分子内力
化学
钯
甲烷氧化偶联
氧化磷酸化
催化作用
级联
组合化学
立体化学
有机化学
色谱法
生物化学
作者
Yu Dong,Mei-Feng Lan,Yue-Qin Lin,Lin Chen,Chunmei Wu,Zhifan Wang,Zhichuan Shi,Guowei Deng,Bing He
标识
DOI:10.1021/acs.joc.4c00545
摘要
We report a step-economic strategy for the direct synthesis of spiro polycyclic N-heterocycles and indolecarbazole-fused naphthoquinones by merging oxidative coupling and cascade palladium-catalyzed intramolecular oxidative cyclization. In the protocol, bi-indolylnaphthoquinones were first synthesized by oxidative coupling of indoles and naphthoquinones. Subsequent cascade palladium-catalyzed intramolecular oxidative cyclization of bi-indolylnaphthoquinones gave spiro polycyclic N-heterocycles and indolecarbazoles. The intramolecular oxidative cyclization approach could also be realized by the presence or absence of iron catalysts under standard conditions. This protocol is featured with moderate to excellent yields, a wide substrate scope, and divergent structures of products.
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