Issue 39, 2007

Consecutive palladium-catalyzed Hiyama–Heck reactions in aqueous media under ligand-free conditions

Abstract

Symmetric and asymmetric (E)-1,2-diarylethenes are synthesized from aryl bromides by consecutive one-pot Hiyama–Heck reactions carried out in water and under air; the only additives required are sodium hydroxide, palladium acetate and poly(ethylene glycol), and the products are isolable in many cases by simple filtration of the water solution.

Graphical abstract: Consecutive palladium-catalyzed Hiyama–Heck reactions in aqueous media under ligand-free conditions

Supplementary files

Article information

Article type
Communication
Submitted
21 May 2007
Accepted
03 Jul 2007
First published
25 Jul 2007

Chem. Commun., 2007, 4056-4058

Consecutive palladium-catalyzed Hiyama–Heck reactions in aqueous media under ligand-free conditions

Á. Gordillo, E. de Jesús and C. López-Mardomingo, Chem. Commun., 2007, 4056 DOI: 10.1039/B707583A

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