Issue 6, 2020

Copper-catalyzed enantioselective arylalkynylation of alkenes

Abstract

A copper-catalyzed enantioselective arylalkynylation of alkenes with diaryliodonium salt and a monosubstituted alkyne is reported. The three-component coupling reactions proceed under mild reaction conditions with a broad substrate scope, leading to synthetically valuable 1,2-diaryl-3-butynes. The key to the success of this chemistry is the employment of the chiral bisoxazoline-phenylaniline (BOPA) ligand. A novel reaction pathway involving the phenyl radical generation under thermal copper catalysis is proposed according to mechanistic studies.

Graphical abstract: Copper-catalyzed enantioselective arylalkynylation of alkenes

Supplementary files

Article information

Article type
Edge Article
Submitted
13 Aug 2019
Accepted
26 Nov 2019
First published
08 Jan 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2020,11, 1623-1628

Copper-catalyzed enantioselective arylalkynylation of alkenes

G. Lei, H. Zhang, B. Chen, M. Xu and G. Zhang, Chem. Sci., 2020, 11, 1623 DOI: 10.1039/C9SC04029C

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