Issue 94, 2013

An efficient method for the Heck–Catellani reaction of aryl halides

Abstract

We describe herein a new method that allows selective production of Catellani–Heck isomers from various aryl halides, including ones without ortho-groups. Under previous conditions, unhindered aryl halides were plagued with the formation of simple Heck isomers and multiple arylation and norbornene insertion. The use of a bulky PtBu3 ligand accelerates C–C reductive elimination from the key palladacycle.

Graphical abstract: An efficient method for the Heck–Catellani reaction of aryl halides

Supplementary files

Article information

Article type
Communication
Submitted
20 Aug 2013
Accepted
02 Oct 2013
First published
02 Oct 2013

Chem. Commun., 2013,49, 11035-11037

An efficient method for the Heck–Catellani reaction of aryl halides

X. Wu and J. (. Zhou, Chem. Commun., 2013, 49, 11035 DOI: 10.1039/C3CC46381H

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