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D. Armstrong, K. Rundlett (1995)
CE Resolution of Neutral and Anionic Racemates with Glycopeptide Antibiotics and MicellesJournal of Liquid Chromatography & Related Technologies, 18
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Use of a macrocyclic antibiotic, rifamycin B, and indirect detection for the resolution of racemic amino alcohols by CE.Analytical chemistry, 66 10
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Highly enantioselective capillary electrophoretic separations with dilute solutions of the macrocyclic antibiotic ristocetin A.Journal of chromatography. A, 689 2
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Comparison and modelling study of vancomycin, ristocetin A and teicoplanin for CE enantioseparations, 68
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Enantiomeric resolution using the macrocyclic antibiotics rifamycin B and rifamycin SV as chiral selectors for capillary electrophoresis.Journal of chromatography. A, 715 2
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The macrocyclic glycopeptide, ristocetin A, was covalently bonded to a silica gel support and evaluated as a liquid chromatographic (LC) chiral stationary phase (CSP). Over 230 racemates were resolved in either the reversed‐phase mode, the normal‐phase mode, or the polar‐organic mode. The retention behavior and selectivity of this CSP were examined in each mode. Optimization of separations on this column is discussed. The ristocetin A CSP appeared to be complimentary to other glycopeptide CSPs (i.e., vancomycin and teicoplanin). Column stability was excellent. The CSP was not irreversibly altered when going from one mobile phase mode to another. Chirality 10:434–483, 1998. © 1998 Wiley‐Liss, Inc.
Chirality – Wiley
Published: Jan 1, 1998
Keywords: ; ; ; ;
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