NAD(P)+–NAD(P)H models. 84. Stereochemistry controlled by the electronic effect from a sulfinyl group
- 1 January 1995
- journal article
- Published by Wiley in Heteroatom Chemistry
- Vol. 6 (1) , 51-56
- https://doi.org/10.1002/hc.520060112
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- 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
- Further evidence to understand the stereochemistry of the reactions of α‐sulfinyl carbanionsHeteroatom Chemistry, 1992
- ortho-Sulfenylation ofN,N-Dimethyl-1-phenylethylamine and Oxidation of the Resultant SulfidesSynthesis, 1992
- Stereochemistry in the reaction of alkylsulfinyl phenylmethyl carbanion with electrophilesHeteroatom Chemistry, 1990
- t-Butylsulfinyl Phenylmethyl Carbanion. Conformation in Nonpolar SolventBulletin of the Chemical Society of Japan, 1988
- Stereochemistry of the .alpha.-sulfinyl phenylmethyl carbanion. Reevaluation of the configurationThe Journal of Organic Chemistry, 1987
- 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 enzymeJournal of the American Chemical Society, 1986
- Regio- and stereo-selective hydride uptake in model systems related to 3-carbamoyl pyridinium compoundsJournal of the Chemical Society, Chemical Communications, 1985
- Stereospecific alkylation of a carbanion in the solid stateJournal of the American Chemical Society, 1980
- Concerning the absolute configuration of proton exchange at a prochiral centre in sulphoxidesJournal of the Chemical Society D: Chemical Communications, 1969