Preparation of Indolizine by Intramolecular 1,5-Dipolar Cycloaddition of Pyridinium N-Allylides

Chemical Research in Chinese Universities ›› 1998, Vol. 14 ›› Issue (2): 213-214.

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Preparation of Indolizine by Intramolecular 1,5-Dipolar Cycloaddition of Pyridinium N-Allylides

ZHOU Jian, HU Yue-fei, HU Hong-wen

Department of Chemistry, Nanjing University, Nanjing 210093

Received:1997-12-10 Online:1998-04-24 Published:2011-08-17
Supported by:
Supported by the National Natural Science Foundation of China.

Abstract

ZHOU Jian, HU Yue-fei, HU Hong-wen . Preparation of Indolizine by Intramolecular 1,5-Dipolar Cycloaddition of Pyridinium N-Allylides[J]. Chemical Research in Chinese Universities, 1998, 14(2): 213-214.

[1]	LIU Zhen-ming, WU Lei, SUN Jing, YAN Chao-guo. Efficient One-pot Synthesis of Pyrrolo[2,1-a]isoquinoline and Pyrrolo[1,2-a]quinoline Derivatives [J]. Chemical Research in Chinese Universities, 2012, 28(6): 990-993.
[2]	ZHU Chang-cheng, WEI Xu-dong, HU Jia-xin, WANG De-fen, HU Hong-wen. A Facile Synthesis of Indolizines by 1,3-Dipolar Cycloaddition of Pyridinium and Related Heteroaromatic Ylides with Alkenes in the Presence of TPCD, Py₄Co(HCrO₄)₂ [J]. Chemical Research in Chinese Universities, 1994, 10(2): 93-101.

Preparation of Indolizine by Intramolecular 1,5-Dipolar Cycloaddition of Pyridinium N-Allylides

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