The enantiomers of 7-des-methyl-ormeloxifene were separated by countercurrent chromatography (CCC) using sulfated β€-cyclodextrin as chiral selector, representing the first reported successful application of a cyclodextrin derivative in CCCbased resolutions. The choice of chiral selector relies on ex
Separation of enantiomers using vancomycin in a countercurrent process by suppression of electroosmosis
β Scribed by Timothy J. Ward; Charles Dann III; Andy P. Brown
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 442 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0899-0042
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β¦ Synopsis
Excellent separations were achieved using a coated column to suppress electroosmotic flow and employing a countercurrent process between chiral selector and racemic solute. Using the macrocyclic antibiotic vancomycin as a chiral selector in capillary electrophoresis the resolution of nonsteroidal antiinflammatories and dansyl amino acids was achieved. Improvement in sensitivity due to the elimination of background absorbance and increased efficiency due to the removal of wall adsorption effects are both achieved using this technique.
π SIMILAR VOLUMES
Chiral separation of basic compounds was achieved by using 75 or 100 microm ID fused-silica capillaries packed with a vanoomycin-modified diol silica stationary phase. The capillary was firstly packed for about 12 cm with a slurry mixture composed of diolsilica (3:1) then with the vancomycin modifie