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Electrochemically promoted oxidative α-cyanation of tertiary and secondary amines using cheap AIBN.

Qing-Wen GuiZhi-Yuan XiongFan TengTian-Cheng CaiQiang LiWenxia HuXiaoli WangJialing YuXiaoying Liu
Published in: Organic & biomolecular chemistry (2021)
The electrochemical α-cyanation of tertiary and secondary amines has been developed by using a cheap cyanide reagent, azobisisobutyronitrile (AIBN). The CN radical, generated through n-Bu4NBr-meidated electrochemical oxidation, participates in a novel α-cyanation reaction under exogenous oxidant-free conditions.
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