化学
分子内力
废止
过渡金属
甲亚胺叶立德
催化作用
亲核细胞
双环分子
金属
药物化学
立体化学
光化学
有机化学
环加成
1,3-偶极环加成
作者
Jie Ren,Chao Pi,Xiuling Cui,Yangjie Wu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2023-04-10
卷期号:25 (15): 2582-2587
被引量:15
标识
DOI:10.1021/acs.orglett.3c00472
摘要
Transition metal-controlled divergent annulation reactions of azomethine imines with iodonium ylides via C-centered [1,2]-rearrangement have been developed. The azomethine imino group, as a switchable and transient directing group (DG), underwent intramolecular nucleophilic addition and in situ generated bicyclic diaziridine, which facilitated the C-centered [1,2]-rearrangement and subsequent divergent annulations in the presence of different metal complexes as the catalysts. The benzo[c]chromen-1-one and pyrano[de]isochromene scaffolds could be independently constructed with Rh(III) and Ru(II), respectively. It was worth noting that the azomethine imino group was employed first as the switchable DG through rearrangement progress.
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