Normal acid behavior for C(α)-proton transfer from a thiazolium lon
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry
Reference50 articles.
1. Intrinsic barriers of reactions and the principle of nonperfect synchronization
2. Ionic intermediates in enzyme-catalyzed carbon-carbon bond formation: patterns, prototypes, probes, and proposals
3. Thiazolium C(2)-proton exchange: structure-reactivity correlations and the pKa of thiamin C(2)-H revisited
4. Thiazolium C(2)-proton exchange: general-base catalysis, direct proton transfer, and acid inhibition
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3. Proton Transfer from the C5-proR/proS Positions of l-Dihydroorotate: General-Base Catalysis, Isotope Effects, and Internal Return1;Journal of the American Chemical Society;1999-12-01
4. Normal acid/base behaviour in proton transfer reactions to alkoxy substituted carbenes: estimates for intrinsic barriers to reaction and pK(a) values;CAN J CHEM;1999
5. Kinetics of C(2α)-Proton Abstraction from 2-Benzylthiazolium Salts Leading to Enamines Relevant to Catalysis by Thiamin-Dependent Enzymes;Journal of the American Chemical Society;1997-03-01
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