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  • Title: Separation of chiral 4-substituted imidazole derivatives by cyclodextrin-modified capillary electrophoresis.
    Author: Sasse A, Schunack W, Stark H.
    Journal: Biomed Chromatogr; 2001 Feb; 15(1):25-30. PubMed ID: 11180297.
    Abstract:
    Enantiomeric separations by cyclodextrin-modified capillary electrophoresis of chiral carbamates containing a 4-substituted imidazole heterocycle, pharmacologically acting as histamine H3-receptor antagonists, were carried out. Various cyclodextrins (alpha-, beta- and substituted beta-cyclodextrins) were investigated. Baseline resolution was achieved with six out of 11 compounds. Heptakis-2,3,6-trimethyl-beta-cyclodextrin modified buffers seemed to be most efficient in separating most of the investigated compounds. The optical purity of one pair of enantiomers was determined.
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