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

高对映选择性铜催化炔丙基胺化反应合成N-连接的1,6-烯炔

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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.

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