Transition-Metal-Free Decarboxylative Propargylic Substitution/Cyclization with either Azolium Enolates or Acyl Anions

Angew Chem Int Ed Engl. 2018 May 14;57(20):5714-5719. doi: 10.1002/anie.201801340. Epub 2018 Apr 19.

Abstract

Presented herein is an unprecedented transition-metal-free propargylic substitution reaction with either azolium enolates or acyl anions, which are generated from aldehydes under N-heterocyclic carbene catalysis. This new catalytic activation operates on readily available cyclic propargylic carbamates through decarboxylation, and generates reactive allene intermediates that can undergo divergent cyclization pathways to deliver skeletally diverse polycyclic compounds with high levels of efficiency and excellent enantioselectivities.

Keywords: N-heterocyclic carbenes; cycloaddition; decarboxylation; enantioselectivity; heterocycles.

Publication types

  • Research Support, Non-U.S. Gov't