The stereochemical resolution of the enantiomers of aspartame on an immobilized ?-chymotrypsin hplc chiral stationary phase: The effect of mobile-phase composition and enzyme activity-Reference-Cited by-同舟云学术

The stereochemical resolution of the enantiomers of aspartame on an immobilized ?-chymotrypsin hplc chiral stationary phase: The effect of mobile-phase composition and enzyme activity

Published:1990 Issue:1 Volume:2 Page:32-37
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Jadaud Philippe,Wainer Irving W.

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference6 articles.

1. Enzymes as HPLC stationary phases for chiral resolutions: Initial investigations withα-chymotrypsin

2. The stereochemical resolution of enantiomeric free and derivatized amino acids using and hplc chiral stationary phase based on immobilized ?-chymotrypsin: Ciral separation due to solue structure or enzyme activity

3. Stereochemical recognition of enantiomeric and diastereomeric dipeptides by high-performance liquid chromatography on a chiral stationary phase based upon immobilized α-chymotrypsin

4. Stereochemical resolutions on an HPLC chiral stationary phase based upon ?-chymotrypsin: The effect of mobile phase composition and temperature on retention and stereoselectivity. Abstracts, Thirteenth Symposium on Column Liquid Chromatography, Stockholm, June, 1989 (in preparation).

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