Issue 11, 2011

Fluoride catalyzed P–aryl-coupling—a mild approach to functionalized arylphosphines

Abstract

Functionalized triaryl- and diarylalkylphosphines are accessible in high yields following a mild fluoride catalyzed phosphorous–carbon coupling protocol starting from fluoroarenes and silylated phosphines. The reaction requires a minimum of solvent and can be applied to the synthesis of several functionalized phosphines on a kilogram scale without problems. In contrast to the phosphine synthesis in a superbasic medium, there is no salt formation during the reaction which simplifies the work-up process.

Graphical abstract: Fluoride catalyzed P–aryl-coupling—a mild approach to functionalized arylphosphines

Supplementary files

Article information

Article type
Paper
Submitted
27 May 2011
Accepted
11 Jul 2011
First published
08 Aug 2011

New J. Chem., 2011,35, 2488-2495

Fluoride catalyzed P–aryl-coupling—a mild approach to functionalized arylphosphines

A. Reis, D. Dehe, S. Farsadpour, I. Munstein, Y. Sun and W. R. Thiel, New J. Chem., 2011, 35, 2488 DOI: 10.1039/C1NJ20448C

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