Issue 23, 2016

Silver-initiated radical ring expansion/fluorination of ethynyl cyclobutanols: efficient synthesis of monofluoroethenyl cyclopentanones

Abstract

A stereoselective synthesis of β-halogenated 2-methylenecyclopentanones via silver-catalyzed formal ring expansion using water as the cosolvent is described. A variety of 2-methylenecyclopentanones with fluoro, chloro and bromo functionalities are efficiently prepared from 1-alkynyl cyclobutanols. This method offers facile access to halogenated complex molecules which are not only useful chemicals but also valuable building blocks for further derivatizations.

Graphical abstract: Silver-initiated radical ring expansion/fluorination of ethynyl cyclobutanols: efficient synthesis of monofluoroethenyl cyclopentanones

Supplementary files

Article information

Article type
Communication
Submitted
23 Sep 2016
Accepted
17 Oct 2016
First published
18 Oct 2016

Green Chem., 2016,18, 6236-6240

Silver-initiated radical ring expansion/fluorination of ethynyl cyclobutanols: efficient synthesis of monofluoroethenyl cyclopentanones

Q. Tian, B. Chen and G. Zhang, Green Chem., 2016, 18, 6236 DOI: 10.1039/C6GC02656G

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