Nad (P)+ - nad (P) H models. 67. stereospecific conversion of central chirality into axial chirality as a model for chemical evolution of a dehydrogenase
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Nad(P)+-nad(p)h models. 57
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
3. The R and S notations for this chirality were misused in a preceeding paper (ref. 3). The 9R-isomer described therein should be read as the 9S-isomer and vice versa.
4. Effets electroniques en stereochimie—II
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1. Enantioselective Synthesis of Atropisomers by Oxidative Aromatization with Central-to-Axial Conversion of Chirality;Molecules;2023-03-31
2. Stereoselection without Steric Effect but Controlled by Electronic Effect: Important Contribution of Ground State;Bulletin of the Chemical Society of Japan;1998-09
3. Stereospecificity observed in base-catalyzed electrochemical oxidation;Tetrahedron Letters;1991-03
4. NAD(P)H-NAD(P)+Models. 73. Structure-Stereochemistry Relationship in the Reaction of NAD Analog;Bulletin of the Chemical Society of Japan;1991-01
5. NAD(P)+-NAD(P)H Models. 72. Isotope Effects to Prove the Multi-Step Mechanism in the Reduction with an NAD(P)H Analog;Bulletin of the Chemical Society of Japan;1990-09
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