6,6′-Dinitrobiphenyl-2,2′-dicarboxylic acid ionically bonded to aminopropyl silica: New axially chiral phase of C2 symmetry for high-performance liquid chromatographic separation of enantiomeric amino alcohol derivatives
- 1 April 1994
- journal article
- Published by Elsevier in Journal of Chromatography A
- Vol. 667 (1-2) , 11-17
- https://doi.org/10.1016/0021-9673(94)89046-3
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- High-performance liquid chromatographic separation of enantiomers on axially chiral binaphthalene dicarboxylic acid-chiral phenylethylamine bonded to silica gelJournal of Chromatography A, 1991
- C2 symmetry and asymmetric inductionChemical Reviews, 1989
- Considerations of chiral recognition relevant to the liquid chromatography separation of enantiomersChemical Reviews, 1989
- An Efficient Chiral Stationary Phase for High Performance Liquid Chromatographic Separation of Enantiomeric Aliphatic AlcoholsChemistry Letters, 1988
- High-performance liquid chromatographic separation of enantiomers on axially chiral binaphthalene derivatives bonded to silica gelJournal of Chromatography A, 1987
- Chromatographic separation of racemic amino acids by use of chiral crown ether-coated reversed-phase packingsJournal of Chromatography A, 1987
- Chiral separation of heterocyclic drugs by HPLC: solute-stationary phase base-pair interactionsJournal of the American Chemical Society, 1986
- Host-guest complexation. 14. Host covalently bound to polystyrene resin for chromatographic resolution of enantiomers of amino acid and ester saltsJournal of the American Chemical Society, 1979
- Host-guest complexation. 12. Total optical resolution of amine and amino ester salts by chromatographyJournal of the American Chemical Society, 1978
- Resolution of optical isomers by high-performance liquid chromatographyJournal of Chromatography A, 1978