Preparation of the optical isomers of arginine, histidine and S-benzylcysteine by asymmetric enzymatic hydrolysis of their acetyl derivatives
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry,Biophysics
Reference19 articles.
1. PREPARATION OF l- AND d-ALANINE BY ENZYMATIC RESOLUTION OF ACETYL-dl-ALANINE
2. THE RESOLUTION OF SEVERAL RACEMIC AMINO ACIDS
3. RESOLUTION OF RACEMIC PHENYLALANINE, TYROSINE, AND TRYPTOPHAN
4. ENZYMATIC RESOLUTION OF RACEMIC LYSINE, NORLEUCINE, NORVALINE, AND α-AMINOBUTYRIC ACID
5. CONFIGURATION OF ISOMERIC ALLOTHREONINES BY ENZYMATIC RESOLUTION
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1. Synthesis of [1,1′ -13C2]-L-cystine;Journal of Labelled Compounds and Radiopharmaceuticals;1991-08
2. The stereochemistry of the enzymic decarboxylation of L-arginine and of L-ornithine;Canadian Journal of Chemistry;1982-11-15
3. Studies of enzyme-mediated reactions. Part 13. Stereochemical course of the formation of histamine by decarboxylation of (2S)-histidine with enzymes from Clostridium welchii and Lactobacillus 30a;Journal of the Chemical Society, Perkin Transactions 1;1980
4. Structure of nitroarginine. A nitrogen-15 nuclear magnetic resonance study;The Journal of Organic Chemistry;1979-01
5. Studies on the Catalytic Action of Poly-α-amino Acids;The Journal of Biochemistry;1977-01
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