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Elsevier, Journal of Organometallic Chemistry, 15-16(696), p. 2845-2849, 2011

DOI: 10.1016/j.jorganchem.2011.04.013

Wiley-VCH Verlag, ChemInform, 48(42), p. no-no, 2011

DOI: 10.1002/chin.201148068

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Microwave promoted Suzuki reactions between aroyl chlorides and boronic acids catalyzed by heterogeneous and homogeneous phosphine-free palladium catalysts

Journal article published in 2011 by Daniela de Luna Martins ORCID, Lúcia C. S. Aguiar, Octavio A. C. Antunes
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Suzuki cross-coupling reactions between arylboronic acids and aroyl chlorides with phosphine-free palladium catalysis under microwave irradiation were performed to obtainment of aromatic ketones in good yields within short times. Heterogeneous and homogeneous catalysts were studied as well as their influence in the reaction selectivity relative to homocoupling of the boronic acids.