化学
废止
铑
阿托品
催化作用
对偶(语法数字)
氧化还原
双重角色
药物化学
立体化学
组合化学
有机化学
文学类
艺术
作者
Siyuan Li,Yong Han,Zhen Yang,Chen Wang,Ruokun Feng,Minfeng Zeng,Zhanxiang Liu,Yuhong Zhang
出处
期刊:Organic Letters
[American Chemical Society]
日期:2025-04-22
卷期号:27 (18): 4626-4631
标识
DOI:10.1021/acs.orglett.5c00676
摘要
A rhodium(III)-catalyzed dual-ring formation via cascade C-H activation/[4 + 2] annulation of 3,5-diaryoxadiazoles with alkynes was developed. This strategy has been demonstrated with a variety of 3,5-diaryloxadiazoles and alkynes, and it has been successfully scaled up to gram-scale synthesis, highlighting its potential significance in the direct construction of C-N atropisomers. Furthermore, the cleavage of the N-O bond is essential for the formation of the bicyclic structure in the absence of an external oxidant. Mechanistic studies revealed that cleavage of the C-H bond at the 3-phenyl group of oxadiazole was likely a rate-determining step in this reaction.
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