Issue 11, 2015

A new method for the synthesis of difluoromethyl enol ethers by O-difluoromethylation of 1,3-diones with ClCF2CO2Et

Abstract

A facile, efficient, single-step protocol for the synthesis of difluoromethyl enol ether derivatives by O-difluoromethylation of 1,3-diones via in situ generation of difluorocarbene from ClCF2CO2Et has been developed. The functional group tolerance, scalability of the reaction, and mild reaction conditions make it an attractive protocol for the synthesis of biologically relevant difluoromethyl ethers of interest to the pharmaceutical and agrochemical industries.

Graphical abstract: A new method for the synthesis of difluoromethyl enol ethers by O-difluoromethylation of 1,3-diones with ClCF2CO2Et

Supplementary files

Article information

Article type
Paper
Submitted
06 Jan 2015
Accepted
27 Jan 2015
First published
27 Jan 2015

Org. Biomol. Chem., 2015,13, 3432-3437

A new method for the synthesis of difluoromethyl enol ethers by O-difluoromethylation of 1,3-diones with ClCF2CO2Et

X. Lin and Z. Weng, Org. Biomol. Chem., 2015, 13, 3432 DOI: 10.1039/C5OB00020C

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