Chiral Primary Amine Catalyzed Asymmetric α‐Benzylation with In Situ Generated ortho‐Quinone Methides

Abstract

A dual activation strategy integrating primary amine catalysis and Lewis base activation has been developed for an asymmetric α-benzylation reaction. Enamines derived from β-ketocarbonyls could react effectively with in situ generated ortho-quinone methides under Lewis base activation in asymmetric α-benzylation of β-ketocarbonyls and α-branched aldehydes. The approach enables the creation of acyclic all-carbon quaternary stereocenters with excellent enantioselectivities and good activity.