High-performance liquid chromatographic separation of enantiomers on axially chiral binaphthalene dicarboxylic acid-chiral phenylethylamine bonded to silica gel
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry
Reference13 articles.
1. Useful and easily prepared chiral stationary phases for the direct chromatographic separation of the enantiomers of a variety of derivatized amines, amino acids, alcohols, and related compounds
2. Enantiomer Separation by HPLC with Some Urea Derivatives of L-Valine as Novel Chiral Stationary Phases
3. High-performance liquid chromatographic separation of enantiomers on (1R,3R)-trans-chrysanthemic acid and its amide derivatives bonded to silica gel
4. High-performance liquid chromatographic separation of enantiomers on (S)-1 -(α-naphthyl)ethylamine bonded to silica gel
5. High-performance liquid chromatographic separation of chiral alcohols on chiral stationary phases
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1. Optical resolution of some racemates by HPLC using chiral polymers having (+)-5-oxobornyl moieties;Journal of Applied Polymer Science;1999-05-02
2. Synthesis and polymerization of 3‐oxobornyl methacrylate;Journal of Applied Polymer Science;1996-08-15
3. HPLC separation of the enantiomers of racemic benzergoline derivatives on a chiral binaphthalene covalently bonded to silica gel;Journal of High Resolution Chromatography;1995-04
4. Axially dissymmetric bianthracene-based chiral stationary phase for the high-performance liquid chromatographic separation of enantiomers;Journal of Chromatography A;1994-09
5. 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;Journal of Chromatography A;1994-04
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