Anionic Four-Electron Donor-Based
Palladacycles as Catalysts for Addition
Reactions of Arylboronic Acids with
α,β-Unsaturated Ketones, Aldehydes,
and α-Ketoesters
Anionic four-electron donor-based palladacycle-catalyzed 1,4-additions of arylboronic acids with α,β-unsaturated ketones and 1,2-additions of
arylboronic acids with aldehydes and α-ketoesters are described. Our study demonstrated that palladacycles were highly efficient, practical
catalysts for these addition reactions. The work described here not only opened a new paradigm for the application of palladacycles, but may
also pave the road for other metalacycles as practically useful catalysts for such addition reactions including asymmetric ones