Journal of the American Chemical Society, Vol.131, No.38, 13588-13588, 2009
Sodium Tetraarylborates as Effective Nucleophiles in Rhodium/Diene-Catalyzed 1,4-Addition to beta,beta-Disubstituted alpha,beta-Unsaturated Ketones: Catalytic Asymmetric Construction of Quaternary Carbon Stereocenters
A rhodium-catalyzed 1,4-addition of sodium tetraarylborates to beta,beta-disubstituted alpha,beta-unsaturated ketones is described. Highly efficient asymmetric catalysis has also been achieved by employing a readily available chiral diene ligand, leading to the construction of quaternary carbon stereocenters with high enantioselectivity.