Copper-catalyzed aromatic C-H bond cyanation by C-CN bond cleavage of inert acetonitrile

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Abstract

Cut and paste! A Cu-catalyzed aromatic C-H cyanation with acetonitrile as the nitrile source by C-CN cleavage has been developed (see scheme; TMEDA=N,N,N′,N′-tetramethylethylenediamine). The reaction is catalytic in copper, and it is found that using (Me3Si)2 as an additive plays a critical role in promoting C-CN cleavage and enhancing the reaction rate. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Kou, X., Zhao, M., Qiao, X., Zhu, Y., Tong, X., & Shen, Z. (2013). Copper-catalyzed aromatic C-H bond cyanation by C-CN bond cleavage of inert acetonitrile. Chemistry - A European Journal, 19(50), 16880–16886. https://doi.org/10.1002/chem.201303637

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