Phosphine-Catalyzed Intermolecular Dienylation of Alkynoate with para-Quinone Methides

An interesting remote δ-C 1,6-addition and an isomerization cascade reaction for phosphine-catalyzed activated alkynes have been disclosed. The products featuring a functional diene and a 1,1-diaryl methyl motif have been obtained in moderate to good yields (30–86%) by applying para-quinone methides (p-QMs) and δ-substituted alkynoate with tributyl­phosphine (P n Bu3) catalysis, along with high regioselectivity and stereoselectivity (dr > 20:1). The wide scope of compatible substrates (35 examples), such as indolyl, oxindolyl, ester, and cinnamyl, expand the utility of this methodology. A plausible mechanism and some applications of it have also been presented.