NAD(P)+–NAD(P)H Models. 86. Nonsteric Stereochemistry in Hydride-Transfer to Sulfinylpyridinium Ion
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj/69/4/69_4_1093/_pdf
Reference23 articles.
1. 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
2. NAD(P)+-NAD(P)H models. 84. Stereochemistry controlled by the electronic effect from a sulfinyl group
3. NAD(P)+-NAD(P)H models. 66. Stereospecific interconversion between different chiralities in the reduction of a quinolinium salt
4. Theoretical studies on the hydride transfer between 1-methyl-1,4-dihydronicotinamide and its corresponding pyridinium salt
5. Reactivity of biologically important reduced pyridines
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1. Consideration of molecular arrangements in regio- and enantioselective reduction of an NAD model compound controlled by carbonyl oxygen orientation;Organic & Biomolecular Chemistry;2007
2. Carbonyl Orientation Determines Regio- and Enantioselectivity in 1,2-/1,4-Reduction of an NAD Model Compound;Organic Letters;2004-07-23
3. Stereoselection without Steric Effect but Controlled by Electronic Effect: Important Contribution of Ground State;Bulletin of the Chemical Society of Japan;1998-09
4. 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
5. Rational de novo design of NADH mimic for stereoselective reduction based on molecular orbital calculation;Tetrahedron;1998-01
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