Dirhodium-catalyzed one-step cascade intermolecular 1,4-diamination via cyclopropanation

被引:1
|
作者
Yang, Qi [1 ]
Liu, Xinyu [2 ]
Qin, Song [1 ]
Wang, Yuanhua [1 ]
机构
[1] Sichuan Univ, Coll Chem, Chengdu 610041, Peoples R China
[2] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2024年 / 11卷 / 17期
基金
美国国家科学基金会;
关键词
C-H AMINATION; N BOND-FORMATION; DIAMINATION; FUNCTIONALIZATION; THERMOCHEMISTRY; 1,3-DIAMINES; ACTIVATION; AMIDATION; ALKENES; IMINES;
D O I
10.1039/d4qo00826j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This work presents a novel dirhodium-catalyzed method for the conversion of aromatic hydrocarbons to 1,4-diamines using N-fluorobenzenesulfonimide (NFSI) as the nitrogen source. It is characterized by the activation of inert secondary and primary C(sp(3))-H bonds under mild conditions to yield 1,4-diaminated products. The methodology involves arylcyclopropane intermediates, as suggested by density functional theory (DFT) calculations. This approach not only simplifies the multifunctionalization of carbon frameworks, but also demonstrates the efficacy of the dirhodouim catalyst. It opens up new possibilities for C(sp(3))-H to C(sp(3))-N bond transformations, laying the groundwork for future developments in complex molecule synthesis.
引用
收藏
页码:4769 / 4778
页数:10
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