Issue 12, 2018

Ruthenium(ii)-catalyzed α-fluoroalkenylation of arenes via C–H bond activation and C–F bond cleavage

Abstract

Ru(II)-Catalyzed efficient α-fluoroalkenylation of arenes has been realized with gem-difluorostyrene as an olefinating reagent. This coupling system is efficient with a broad substrate scope, providing 1,2-diaryl-substituted monofluoroalkenes with good to excellent regio- and stereoselectivities under silver-free conditions.

Graphical abstract: Ruthenium(ii)-catalyzed α-fluoroalkenylation of arenes via C–H bond activation and C–F bond cleavage

Supplementary files

Article information

Article type
Research Article
Submitted
19 Mar 2018
Accepted
04 May 2018
First published
07 May 2018

Org. Chem. Front., 2018,5, 1978-1982

Ruthenium(II)-catalyzed α-fluoroalkenylation of arenes via C–H bond activation and C–F bond cleavage

N. Li, J. Chang, L. Kong and X. Li, Org. Chem. Front., 2018, 5, 1978 DOI: 10.1039/C8QO00297E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements