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Issue 32, 2012
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Pd(OAc)2 without added ligand as an active catalyst for Mizoroki–Heck reaction in aqueous media

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Abstract

Conditions for an efficient ligand-free Heck C–C coupling reaction of aryl iodides and bromides with terminal olefins under aerobic conditions have been developed. Critical to the success of this new protocol is the use of palladium acetate as an extremely active catalyst for the Heck reaction in water and aqueous media. Both the base and the solvent were found to have a fundamental influence on the efficiency of the reaction, with K2CO3 and a mixture of (2 : 1) H2O/DMSO being the optimal base and solvent, respectively.

Graphical abstract: Pd(OAc)2 without added ligand as an active catalyst for Mizoroki–Heck reaction in aqueous media

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Supplementary files

Article information


Submitted
10 May 2012
Accepted
30 Sep 2012
First published
04 Oct 2012

RSC Adv., 2012,2, 12091-12095
Article type
Communication

Pd(OAc)2 without added ligand as an active catalyst for Mizoroki–Heck reaction in aqueous media

M. Amini, M. Bagherzadeh, Z. Moradi-Shoeili and D. M. Boghaei, RSC Adv., 2012, 2, 12091
DOI: 10.1039/C2RA21459H

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