异喹啉
化学
烯烃
钯
催化作用
苯
酚类
羰基化
有机化学
药物化学
一氧化碳
作者
Siqi Wang,Jian‐Shu Wang,Jun Ying,Xiao‐Feng Wu
标识
DOI:10.1016/j.cclet.2022.107873
摘要
A novel palladium-catalyzed carbonylative cyclization of alkene-tethered indoles with phenols or arylboronic acids is described, which provides a facile approach to access indolo[2,1-a]isoquinoline scaffolds. This method employs benzene-1,3,5-triyl triformate (TFBen) as the CO surrogate for the incorporation of a carbonyl group into indolo[2,1-a]isoquinoline scaffolds, and a variety of carbonyl-containing indolo[2,1-a]isoquinoline derivatives are prepared in good yields.
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