Use of hydroxypropyl- and hydroxyethyl-derivatized β-cyclodextrins for the thin-layer chromatographic separation of enantiomers and diastereomers
- 1 October 1988
- journal article
- research article
- Published by Elsevier in Journal of Chromatography A
- Vol. 452, 323-330
- https://doi.org/10.1016/s0021-9673(01)81457-6
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Direct liquid chromatographic separation of racemates with an .alpha.-cyclodextrin bonded phaseAnalytical Chemistry, 1987
- Optical isomer separation by liquid chromatographyAnalytical Chemistry, 1987
- 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
- Synthesis, rapid resolution, and determination of absolute configuration of racemic 2,2'-binaphthyldiyl crown ethers and analogs via .beta.-cyclodextrin complexationThe Journal of Organic Chemistry, 1985
- Separation of Metallocene Enantiomers by Liquid Chromatography: Chiral Recognition Via Cyclodextrin Bonded PhasesAnalytical Chemistry, 1985
- Liquid chromatographic separation of enantiomers using a chiral .beta.-cyclodextrin-bonded stationary phase and conventional aqueous-organic mobile phasesAnalytical Chemistry, 1985
- Liquid chromatographic separation of diastereomers and structural isomers on cyclodextrin-bonded phasesAnalytical Chemistry, 1985
- Chiral Stationary Phases for High Performance Liquid Chromatographic Separation of Enantiomers: A Mini-ReviewJournal of Liquid Chromatography, 1984