Issue 74, 2019

Visible-light-mediated defluorinative cross-coupling of gem-difluoroalkenes with thiols

Abstract

Here we report a visible-light-mediated monofluoroalkenylation through defluorinative cross-coupling of gem-difluoroalkenes with aryl, benzyl, and alkyl thiols. This novel strategy provides facile and efficient access to tri/tetra-substituted monofluoroalkenes under mild reaction conditions with good functional group tolerance. Late-stage modification of natural products indicated the synthetic potential of this S–H monofluoroalkenylation process.

Graphical abstract: Visible-light-mediated defluorinative cross-coupling of gem-difluoroalkenes with thiols

Supplementary files

Article information

Article type
Communication
Submitted
10 Jul 2019
Accepted
20 Aug 2019
First published
20 Aug 2019

Chem. Commun., 2019,55, 11103-11106

Visible-light-mediated defluorinative cross-coupling of gem-difluoroalkenes with thiols

J. Wang, B. Huang, C. Yang and W. Xia, Chem. Commun., 2019, 55, 11103 DOI: 10.1039/C9CC05293C

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