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Issue 2, 2017
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The dual role of thiourea in the thiotrifluoromethylation of alkenes

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Abstract

Alkenes substituted with a thiourea undergo C–CF3 followed by intramolecular C–S bond formation with the Togni reagent and trifluoroacetic acid (TFA) at room temperature; thiols and thioamides are not suitable S-sources for this reaction. This anti-addition process involves a CF3 radical, and affords CF3-substituted thiazolines and thiazines for medicinal applications. A metal or photoredox catalyst is not required as the thiourea acts as a reductant, as well as serving as an S-source capable of adding to a C-centered radical. Mechanistic work comparing the reactivity of thiourea, urea, thioamide and thiol in the context of alkene trifluoromethylation demonstrates that in this series, the thiourea is unique for its ability to release CF3 radical from the Togni reagent, and to orchestrate trifluoromethylation followed by S-cyclization with both activated and unactivated alkenes.

Graphical abstract: The dual role of thiourea in the thiotrifluoromethylation of alkenes

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Supplementary files

Article information


Submitted
23 Jun 2016
Accepted
30 Sep 2016
First published
30 Sep 2016

This article is Open Access
All publication charges for this article have been paid for by the Royal Society of Chemistry

Chem. Sci., 2017,8, 1195-1199
Article type
Edge Article

The dual role of thiourea in the thiotrifluoromethylation of alkenes

P. Ricci, T. Khotavivattana, L. Pfeifer, M. Médebielle, J. R. Morphy and V. Gouverneur, Chem. Sci., 2017, 8, 1195
DOI: 10.1039/C6SC02790C

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