NAD(P)+–NAD(P)H Models. 81. Temperature-Dependent Stereospecificity in the Interconversion between Central and Axial Chiralities
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/66/4/66_4_1191/_pdf
Reference19 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. NAD(P)H-NAD(P)+Models. 73. Structure-Stereochemistry Relationship in the Reaction of NAD Analog
4. NAD (P)+-NAD (P)H Models. 69. Mechanism of Stereospecific (NET) Hydride Transfer Controlled by Electronic Effect
5. NAD(P)H-NAD(P)+Models. 74. Entropy-Controlled Kinetics, Stereochemistry, and Tunneling Effect
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1. Hydride Reduction of NAD(P)+ Model Compounds with a Ru(II)–Hydrido Complex;Organometallics;2015-11-20
2. Consideration of molecular arrangements in regio- and enantioselective reduction of an NAD model compound controlled by carbonyl oxygen orientation;Organic & Biomolecular Chemistry;2007
3. Unusual Temperature Dependence of Enantioselectivity in Asymmetric Reductions by Chiral NADH Models;Organic Letters;2006-04-21
4. NAD/NADH Models with Axial/Central Chiralities: Superiority of the Quinoline Ring System;The Journal of Organic Chemistry;2001-02-08
5. 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
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