Recent developments in copper-catalyzed reactions of diazo compounds

被引:320
|
作者
Zhao, Xia [1 ]
Zhang, Yan [2 ]
Wang, Jianbo [2 ]
机构
[1] Tianjin Normal Univ, Tianjin Key Lab Struct & Performance Funct Mol, Coll Chem, Tianjin 300387, Peoples R China
[2] Peking Univ, Coll Chem, Key Lab Bioorgan Chem & Mol Engn, Beijing Natl Lab Mol Sci,Minist Educ, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
H INSERTION REACTIONS; HIGHLY ENANTIOSELECTIVE INSERTION; ALPHA-DIAZOCARBONYL COMPOUNDS; MEDIATED DIRECT ARYLATION; ORGANIC-SYNTHESIS; CYCLOPROPANATION REACTIONS; 3-COMPONENT REACTION; CARBENOID INSERTION; TERMINAL ALKYNES; SULFUR YLIDES;
D O I
10.1039/c2cc34406h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Copper-catalyzed reaction of diazo compounds generates copper carbene intermediates that undergo diverse transformations. In recent years, the selectivity and efficiency of these important conversions have been further improved. In particular, breakthroughs have been made in catalytic asymmetric polar X-H bond insertion reactions. Moreover, novel transformations based on copper carbene, namely copper-catalyzed cross-couplings of diazo compounds, have emerged as powerful methods for carbon-carbon bond formations. This feature article summarizes the most recent developments in this area.
引用
收藏
页码:10162 / 10173
页数:12
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