Two new chiral selectors, obtained by derivatising two of the three hydroxyl groups of the cholic acid with 2-naphthylisocyanate and 3,5-dinitrophenylisocyanate, have been prepared and linked to silica gel to obtain chiral stationary phases (CSPs) for the HPLC separation of enantiomers. The enantodiscriminating capability of the two CSPs has been compared to that of the analogous CSP obtained from an exhaustively derivatised cholic acid based selector, in order to establish the effect of the presence of a free hydroxyl group on the enantiodiscrimination properties of this kind of selectors. The chromatographic results demonstrate that the enantioselectivity of these selectors strongly depends on the position of the hydroxyl group on the cholestanic backbone.
Effect of the presence of a free hydroxyl group on the enantiodiscrimination properties of cholic acid based CSPs bearing 2-naphthylcarbamate and 3,5-dinitrophenylcarbamate moieties in the HPLC resolution of racemic compounds
IULIANO, ANNA;
2005-01-01
Abstract
Two new chiral selectors, obtained by derivatising two of the three hydroxyl groups of the cholic acid with 2-naphthylisocyanate and 3,5-dinitrophenylisocyanate, have been prepared and linked to silica gel to obtain chiral stationary phases (CSPs) for the HPLC separation of enantiomers. The enantodiscriminating capability of the two CSPs has been compared to that of the analogous CSP obtained from an exhaustively derivatised cholic acid based selector, in order to establish the effect of the presence of a free hydroxyl group on the enantiodiscrimination properties of this kind of selectors. The chromatographic results demonstrate that the enantioselectivity of these selectors strongly depends on the position of the hydroxyl group on the cholestanic backbone.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
