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The Suzuki-Miyaura reaction performed using a palladium-N-Heterocyclic carbene catalyst and a weak inorganic base

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Nolan_2015_EJOC_Suzuki_AM.pdf (516.0Kb)
Date
2015
Author
Izquierdo, Frederic
Corpet, Martin Michel Alfred Eton
Nolan, Steven Patrick
Keywords
Catalysis
Cross-coupling
NHC
Palladium
Suzuki-Miyaura
QD Chemistry
NDAS
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Abstract
N-Heterocyclic carbenes (NHCs) have been shown to be useful ligands for the Suzuki-Miyaura cross-coupling at low catalyst loadings. We now report that the commercially available and air-stable [Pd(IPr)(cin)Cl] pre-catalyst permits the formation of various functionalized biaryls from aryl chlorides and boronic acids (37 examples) under very mild conditions using a mixture of ethanol/water as solvent and an inorganic base.
Citation
Izquierdo , F , Corpet , M M A E & Nolan , S P 2015 , ' The Suzuki-Miyaura reaction performed using a palladium-N-Heterocyclic carbene catalyst and a weak inorganic base ' , European Journal of Organic Chemistry , pp. 1920-1924 . https://doi.org/10.1002/ejoc.201500043
Publication
European Journal of Organic Chemistry
Status
Peer reviewed
DOI
https://doi.org/10.1002/ejoc.201500043
ISSN
1434-193X
Type
Journal article
Rights
Copyright © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the accepted version of the following article: Izquierdo, F., Corpet, M. and Nolan, S. P. (2015), The Suzuki–Miyaura Reaction Performed Using a Palladium–N-Heterocyclic Carb­ene Catalyst and a Weak Inorganic Base. Eur. J. Org. Chem., which has been published in final form at: http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201500043/abstract
Description
We gratefully acknowledge the EC for funding through the seventh framework program SYNFLOW, the ERC (Advanced Investigator Award ‘FUNCAT’ to SPN) and the EPSRC. S.P.N. is a Royal Society Wolfson Research Merit Award holder.
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  • University of St Andrews Research
URL
http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201500043/suppinfo
URI
http://hdl.handle.net/10023/8252

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