Progress of Iridium-Catalyzed Cycloaddition Reactions

被引：0
|
作者：
Bian, Hongxu [1 ]
Yang, Dingqiao [1 ]
机构：
[1] S China Normal Univ, Sch Chem & Environm, Guangzhou 51006, Guangdong, Peoples R China
来源：
CHINESE JOURNAL OF ORGANIC CHEMISTRY | 2010年 / 30卷 / 04期
关键词：
iridium catalysis; cycloaddition; iridium complex; KHAND-TYPE REACTION; 1,3-DIPOLAR CYCLOADDITION; ENANTIOSELECTIVE SYNTHESIS; ACETYLENE CYCLIZATIONS; RHODIUM; IR; DIYNES; RH; CYCLOTRIMERIZATION; ALPHA; OMEGA-DIYNES;
D O I：
暂无
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Transition metal-catalyzed cycloaddition reaction of unsaturated substances, such as alkynes and alkenes, is one of the most important methods for the synthesis of mono-ring and multi-ring systems. In this paper, the recent progress in iridium-catalyzed cycloaddition reactions is reviewed, mainly including [2+2+1], [2+2+2], [4+2], 1,3-dipolar cycloaddition reactions. In addition, some iridium-catalyzed [3+2+2], [3+2] and [5+1] cycloaddition reactions are described. Some parts of cycloaddition reaction mechanisms are also discussed.
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页码：506 / 514
页数：9
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