Copper-Catalyzed sp3 C-H Amination

被引:292
作者
Gephart, Raymond T., III [1 ]
Warren, Timothy H. [1 ]
机构
[1] Georgetown Univ, Dept Chem, Washington, DC 20057 USA
基金
美国国家科学基金会;
关键词
AEROBIC OXIDATIVE AMINATION; N BOND FORMATION; ALLYLIC AMINATION; ALKENE AZIRIDINATION; NITRENE TRANSFER; ARYL AZIDES; INTERMOLECULAR AMINATION; MECHANISTIC ASPECTS; EFFICIENT SYNTHESIS; CUPROUS CHLORIDE;
D O I
10.1021/om300840z
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Among the transition metals, copper based catalyst systems enable the widest range of N-containing reagents in C-H amination to allow for the direct incorporation of versatile N-based functionalities via ubiquitous C H bonds. In addition to nitrene-based approaches involving sulfonyliminoiodinanes: (PhI=NSO2R), diverse non-nitrene protocols have been developed that allow for the direct use of organic amides, nitrosoarenes, and hydroxylamines, strained heterocycles such as oxaziridines, acetonitrile, secondary sulfonylamines, and even alkylamines and arylamines. Synthetic, Mechanistic, and theoretical studies reveal discrete copper nitrenes [Cu]=NR and copper amides [Cu]-NHR to be key reactive intermediates in C-H amination. Copper catalyzed sp(3) C-H amination is reviewed connecting catalytic reactivity patterns with likely copper intermediates wherever possible, with the goal to stimulate the further development Of C H functionalization reactions With copper which possess significant sustainability advantages over other Contemporary approaches involving noble metals.
引用
收藏
页码:7728 / 7752
页数:25
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