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Tobisu, Mamoru,Nakamura, Ryo,Kita, Yusuke,Chatani, Naoto Korean Chemical Society 2010 Bulletin of the Korean Chemical Society Vol.31 No.3
A rhodium-catalyzed reductive cleavage reaction of carbon-cyano bonds is developed using hydrosilane as a mild reducing agent. A wide range of nitriles, including aryl, benzyl, and $\beta$-hydrogen containing alkyl cyanides are applicable to this decyanation reaction. The method is also applicable to organic synthesis, in which benzyl cyanide is used as a benzyl anion equivalent and a cyano group functions as a removable ortho-directing group.
Mamoru Tobisu,Ryo Nakamura,Yusuke Kita,Naoto Chatani 대한화학회 2010 Bulletin of the Korean Chemical Society Vol.31 No.3
A rhodium-catalyzed reductive cleavage reaction of carbon-cyano bonds is developed using hydrosilane as a mild reducing agent. A wide range of nitriles, including aryl, benzyl, and β-hydrogen containing alkyl cyanides are applicable to this decyanation reaction. The method is also applicable to organic synthesis, in which benzyl cyanide is used as a benzyl anion equivalent and a cyano group functions as a removable ortho-directing group.