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Synlett 2019; 30(09): 1008-1014
DOI: 10.1055/s-0037-1612214
DOI: 10.1055/s-0037-1612214
synpacts
Enantioselective Reductive Diarylation of Alkenes by Ni-Catalyzed Domino Heck Cyclization/Cross Coupling
We acknowledge financial support from the ‘1000-Youth Talents Plan’, National Natural Science Foundation of China (No. 21702149) and Fundamental Research Funds for the Central Universities (2042018kf0012).Further Information
Publication History
Received: 19 December 2018
Accepted after revision: 21 January 2019
Publication Date:
18 February 2019 (online)
Abstract
A Ni-catalyzed enantioselective reductive diarylation of alkenes through a tandem Heck cyclization/cross coupling of two structurally distinguished aryl bromides is accomplished for the first time. This reaction takes place under very mild conditions with high efficiency and tolerates a variety of functional groups. Thus, it provides a rapid access to various medicinally relevant bis-heterocycles containing all-carbon quaternary centers with very high enantioselectivity.
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