Abstract
Aryl chlorides are noticeably uncommon partners in coupling reactions with heteroaromatics through C-H activation. We report herein that as little as 1 mol-% of the air-stable PdCl(dppb)(C3H5) complex catalyses the direct coupling of electron-deficient aryl chlorides with 2-substituted thiazole derivatives. A range of functionalities on the aryl chloride such as acetyl, formyl, ester, nitro, nitrile or trifluoromethyl is tolerated. © Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
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Gottumukkala, A. L., & Doucet, H. (2007). Activated aryl chlorides: Useful partners for the coupling with 2-substituted thiazoles in the palladium-catalysed C-H activation/ functionalisation reaction. European Journal of Inorganic Chemistry, (23), 3629–3632. https://doi.org/10.1002/ejic.200700420
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