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Issue 44, 2016
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Palladacycle catalysis: an innovation to the Suzuki–Miyaura cross-coupling reaction

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Abstract

Herein we report a Suzuki–Miyaura type cross-coupling between an aryl halide and a functionalized boronic acid palladacycle in the absence of an external catalyst. This reaction is an unprecedented case of catalysis in palladium metallacycle chemistry.

Graphical abstract: Palladacycle catalysis: an innovation to the Suzuki–Miyaura cross-coupling reaction

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Publication details

The article was received on 11 Sep 2016, accepted on 18 Oct 2016 and first published on 18 Oct 2016


Article type: Communication
DOI: 10.1039/C6DT03542F
Citation: Dalton Trans., 2016,45, 17598-17601
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    Palladacycle catalysis: an innovation to the Suzuki–Miyaura cross-coupling reaction

    F. Lucio-Martínez, L. A. Adrio, P. Polo-Ces, J. M. Ortigueira, J. J. Fernández, H. Adams, M. T. Pereira and J. M. Vila, Dalton Trans., 2016, 45, 17598
    DOI: 10.1039/C6DT03542F

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