Stereospecificity observed in base-catalyzed electrochemical oxidation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
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2. NAD(P)+-NAD(P)H models. 61. An interconversion between central and axial chiralities as evidence for a functional model of chemical evolution of an enzyme
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1. Enantioselective Synthesis of Atropisomers by Oxidative Aromatization with Central-to-Axial Conversion of Chirality;Molecules;2023-03-31
2. Electrochemistry ofNAD(P)+/NAD(P)H;Encyclopedia of Electrochemistry;2002-08-27
3. NAD(P)+−NAD(P)H Models. 90. Stereoselection Controlled by Electronic Effect of a Carbonyl Group in Oxidation of NAD(P)H Analog;The Journal of Organic Chemistry;2000-09-13
4. Stereoselection without Steric Effect but Controlled by Electronic Effect: Important Contribution of Ground State;Bulletin of the Chemical Society of Japan;1998-09
5. NAD(P)+-NAD(P)H Models. 88. Stereoselection without Steric Effect but Controlled by Electronic Effect of a Carbonyl Group: Syn/Anti Reactivity Ratio, Kinetic Isotope Effect, and an Electron-Transfer Complex as a Reaction Intermediate;Journal of the American Chemical Society;1998-01-30
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