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Molecules 2015, 20(5), 7528-7557;

Recent Developments in the Suzuki-Miyaura Reaction: 2010–2014

Department of Chemistry, University of Sussex, Brighton BN1 9QJ, UK
Author to whom correspondence should be addressed.
Academic Editor: John Spencer
Received: 17 March 2015 / Revised: 10 April 2015 / Accepted: 13 April 2015 / Published: 24 April 2015
(This article belongs to the Special Issue Recent Advances in Boron Chemistry)
Full-Text   |   PDF [1191 KB, uploaded 24 April 2015]   |  


The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic halide or pseudo-halide in the presence of a palladium or nickel catalyst and a base, has arguably become one of most utilized tools for the construction of a C-C bond. This review intends to be general account of all types of catalytic systems, new coupling partners and applications, including the literature between September 2010 and December 2014. View Full-Text
Keywords: Suzuki-Miyaura; palladium; nickel; N-heterocyclic carbene; phosphine; polymerization Suzuki-Miyaura; palladium; nickel; N-heterocyclic carbene; phosphine; polymerization

Figure 1

This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

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Maluenda, I.; Navarro, O. Recent Developments in the Suzuki-Miyaura Reaction: 2010–2014. Molecules 2015, 20, 7528-7557.

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