Origin of Enantioreversal in the Rhodium-Catalyzed Asymmetric Hydrogenation of Prochiral Enamides and the Effect of the α-Substituent
journal contributionposted on 03.05.2001, 00:00 by Steven Feldgus, Clark R. Landis
The enantioselectivity of prochiral enamide hydrogenation depends on the structure of the enamide, with particular sensitivity to the nature of the α-substituent. Recently, Burk has reported a spectacular example of structure sensitivity for [Rh(DuPHOS)]+-catalyzed enamide hydrogenations: although enamides containing either carboxyl or tert-butyl α-substituents hydrogenate to ≥99% enantiomeric excess, the sense of enantioselection for the two substrate classes is reversed. Why should the magnitude and sense of enantioselectivity depend so strongly on the enamide α-substituent? We report the application of QM/MM (ONIOM) computations to address this long-standing issue in asymmetric catalysis. Specifically, we demonstrate that computational methods reproduce the α-substituent effect in enamide hydrogenation catalysis and probe how the interaction of the enamide CC bond and the catalyst varies with the structure of the substrate. The picture that emerges emphasizes the complex confluence of both electronic effects (i.e., those effects that do not depend on the size of the model system) and steric effects in controlling the stereochemistry of enamide hydrogenation reactions.