Issue 19, 2016

Efficient photolytic C–H bond functionalization of alkylbenzene with hypervalent iodine(iii) reagent

Abstract

A practical approach to radical C–H bond functionalization by the photolysis of a hypervalent iodine(III) reagent is presented. The photolysis of [bis(trifluoroacetoxy)iodo]benzene (PIFA) leads to the generation of trifluoroacetoxy radicals, which allows the smooth transformation of various alkylbenzenes to the corresponding benzyl ester compounds under mild reaction conditions.

Graphical abstract: Efficient photolytic C–H bond functionalization of alkylbenzene with hypervalent iodine(iii) reagent

Supplementary files

Article information

Article type
Communication
Submitted
12 Sep 2015
Accepted
03 Dec 2015
First published
03 Dec 2015

Chem. Commun., 2016,52, 3758-3761

Author version available

Efficient photolytic C–H bond functionalization of alkylbenzene with hypervalent iodine(III) reagent

R. Sakamoto, T. Inada, S. Selvakumar, S. A. Moteki and K. Maruoka, Chem. Commun., 2016, 52, 3758 DOI: 10.1039/C5CC07647A

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