Synthesis of Functionalized Benzofurans from para-Quinone Methides via Phospha-1,6-Addition/ O-Acylation/Wittig Pathway

Org Lett. 2019 Oct 4;21(19):8008-8012. doi: 10.1021/acs.orglett.9b03001. Epub 2019 Sep 19.

Abstract

An efficient synthesis of functionalized benzofurans is achieved under mild and metal-free conditions from stable para-quinone methides by treatment with phosphine, acyl chloride, and a base. This one-pot phospha-1,6-addition/O-acylation/Wittig reaction is also demonstrated under catalytic conditions with similar efficacy.

Publication types

  • Research Support, Non-U.S. Gov't