Recent advances in transition metal-catalyzed N-atom transfer reactions of azides

被引:352
|
作者
Driver, Tom G. [1 ]
机构
[1] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
基金
美国国家卫生研究院;
关键词
C-H AMINATION; RU(SALEN)-CATALYZED ASYMMETRIC SULFIMIDATION; IRON(II)-MEDIATED NITRENE TRANSFER; FLASH VACUUM PYROLYSES; RAY CRYSTAL-STRUCTURE; ONE-POT SYNTHESIS; ARYL AZIDES; AROMATIC SUBSTITUTION; SECONDARY-AMINES; CLICK CHEMISTRY;
D O I
10.1039/c005219c
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Transition metal-catalyzed N-atom transfer reactions of azides provide efficient ways to construct new carbon-nitrogen and sulfur-nitrogen bonds. These reactions are inherently green: no additive besides catalyst is needed to form the nitrenoid reactive intermediate, and the by-product of the reaction is environmentally benign N(2) gas. As such, azides can be useful precursors for transition metal-catalyzed N-atom transfer to sulfides, olefins and C-H bonds. These methods offer competitive selectivities and comparable substrate scope as alternative processes to generate metal nitrenoids.
引用
收藏
页码:3831 / 3846
页数:16
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