Issue 37, 2015

Pd-catalyzed carbonylative access to aroyl phosphonates from (hetero)aryl bromides

Abstract

The first transition-metal catalysed carbonylation with a phosphorus nucleophile is presented. This transformation provides efficient and mild access to aroylphosphonates under mild conditions, thus ensuring a broad substrate scope. The utility of aroylphosphonates as useful reagents, capable of participating in a number of transformations, is subsequently demonstrated. Furthermore, access to [13C]-carbonyl labelled aroylphosphonates is easily realised for the first time, as only a near stoichiometric amount of CO is required applying this carbonylation.

Graphical abstract: Pd-catalyzed carbonylative access to aroyl phosphonates from (hetero)aryl bromides

Supplementary files

Article information

Article type
Communication
Submitted
11 Mar 2015
Accepted
01 Apr 2015
First published
01 Apr 2015

Chem. Commun., 2015,51, 7831-7834

Author version available

Pd-catalyzed carbonylative access to aroyl phosphonates from (hetero)aryl bromides

Z. Lian, H. Yin, S. D. Friis and T. Skrydstrup, Chem. Commun., 2015, 51, 7831 DOI: 10.1039/C5CC02085A

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