| Literature DB >> 29577534 |
Shenci Lu1, Jun-Yang Ong1,2, Si Bei Poh1, Terence Tsang1, Yu Zhao1,2.
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.Entities:
Keywords: N-heterocyclic carbenes; cycloaddition; decarboxylation; enantioselectivity; heterocycles
Year: 2018 PMID: 29577534 DOI: 10.1002/anie.201801340
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336