Citation: Yue Guizhou, Liu Bo. Research Progress on [3+n] (n≥3) Cycloaddition of 1, 3-Diploes[J]. Chinese Journal of Organic Chemistry, ;2020, 40(10): 3132-3153. doi: 10.6023/cjoc202005092 shu

Research Progress on [3+n] (n≥3) Cycloaddition of 1, 3-Diploes

Yue Guizhou ^a,, ,
Liu Bo ^b,,

a.
School of Science, Sichuan Agricultural University, Ya'an, Sichuan 625014
b.
Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064

Corresponding author: Yue Guizhou, yueguizhou@sicau.edu.cn Liu Bo, chembliu@scu.edu.cn
Received Date: 30 May 2020
Revised Date: 19 June 2020
Available Online: 30 June 2020
Fund Project: Project supported by the Science and Technology Program of Sichuan Province (No. 2020YFH0129)Science and Technology Program of Sichuan Province 2020YFH0129

Figures(1)

Versatile heterocyclic skeletons extensively exist in structures of natural products, drug molecules and organic materials, and have been synthesized through various strategies reported in literatures. Among them, the 1, 3-dipolar cycloaddition is the most impressive class to build the related heterocycles. In the past, organic chemists generally employed[3+2] cycloaddition of 1, 3-dipoles to assemble five-membered rings. As modern chemistry developes, researchers further turn their attention to the[3+3], [3+4], [3+5] and[3+6] cycloadditions, to construct six-, seven-, eight- and bridge-heterocyclic compounds. At present, review articles with topics on 1, 3-dipolar cycloaddition mainly focus on[3+2] cycloaddition. Herein, A topic on[3+n] (n ≥ 3) cycloaddition of 1, 3-dipoles, with comments on the developed methodologies is present and the outlook in this field is proposed.
- 1, 3-diploar cycloaddtion,
- nitrone,
- azomethine ylide,
- azomethine imine,
- nitrile imine,
- nitrile oxide,
- nitrile ylide
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