Issue 6, 2013

Copper-mediated oxidative difluoromethylenation of aryl boronic acids with α-silyldifluoromethylphosphonates: a new method for aryldifluorophosphonates

Abstract

An unprecedented copper-mediated oxidative difluoromethylenation of aryl boronic acids with α-silyldifluoromethylphosphonates has been developed, allowing rapid access to a wide range of aryldifluorophosphonates containing various functional groups. This method provides a complementary and alternative method to Cu-mediated cross-couplings of aryl iodides with metalated difluoromethylphosphonates.

Graphical abstract: Copper-mediated oxidative difluoromethylenation of aryl boronic acids with α-silyldifluoromethylphosphonates: a new method for aryldifluorophosphonates

Supplementary files

Article information

Article type
Paper
Submitted
11 Jan 2013
Accepted
02 Mar 2013
First published
04 Mar 2013

New J. Chem., 2013,37, 1736-1741

Copper-mediated oxidative difluoromethylenation of aryl boronic acids with α-silyldifluoromethylphosphonates: a new method for aryldifluorophosphonates

X. Jiang, L. Chu and F. Qing, New J. Chem., 2013, 37, 1736 DOI: 10.1039/C3NJ00044C

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