Issue 11, 2019

Electrochemical fluoromethylation triggered lactonizations of alkenes under semi-aqueous conditions

Abstract

An electrochemical difluoromethylation triggered lactonization of alkenes was developed for the first time. This protocol employs readily prepared CF2HSO2Na as the difluoromethylating reagent, affording unprecedented CF2H-containing lactones in moderate yields. Moreover, with CF3SO2Na as the trifluoromethylating reagent, a wide array of CF3-containing lactones were obtained under additional supporting electrolyte- and catalyst-free conditions.

Graphical abstract: Electrochemical fluoromethylation triggered lactonizations of alkenes under semi-aqueous conditions

Supplementary files

Article information

Article type
Edge Article
Submitted
08 Jan 2019
Accepted
14 Feb 2019
First published
14 Feb 2019
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2019,10, 3181-3185

Electrochemical fluoromethylation triggered lactonizations of alkenes under semi-aqueous conditions

S. Zhang, L. Li, J. Zhang, J. Zhang, M. Xue and K. Xu, Chem. Sci., 2019, 10, 3181 DOI: 10.1039/C9SC00100J

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