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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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Publication details

The article was received on 23 Jun 2016, accepted on 30 Sep 2016 and first published on 30 Sep 2016


Article type: Edge Article
DOI: 10.1039/C6SC02790C
Citation: Chem. Sci., 2017,8, 1195-1199
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    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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