Article ID Journal Published Year Pages File Type
1314670 Journal of Fluorine Chemistry 2013 7 Pages PDF
Abstract

An efficient, ligand-free palladium-catalyzed method for the cross coupling reaction of pentafluorobenzene with phenols was developed. This reaction proceeds via a highly selective CF bond activation in the 3-position and is compatible with a variety of functional groups, delivering polyfluorinated aryl ethers in moderate to excellent yields.

Graphical abstractPalladium-based catalytic systems for cross coupling of pentafluorobenzene and phenols via highly selective CF bond activation in the 3-position have been established. The reactions exhibit good functional group compatibility and afford polyfluorinated aryl ethers in moderate to excellent yields.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► An efficient Pd-catalyzed method for synthesis of polyfluorinated diaryl ethers has been developed. ► This reaction proceeds with high chemo- and regioselectivity for the CF bond activation. ► A diverse set of important functional groups can be well tolerated in the protocol.

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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