New amination strategies based on nitrogen-centered radical chemistry

被引:544
作者
Xiong, Tao [1 ]
Zhang, Qian [1 ]
机构
[1] NE Normal Univ, Dept Chem, Changchun 130024, Peoples R China
关键词
C-H AMINATION; AMIDATION; IMIDATION; ALDEHYDES; AZIDES; ARENES; FUNCTIONALIZATION; AMINOFLUORINATION; HYDROAMINATION; DIAMINATION;
D O I
10.1039/c5cs00852b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interesting and diverse biological activities of nitrogen-containing compounds make the construction of the C-N bond of great importance. Despite the tremendous advances that have been made in this research field, C-N bond formation based on nitrogen-centered radicals remains a significant challenge due to the harsh conditions required for the generation of nitrogen-centered radicals and their propensity for hydrogen abstraction or engaging in other degradation pathways. In the past several years, novel methodologies for C-N bond constructions based on nitrogen centered-radical intermediates, coordinated with metal or generated in the presence of visible-light and a photocatalyst, have attracted considerable attention. This tutorial review will summarize the significant progress of these efficient and mild radical amination reactions, with an emphasis on approaches for the generation of nitrogen-centered radicals and their reaction patterns, related mechanisms and synthetic applications, as well as unmet challenges in this emerging and promising field.
引用
收藏
页码:3069 / 3087
页数:19
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