Synthesis of a new family of four deoxycholic acid derived chiral stationary phases and their evaluation in the HPLC resolution of racemic compounds
Authors:
- A IulianoAIA Iuliano
- P SalvadoriPSP Salvadori
- G FélixGFG Félix
- 1 August 1999
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 10 (17) , 3353-3364
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Design, Synthesis, and Evaluation of Bile Acid-Based Molecular TweezersThe Journal of Organic Chemistry, 1996
- Chiral Discrimination on Polysaccharides DerivativesBulletin of the Chemical Society of Japan, 1995
- Evaluation of a chiral stationary phase based on mixed immobilized proteinsJournal of Chromatography A, 1994
- Axially dissymmetric bianthracene-based chiral stationary phase for the high-performance liquid chromatographic separation of enantiomersJournal of Chromatography A, 1994
- Evolution of chiral stationary phase design in the Pirkle laboratoriesJournal of Chromatography A, 1994
- Evaluation of a new polar—organic high-performance liquid chromatographic mobile phase for cyclodextrin-bonded chiral stationary phasesTrAC Trends in Analytical Chemistry, 1993
- An Improved Chiral Stationary Phase for the Chromatographic Separation of Underivatized Naproxen EnantiomersJournal of Liquid Chromatography, 1992
- Considerations of chiral recognition relevant to the liquid chromatography separation of enantiomersChemical Reviews, 1989
- Resolution of some β‐hydroxyphenethylamines as N‐(3,5‐dinitrobenzoyl) amides on chiral stationary phases derived from cinchona alkaloidsChirality, 1989
- High-performance liquid chromatography on chiral packed microbore columns with the 3,5-dinitrobenzoyl derivative of trans-1,2-diaminocyclohexane as selectorJournal of Chromatography A, 1988