A Mechanochemical Switch to Control Radical Intermediates
Author:
Affiliation:
1. Laboratory of Computational Chemistry and Biochemistry, EPFL, Lausanne, Switzerland 1015
2. Indiana University-Purdue University, Indianapolis, Indiana 46202, United States
Funder
Swiss National Science Foundation
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi500050k
Reference55 articles.
1. Enzymic Reaction Selectivity by Negative Catalysis or How Do Enzymes Deal with Highly Reactive Intermediates?
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3. Thermolysis of the cobalt-carbon bond of adenosylcobalamin. 2. Products, kinetics, and cobalt-carbon bond dissociation energy in aqueous solution
4. Thermolysis of the cobalt-carbon bond in adenosylcorrins. 3. Quantification of the axial base effect in adenosylcobalamin by the synthesis and thermolysis of axial base-free adenosylcobinamide. Insights into the energetics of enzyme-assisted cobalt-carbon bond homolysis
5. Tyrosine 89 Accelerates Co−Carbon Bond Homolysis in Methylmalonyl-CoA Mutase
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