Issue 8, 2022

Copper-catalyzed ortho-alkenylation of quinoline N-oxides with alkynes

Abstract

A copper-catalyzed regioselective C-2 alkenylation of quinoline N-oxides with alkynes and pinacol diborane has been developed. This method provides efficient access to a wide variety of deoxygenated 2-alkenyl quinolines with good functional group tolerance. In particular, highly regio- and stereoselective reactions were observed with unsymmetrical alkynes such as aryl(alkyl)acetylenes and enynes. The reaction involves borylcupration of alkynes, capture of the catalytically generated alkenyl copper species by quinoline N-oxides and deborylation.

Graphical abstract: Copper-catalyzed ortho-alkenylation of quinoline N-oxides with alkynes

Supplementary files

Article information

Article type
Research Article
Submitted
03 Dec 2021
Accepted
05 Mar 2022
First published
09 Mar 2022

Org. Chem. Front., 2022,9, 2198-2203

Copper-catalyzed ortho-alkenylation of quinoline N-oxides with alkynes

L. Jiang, H. Hu and Y. Liu, Org. Chem. Front., 2022, 9, 2198 DOI: 10.1039/D1QO01800K

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