化学
钯
废止
金属化
区域选择性
催化作用
三氟甲磺酸
芳基
镍
脱质子化
苯并环丁烯
组合化学
药物化学
有机化学
离子
烷基
聚合物
作者
Jingfeng Huo,Yue Fu,Melody J. Tang,Peng Liu,Guangbin Dong
摘要
While Catellani reactions have become increasingly important for arene functionalizations, they have been solely catalyzed by palladium. Here we report the first nickel-catalyzed Catellani-type annulation of aryl triflates and chlorides to form various benzocyclobutene-fused norbornanes in high efficiency. Mechanistic studies reveal a surprising outer-sphere concerted metalation/deprotonation pathway during the formation of the nickelacycle, as well as the essential roles of the base and the triflate anion. The reaction shows a broad functional group tolerance and enhanced regioselectivity compared to the corresponding palladium catalysis.
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