4.5 Article

Recent Advances in the Palladium Catalyzed Suzuki-Miyaura Cross-Coupling Reaction in Water

Journal

CATALYSIS LETTERS
Volume 146, Issue 4, Pages 820-840

Publisher

SPRINGER
DOI: 10.1007/s10562-016-1707-8

Keywords

Cross-coupling; Palladium; Aqueous catalysis; Green chemistry; Sustainable chemistry

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The palladium-catalyzed Suzuki-Miyaura cross-coupling reaction of organic halides with boronic acids is one of the most versatile methods for the synthesis of biaryls. Green chemistry is a rapidly developing new field that provides us a proactive avenue for the sustainable development of future science and technologies. When designed properly, clean chemical technology can be developed in water as a reaction medium. The technologies generated from such green chemistry endeavours may often be cheaper and more profitable. This review covers the literature on palladium-catalysed the Suzuki-Miyaura cross-coupling reaction in water.

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