Chromatographic separation of the enantiomers of 2-carboalkoxyindolines and N-aryl-α-amino esters on chiral stationary phases derived from N-(3,5-dinitrobenzoyl)-α-amino acids-Reference-Cited by-同舟云学术

Chromatographic separation of the enantiomers of 2-carboalkoxyindolines and N-aryl-α-amino esters on chiral stationary phases derived from N-(3,5-dinitrobenzoyl)-α-amino acids

Published:1985-01 Issue: Volume:348 Page:89-96
ISSN:0021-9673
Container-title:Journal of Chromatography A
language:en
Short-container-title:Journal of Chromatography A

Author:

Pirkle William H.,Pochapsky Thomas C.,Mahler George S.,Field Richard E.

Publisher

Elsevier BV

Subject

Organic Chemistry,General Medicine,Biochemistry,Analytical Chemistry

Reference9 articles.

1. A widely useful chiral stationary phase for the high-performance liquid chromatography separation of enantiomers

2. A rational approach to the design of highly-effective chiral stationary phases

3. A rational approach to the design of highly effective chiral stationary phases for the liquid chromatographic separation of enantiomers

4. A chiral stationary phase for the facile resolution of amino acids, amino alcohols and amines as the N-3,5-dinitrobenzoyl derivatives

5. 73. Cyclic meso-ionic compounds. Part I. The structure of the sydnones and related compounds

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