Liquid chromatographic separation of the enantiomers of dinitrophenyl amino acids using a β-cyclodextrin-bonded stationary phase
- 1 January 1991
- journal article
- Published by Elsevier in Journal of Chromatography A
- Vol. 543, 105-112
- https://doi.org/10.1016/s0021-9673(01)95758-9
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Direct liquid chromatographic separation of racemates with an .alpha.-cyclodextrin bonded phaseAnalytical Chemistry, 1987
- Geometry of cyclohexaamylose inclusion complexes with some substituted benzenes in aqueous solution based on carbon-13 NMR chemical shiftsJournal of the American Chemical Society, 1985
- Liquid chromatographic separation of enantiomers using a chiral .beta.-cyclodextrin-bonded stationary phase and conventional aqueous-organic mobile phasesAnalytical Chemistry, 1985
- Photophysical investigations of chiral amine guest-cyclodextrin host interactions and diastereomeric recognitionThe Journal of Physical Chemistry, 1984
- Accumulation of D-Aspartic Acid with Age in the Human BrainScience, 1983
- Chiral host–guest complexes: interaction of α-cyclodextrin with optically active benzene derivativesJournal of the Chemical Society, Perkin Transactions 2, 1978
- Retention of configuration in the solid phase synthesis of peptidesJournal of the American Chemical Society, 1970
- THE EXTRACTION OF TETRAALKYLAMMONIUM HYDROXIDES AND THE SOLVATION OF THE HYDROXIDE ION1aThe Journal of Physical Chemistry, 1963