Issue 30, 2014

Iron-catalyzed radical aryldifluoromethylation of activated alkenes to difluoromethylated oxindoles

Abstract

An iron-catalyzed aryldifluoromethylation of activated alkenes under mild reaction conditions has been developed, which is a rare example where a cosolvent is used to improve the reaction yield along with Fenton's reagent and thus provides an economic and green method for the synthesis of a variety of difluoromethylated oxindoles. Preliminary mechanistic investigations indicate a radical addition path.

Graphical abstract: Iron-catalyzed radical aryldifluoromethylation of activated alkenes to difluoromethylated oxindoles

Supplementary files

Article information

Article type
Communication
Submitted
10 Apr 2014
Accepted
30 May 2014
First published
03 Jun 2014

Org. Biomol. Chem., 2014,12, 5582-5585

Author version available

Iron-catalyzed radical aryldifluoromethylation of activated alkenes to difluoromethylated oxindoles

J. Wang, X. Zhang, Y. Bao, Y. Xu, X. Cheng and X. Wang, Org. Biomol. Chem., 2014, 12, 5582 DOI: 10.1039/C4OB00758A

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