催化作用
化学
废止
组合化学
芳基
药物化学
立体化学
有机化学
烷基
作者
Xiao-Na Wang,Yanan Wang,Nanfang Wang,Jinyue Chen,Chao Qi,Junbiao Chang
标识
DOI:10.1021/acs.joc.3c02342
摘要
Here, we disclose an efficient TMSOTf-catalyzed C–H annulation of aryl-terminated N-arylynamides with sulfilimines, leading to the practical assembly of various valuable 2-aminoindoles in generally moderate to excellent yields with a broad range of functional groups, while nonaryl terminated N-arylynamides undergo TMSOTf-catalyzed aminative arylation with sulfilimines providing α-arylated amidines.
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