Development of Domino Reactions with β-Enamino Esters as Key Intermediates

doi:10.6023/cjoc201206008

Chin. J. Org. Chem. ›› 2012, Vol. 32 ›› Issue (9): 1577-1586.DOI: 10.6023/cjoc201206008 Previous Articles Next Articles

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β-烯胺酯为关键中间体的串联反应研究进展

韩莹, 孙晶, 孙岩, 高红, 颜朝国

扬州大学化学化工学院扬州 225002

收稿日期:2012-06-08 修回日期:2012-07-17 发布日期:2012-07-12
通讯作者: 颜朝国 E-mail:cgyan@yzu.edu.cn
基金资助:
国家自然科学基金(Nos.20972132, 21172189)资助项目

Development of Domino Reactions with β-Enamino Esters as Key Intermediates

Han Ying, Sun Jing, Sun Yan, Gao Hong, Yan Chaoguo

College of Chemistry & Chemical Engineering, Yangzhou University, Yangzhou 225002

Received:2012-06-08 Revised:2012-07-17 Published:2012-07-12
Supported by:
Project supported by the National Natural Science Foundation of China (Nos.20972132, 21172189)

Domino reactions have attracted much high attention in recent years due to its convergence, productivity, facile execution and generation of highly diverse and complex products from easily available starting materials in a single operation. Addition of primary amines to electron-deficient alkynes could generated reactive enaminone (ester) in mild conditions, which have shown versatile reactivity and have been widely used in domino procedure as key reactive intermediate to develop a number of carbon-carbon bond formation reactions, heterocyclic and spiro cyclic constructions. In this paper the recent developments of the domino reactions with enamino esters as key intermediates based on our experimental investigation are reviewed.

Key words: domino reaction, multicomponent reaction, electron-deficient alkyne, enamino ester, heterocycles, spirocycles

Cite this article

Han Ying, Sun Jing, Sun Yan, Gao Hong, Yan Chaoguo. Development of Domino Reactions with β-Enamino Esters as Key Intermediates[J]. Chin. J. Org. Chem., 2012, 32(9): 1577-1586.

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β-烯胺酯为关键中间体的串联反应研究进展

Development of Domino Reactions with β-Enamino Esters as Key Intermediates

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