The Effect of the Leaving Group in the Acylation of α-Chymotrypsin byN-Acylimidazoles: The Reaction ofN-(3,3-Dimethylbutyryl)-4(5)-nitroimidazole
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry
Reference47 articles.
1. The Current Status of the α-Chymotrypsin Mechanism
2. The Formation of an Acyl-enzyme Intermediate in the α-Chymotrypsin-catalyzed Hydrolyses of Non-labile trans-Cinnamic Acid Esters1-3
3. The Kinetic Consequences of the Acyl-Enzyme Mechanism for the Reactions of Specific Substrates with Chymotrypsin
4. Kinetic Evidence for the Formation of Acyl-Enzyme Intermediates in the α-Chymotrypsin-Catalyzed Hydrolyses of Specific Substrates
5. The Observation of Acyl-Enzyme Intermediates in the α-Chymotrypsin-Catalyzed Reactions of N-Acetyl-L-tryptophan Derivatives at Low pH
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1. Kinetic resolution of (R,S)-pyrazolides containing substituents in the leaving pyrazole for increased lipase enantioselectivity;Journal of Molecular Catalysis B: Enzymatic;2010-09
2. (R,S)-Azolides as Novel Substrates for Lipase-Catalyzed Hydrolytic Resolution in Organic Solvents;Advanced Synthesis & Catalysis;2009-10
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