A mild palladium-catalyzed Suzuki coupling reaction of quinoline carboxylates with boronic acids

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Abstract

A palladium-catalyzed cross-coupling between aryl carboxylates and boronic acids has been achieved for the first time by taking advantage of the enhanced reactivity of quinoline 4-carboxylates. Also for the first time a Suzuki coupling reaction via a self-activation of boronic acids without addition of base is described. The reactions proceed under mild conditions (25-65°C) to give excellent yields, and a wide range of functionalities is tolerated. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Li, W., Gao, J. J., Zhang, Y., Tang, W., Lee, H., Fandrick, K. R., … Senanayake, C. H. (2011). A mild palladium-catalyzed Suzuki coupling reaction of quinoline carboxylates with boronic acids. Advanced Synthesis and Catalysis, 353(10), 1671–1675. https://doi.org/10.1002/adsc.201100141

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