Suzuki-Miyaura cross-coupling reactions in aqueous media: Green and sustainable syntheses of biaryls
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AbstractCarbon-carbon cross-coupling reactions are among the most important processes in organic chemistry, and Suzuki-Miyaura reactions are among the most widely used protocols for the formation of carbon-carbon bonds. These reactions are generally catalyzed by soluble palladium complexes with various ligands. However, the use of toxic organic solvents remains a scientific challenge and an aspect of economical and ecological relevance. This Review will summarize various recently developed significant methods by which the Suzuki-Miyaura coupling was conducted in aqueous media, and analyzes if they are "real green" protocols. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
CitationPolshettiwar, V., Decottignies, A., Len, C., & Fihri, A. (2010). Suzuki-Miyaura Cross-Coupling Reactions in Aqueous Media: Green and Sustainable Syntheses of Biaryls. ChemSusChem, 3(5), 502–522. doi:10.1002/cssc.200900221
SponsorsWe thank G. Santini for his support of this work and the Region Picardie for their financial support.
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