NAD(P)+-NAD(P)H models. 84. Stereochemistry controlled by the electronic effect from a sulfinyl group
Author:
Publisher
Wiley
Subject
General Chemistry
Reference23 articles.
1. NAD(P)+-NAD(P)H models. 66. Stereospecific interconversion between different chiralities in the reduction of a quinolinium salt
2. J. Chem. Soc., Chem. Commun., 1985, 1009.
3. NAD(P+/NAD(P)H Models. 83. Molecular Asymmetry with a Carbonyl Group: Electronically Controlled Stereochemistry in the Reaction of NAD(P)+/NAD(P)H Analogs
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1. Stereoselection without Steric Effect but Controlled by Electronic Effect: Important Contribution of Ground State;Bulletin of the Chemical Society of Japan;1998-09
2. 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
3. Stereospecific Redox Reaction Directed by a Sulfinyl Group;Phosphorus, Sulfur, and Silicon and the Related Elements;1997-01-01
4. NAD(P)+–NAD(P)H Models. 86. Nonsteric Stereochemistry in Hydride-Transfer to Sulfinylpyridinium Ion;Bulletin of the Chemical Society of Japan;1996-04
5. Non-steric stereochemistry solely controlled by orientation of dipolar function;Journal of Physical Organic Chemistry;1995-09
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