Issue 3, 2013

Carbofluorination via a palladium-catalyzed cascade reaction

Abstract

This article demonstrates the first examples of tandem C–C and C–F bond formation for the palladium-catalyzed carbofluorination of allenes. The intramolecular Heck-fluorination cascade provides monofluoromethylated heteroarenes, an important class of products in medicinal chemistry. We also describe an intermolecular variant for the three-component coupling of allenes, aryl iodides, and AgF. Mechanistic studies indicate that C–F bond formation occurs by outer sphere attack of fluoride on an allylpalladium fluoride intermediate.

Graphical abstract: Carbofluorination via a palladium-catalyzed cascade reaction

Supplementary files

Article information

Article type
Edge Article
Submitted
10 Dec 2012
Accepted
04 Jan 2013
First published
04 Jan 2013

Chem. Sci., 2013,4, 1216-1220

Carbofluorination via a palladium-catalyzed cascade reaction

M. Braun, M. H. Katcher and A. G. Doyle, Chem. Sci., 2013, 4, 1216 DOI: 10.1039/C2SC22198E

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