Highly enantioselective copper-catalyzed propargylic amination to access N-tethered 1,6-enynes

RSC Adv. 2020 Oct 20;10(63):38478-38483. doi: 10.1039/d0ra07698h. eCollection 2020 Oct 15.

Abstract

A highly enantioselective copper-catalyzed propargylic amination starting from benzylic allylic amines has been developed with a new chiral N,N,P ligand. A series of N-tethered 1,6-enynes were synthesized in good to excellent yields with excellent enantioselectivities. Utilization of transition metal-catalyzed cycloisomerization of 1,6-enynes provides several enantioselectively enriched chiral five-membered N-heterocycles efficiently.