Resolution of chiral barbiturates into enantiomers by reversed-phase high-performance liquid chromatography using methylated β-cyclodextrins
- 1 January 1988
- journal article
- research article
- Published by Elsevier in Journal of Chromatography A
- Vol. 436 (3) , 381-390
- https://doi.org/10.1016/s0021-9673(00)94597-7
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Separation of Drug Stereoisomers by the Formation of β-Cyclodextrin Inclusion ComplexesScience, 1986
- Resolution of Mephenytoin and Some Chiral Barbiturates into Enantiomers by Reversed Phase High Performance Liquid Chromatography via β-Cyclodextrin Inclusion ComplexesJournal of Liquid Chromatography, 1986
- Improved Cyclodextrin Chiral Phases: A Comparison and ReviewJournal of Liquid Chromatography, 1986
- Resolution of ortho, meta, and para isomers of some disubstituted benzene derivatives via .alpha.- and .beta.-cyclodextrin inclusion complexes, using reversed-phase high-performance liquid chromatographyAnalytical Chemistry, 1985
- Liquid chromatographic separation of enantiomers using a chiral .beta.-cyclodextrin-bonded stationary phase and conventional aqueous-organic mobile phasesAnalytical Chemistry, 1985
- Chiral Stationary Phases for High Performance Liquid Chromatographic Separation of Enantiomers: A Mini-ReviewJournal of Liquid Chromatography, 1984
- Interaction of barbiturates with benzodiazepine receptors in the central nervous systemBrain Research, 1982
- Mechanism of Action of BarbituratesAnnual Review of Pharmacology and Toxicology, 1981
- Synthesis and 13C‐NMR Spectroscopy of Methylated beta‐CyclodextrinsStarch ‐ Stärke, 1980
- Methylated cycloamyloses (cyclodextrins) and their inclusion propertiesCarbohydrate Research, 1979