective inclusion of the analyte
into the chiral cavity of the CD and complexation with berate. The in
fluence of concentration of the chiral selector, pH, and organic modif
iers on the resolution was studied. Four diols were baseline separated
. (C) 1997 Wiley-Liss, Inc.