Origin of the Enantioselectivity in the Hydrogen Transfer Reduction of Carbonyls by a Rhodium(I) Complex: A Theoretical Study
- 1 May 2001
- journal article
- Published by American Chemical Society (ACS) in Organometallics
- Vol. 20 (11) , 2207-2214
- https://doi.org/10.1021/om010120v
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Catalytic Asymmetric Hydride Transfer Reduction of Ketones with Rhodium and Chiral Diamine Ligands: Approach of the Active Species Structure by DFT CalculationsOrganometallics, 2000
- Hydride Transfer Reduction of Carbonyls by a Rhodium(I) Complex: A Theoretical Study. 1. The Two-Step MechanismOrganometallics, 2000
- Ru(arene)(amino alcohol)-Catalyzed Transfer Hydrogenation of Ketones: Mechanism and Origin of EnantioselectivityJournal of the American Chemical Society, 1999
- Structure of the Diamine−Rh(I) Precursor in the Asymmetric Hydride Transfer Reduction of Ketones: A Theoretical and Experimental ApproachJournal of the American Chemical Society, 1998
- Asymmetric Transfer Hydrogenation Catalyzed by Chiral Ruthenium ComplexesAccounts of Chemical Research, 1997
- Single-electron transfer, a major reaction pathway in organic chemistry. An answer to recent criticismsAccounts of Chemical Research, 1988
- Extended gaussian-type valence basis sets for calculations involving non-empirical core pseudopotentialsMolecular Physics, 1988
- Density-functional exchange-energy approximation with correct asymptotic behaviorPhysical Review A, 1988
- Ab initio effective core potentials for molecular calculations. Potentials for K to Au including the outermost core orbitalsThe Journal of Chemical Physics, 1985
- Quininone1Journal of the American Chemical Society, 1945