High-performance liquid Chromatographic separation of the enantiomers of N-aryloxazolinones, N-aryl thiazolinones and their sulfur derivatives on a synthetic chiral stationary phase
- 1 March 1996
- journal article
- Published by Elsevier in Journal of Chromatography A
- Vol. 726 (1-2) , 91-97
- https://doi.org/10.1016/0021-9673(95)00949-3
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Use of simultaneous face to face and face to edge π-π interactions to facilitate chiral recognitionTetrahedron: Asymmetry, 1994
- An Improved Chiral Stationary Phase for the Chromatographic Separation of Underivatized Naproxen EnantiomersJournal of Liquid Chromatography, 1992
- Design, synthesis, and evaluation of an improved enantioselective naproxen selectorThe Journal of Organic Chemistry, 1992
- Example of the concentration dependence of elution order in the resolution of enantiomers on microcrystalline triacetylcellulose chiral stationary phaseJournal of Chromatography A, 1989
- Comparison of racemization processes in 1-arylpyrimidine-2-thione and 3-arylthiazoline-2-thione atropisomers and their oxygen analogsThe Journal of Organic Chemistry, 1988
- Conformational analysis of trigonal and planar rotors attached to Δ4-azoline-2-thiones. The effect of ring geometryJournal of the Chemical Society, Perkin Transactions 2, 1985
- Reactions of Propargyl Alcohols and Propargylamines with IsocyanatesThe Journal of Organic Chemistry, 1963
- Reactions of Acetylenes. I. t-Ethynyl Alcohol with IsocyanatesThe Journal of Organic Chemistry, 1962
- Cyclization of N-Phenylcarbamates of EthynylcarbinolsThe Journal of Organic Chemistry, 1962