Approaches to the Syntheses of Partially Reduced Imidazo[1,2-a]pyridines

被引:0
|
作者
Shin, Junhwa [1 ]
Nho, Young Chang [1 ]
Howard, Arthur S. [2 ]
机构
[1] Korea Atom Energy Res Inst, Adv Radiat Technol Inst, Jeongeup 580185, Jeonbuk, South Korea
[2] Eastern Michigan Univ, Dept Chem, Ypsilanti, MI 48179 USA
关键词
Aza-alkaloid; Heterocyclic compounds; Indolizidine;
D O I
10.5012/bkcs.2008.29.10.1998
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two synthetic pathways to substituted hexahydroimidazo[1,2-a]pyridines, which may serve as precursors of aza-alkaloids, were investigated. The first involves the condensation of a bisnucleophilic enediaminoester and a biselectrophile. The second involves attachment to nitrogen of the carbon chain skeleton required to form the six-memberd ring, before formation of the enediaminoester. Several substituted hexahydroimidazo[1,2-a]pyridines were synthesized via these two approaches.
引用
收藏
页码:1998 / 2004
页数:7
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