Silver-catalysed reactions of alkynes: recent advances

被引:495
作者
Fang, Guichun [1 ]
Bi, Xihe [1 ,2 ]
机构
[1] NE Normal Univ, Dept Chem, Changchun 130024, Peoples R China
[2] Nankai Univ, State Key Lab Elemento Organ Chem, Tianjin 300071, Peoples R China
关键词
ONE-POT SYNTHESIS; SILVER(I)-CATALYZED TANDEM REACTION; SILVER(I)-RHODIUM(I) COOPERATIVE CATALYSIS; HIGHLY REGIOSELECTIVE SYNTHESIS; CARBON-DIOXIDE INCORPORATION; ELECTRON-DEFICIENT ALKYNES; VERSATILE BUILDING-BLOCK; C-H FUNCTIONALIZATION; DIELS-ALDER REACTION; CONIA-ENE REACTION;
D O I
10.1039/c5cs00027k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Silver is a less expensive noble metal. Superior alkynophilicity due to p-coordination with the carbon-carbon triple bond makes silver salts ideal catalysts for alkyne-based organic reactions. This review highlights the progress in alkyne chemistry via silver catalysis primarily over the past five years (ca. 2010-2014). The discussion is developed in terms of the bond type formed with the acetylenic carbon (i.e., C-C, C-N, C-O, C-Halo, C-P and C-B). Compared with other coinage metals such as Au and Cu, silver catalysis is frequently observed to be unique. This critical review clearly indicates that silver catalysis provides a significant impetus to the rapid evolution of alkyne-based organic reactions, such as alkynylation, hydrofunctionalization, cycloaddition, cycloisomerization, and cascade reactions.
引用
收藏
页码:8124 / 8173
页数:50
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