Recent Advances in Iron-Catalyzed C-H Bond Amination via Iron Imido Intermediate

被引:87
|
作者
Wang, Peng [1 ]
Deng, Liang [1 ]
机构
[1] Chinese Acad Sci, State Key Lab Organometall Chem, Ctr Excellence Mol Synth, Shanghai Inst Organ Chem,Univ Chinese Acad Sci, 345 Lingling Rd, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H bond activation; iron; imido; nitrene; hydrogen atom abstraction; HYDROGEN-ATOM TRANSFER; NITRENE TRANSFER-REACTIONS; SATURATED-HYDROCARBONS; C(SP(3))-H AMINATION; CARBENE INSERTION; NITRIDO COMPLEXES; TANDEM REACTIONS; NITROGEN-SOURCE; ARYL AZIDES; FUNCTIONALIZATION;
D O I
10.1002/cjoc.201800427
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal-catalyzed C-H bond amination reaction is an attractive method for the synthesis of amines. Fueled by the growing interests in the development of economical and eco-friendly catalysts for organic transformations, there are great recent efforts on developing iron-catalyzed C-H bond amination reactions using organic azides, sulfonyl azides, and iminoiodanes as nitrene source. This review summarizes the progress achieved in the field since 2011. The reaction scope, the synthetic utility of the catalytic reaction, and the current mechanistic understandings of the C-H bond amination reactions catalyzed by hemoproteins, iron porphyrins and phthalocyanines, non-heme-type iron complexes, as well as metal-organic- framework-supported iron complexes are introduced and discussed.
引用
收藏
页码:1222 / 1240
页数:19
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