Electronic effects in the acylation of .alpha.-chymotrypsin by para-substituted N-benzoylimidazoles
Author:
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi00308a021
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Nucleophilicities and Lewis basicities of imidazoles, benzimidazoles, and benzotriazoles;Organic & Biomolecular Chemistry;2010
2. Hydrolyses of N-Benzoyl-2-phenylimidazole and N-Benzoyl-4,5-diphenylimidazole;Journal of the Korean Chemical Society;2007-10-20
3. The Effect of the Leaving Group in the Acylation of α-Chymotrypsin byN-Acylimidazoles: The Reaction ofN-(3,3-Dimethylbutyryl)-4(5)-nitroimidazole;Bioorganic Chemistry;1998-10
4. Steric Effects in the Hydrolysis Reactions of N-Acylimidazoles. Effect of Aryl Substitution in the Leaving Group;The Journal of Organic Chemistry;1997-05-01
5. Kinetic and mechanistic effects of ease of carbon-nitrogen bond breaking in amide hydrolysis. The mechanisms of hydrolysis of N-acylimidazoles and N-acylbenzimidazoles;Accounts of Chemical Research;1993-06-01
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