(R)- and (S)-Naphthylethylcarbamate-substituted β-cyclo-dextrin bonded stationary phases for the reversed-phase liquid chromatographic separation of enantiomers
- 31 December 1991
- journal article
- Published by Elsevier in Journal of Chromatography A
- Vol. 539 (1) , 83-90
- https://doi.org/10.1016/s0021-9673(01)95362-2
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Direct liquid chromatographic separation of enantiomers on immobilized protein stationary phases : III. Optical resolution of a series of N-aroyl d,l-amino acids by high-performance liquid chromatography on bovine serum albumin covalently bound to silicaPublished by Elsevier ,2001
- Derivatized cyclodextrins for normal-phase liquid chromatographic separation of enantiomersAnalytical Chemistry, 1990
- Chromatographic resolution: XXI. Direct optical resolution of abscisic acid by high-performance liquid chromatography on cellulose tris(3,5-dimethylphenylcarbamate)Journal of Chromatography A, 1988
- Chromatographic chiral resolutionJournal of Chromatography A, 1987
- Normal-phase high-performance liquid chromatographic separations of positional isomers of substituted benzoic acids with amine and β-cyclodextrin bonded-phase columnsJournal of Chromatography A, 1986
- Reversed-phase chromatographic resolution of N-(3,5-dinitrobezoyl)- α-amino acids on chiral stationary phasesJournal of Chromatography A, 1985
- Cyclodextrin Bonded Phases For the Liquid Chromatographic Separation of Optical, Geometrical, and Structural IsomersJournal of Chromatographic Science, 1984
- Direct liquid chromatographic resolution of racemic drugs using α1-acid glycoprotein as the chiral stationary phaseJournal of Chromatography A, 1983