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
- 30 January 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (6) , 1186-1192
- https://doi.org/10.1021/ja972804t
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- NAD(P)+–NAD(P)H models. 84. Stereochemistry controlled by the electronic effect from a sulfinyl groupHeteroatom Chemistry, 1995
- 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 AnalogsJournal of the American Chemical Society, 1994
- Enthalpy of steric inhibition to solvation due to tert-butyl groups on an anion radicalJournal of the American Chemical Society, 1981
- pH Variation of isotope effects in enzyme-catalyzed reactions. 2. Isotope-dependent step not pH dependent. Kinetic mechanism of alcohol dehydrogenaseBiochemistry, 1981
- New membrane carrier for selective transport of metal ionsJournal of the American Chemical Society, 1980
- Comparison of the structures of enzymic and nonenzymic transition states. Reductive desulfonation of 4-X-2,6-dinitrobenzene sulfonates by reduced nicotinamide adenine dinucleotideBiochemistry, 1977
- Models for NADH coenzymes. Isotope effects in the N-benzyldihydronicotinamide/N-benzylnicotinamide salt transhydrogenation reactionJournal of the American Chemical Society, 1977
- Hydride transfer reactions. Oxidation of N-methylacridan by 1,4-benzoquinone and related .pi. acceptorsJournal of the American Chemical Society, 1976
- The Thermal Racemization of Dimethyl (-)-BromosuccinateJournal of the American Chemical Society, 1952
- 2. über die Einwirkung von Ammoniak und Aminbasen auf gechlorte ChinoneEuropean Journal of Organic Chemistry, 1881