电泳剂
化学
芳基
催化作用
废止
组合化学
有机化学
药物化学
立体化学
烷基
作者
Lixia Ding,Nanfang Wang,Chaofan Qi,Jinyue Chen,Junbiao Chang,Xiaona Wang
标识
DOI:10.1021/acs.joc.4c01712
摘要
The efficient synthesis of 1-amino-1H-indenes and 2,4-dienamides was realized via TfOH-catalyzed reactions of aryl methyl ketones with terminal ynamides in two distinct pathways. Aromatic ketones with high electrophilicity underwent [3 + 2] annulation with ynamides to produce 1-amino-1H-indenes, while aromatic ketones with low electrophilicity proceeded under the same conditions to afford 2,4-dienamides. Furthermore, the obtained 1-amino-1H-indenes could be converted into the corresponding 1H-indenes and dihydro-1H-indenes in excellent yields.
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