Metal- and Hydride-Free Pentannulative Reductive Aldol Reaction.

Abstract

Traditionally, the reductive aldol reaction is a metal-catalyzed and hydride-promoted coupling between enones and aldehydes. We present a phosphine-mediated diastereoselective intramolecular reductive aldol reaction of α-substituted dienones and aldehydes, which is metal-free and hydride-free. The synthetic utility of the reductive aldol adducts is demonstrated by elaborating them in one step to indeno[1,2- b]furanones, indeno[1,2- b]pyrans, and dibenzo[ a, h]azulen-8-ones.