Issue 9, 2017

Sunlight decatungstate photoinduced trifluoromethylations of (hetero)aromatics and electron-poor olefins

Abstract

Tetrabutylammonium decatungstate has been exploited to photoinduce the trifluoromethylation of (hetero)aromatics and electron-poor olefins. The process made use of the cheap Langlois’ reagent (CF3SO2Na) and occurred under sunlight irradiation in an acetonitrile/water mixture. The trifluoromethylation of (hetero)aromatics required the use of potassium persulfate as an additive and the mono- or bis-trifluoromethylated adducts were obtained, depending on the actual reaction conditions and the chosen substrate.

Graphical abstract: Sunlight decatungstate photoinduced trifluoromethylations of (hetero)aromatics and electron-poor olefins

Supplementary files

Article information

Article type
Communication
Submitted
17 May 2017
Accepted
26 Jul 2017
First published
27 Jul 2017

Photochem. Photobiol. Sci., 2017,16, 1375-1380

Sunlight decatungstate photoinduced trifluoromethylations of (hetero)aromatics and electron-poor olefins

S. Corsico, M. Fagnoni and D. Ravelli, Photochem. Photobiol. Sci., 2017, 16, 1375 DOI: 10.1039/C7PP00179G

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.

Spotlight

Advertisements