Gas chromatographic separation of chrysanthemic acid ester enantiomers on a novel chiral stationary phase
- 31 December 1983
- journal article
- research article
- Published by Elsevier in Journal of Chromatography A
- Vol. 254, 282-284
- https://doi.org/10.1016/s0021-9673(01)88344-8
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Some N-acyl derivatives of 1-(α-naphthyl)ethylamine as stationary phases for the separation of optical isomers in gas chromatographyJournal of Chromatography A, 1982
- N-(1R,3R)-trans-chrysanthemoyl (R)-1-(α-naphthyl)ethylamine as a stationary phase for the separation of optical isomers by gas chromatographyJournal of Chromatography A, 1981
- Gas chromatographic separation of α-hydroxycarbolic acid ester enantiometers using amino acid derivatives as chiral stationary phaseJournal of Chromatography A, 1981
- Structural requirements for enantioselectivity in gas chromatography of chiral α-hydroxy acidsJournal of Chromatography A, 1980
- Separation of the Enantiomers of 2‐Hydroxycarboxylic Acids on Optically Active Stationary PhasesAngewandte Chemie International Edition in English, 1980