Scope of the palladium-catalyzed aryl borylation utilizing bis-boronic acid

GA Molander, SLJ Trice, SM Kennedy…

文献索引：Molander, Gary A.; Trice, Sarah L. J.; Kennedy, Steven M.; Dreher, Spencer D.; Tudge, Matthew T. Journal of the American Chemical Society, 2012 , vol. 134, # 28 p. 11667 - 11673

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被引用次数: 62

摘要

The Suzuki-Miyaura reaction has become one of the more useful tools for synthetic organic chemists. Until recently, there did not exist a direct way to make the most important component in the coupling reaction, namely the boronic acid. Current methods to make boronic acids often employ harsh or wasteful reagents to prepare boronic acid derivatives and require additional steps to afford the desired boronic acid. The scope of the previously ...