化学
吲哚试验
组合化学
催化作用
氧化还原
化学合成
有机化学
生物化学
体外
作者
Yun‐Tao Zheng,Jinshuai Song,Hai‐Chao Xu
标识
DOI:10.1021/acs.joc.1c00988
摘要
Indole is prevalent in bioactive compounds and natural products. The development of efficient and sustainable methods to access this privileged structural scaffold has been a long-standing interest of synthetic chemists. Herein, we report an electrocatalytic method for the synthesis of indoles through dehydrogenative cyclization of 2-vinylanilides. The reactions employ an organic redox catalyst and do not require any external chemical oxidant, providing speedy and efficient access to 3-substituted and 2,3-disubstituted indoles.
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