Issue 5, 2018

Photoredox 1,2-dicarbofunctionalization of unactivated alkenes via tandem radical difluoroalkylation and alkynyl migration

Abstract

Visible-light-mediated tandem radical difluoroalkylation and alkynylation of unactivated alkenes is described in this communication. The process comprises a mild C–C bond activation via intramolecular 1,4-alkynyl migration. The general and elegant protocol can serve as a straightforward access route to obtain a wide range of synthetically valuable difluoroalkylated linear alkynyl ketones under mild reaction conditions.

Graphical abstract: Photoredox 1,2-dicarbofunctionalization of unactivated alkenes via tandem radical difluoroalkylation and alkynyl migration

Supplementary files

Article information

Article type
Research Article
Submitted
07 Sep 2017
Accepted
03 Nov 2017
First published
06 Nov 2017

Org. Chem. Front., 2018,5, 797-800

Photoredox 1,2-dicarbofunctionalization of unactivated alkenes via tandem radical difluoroalkylation and alkynyl migration

J. Liu, W. Li, J. Xie and C. Zhu, Org. Chem. Front., 2018, 5, 797 DOI: 10.1039/C7QO00808B

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