Convenient synthesis of alkenyl-, alkynyl-, and allenyl-substituted imidazo[1,2-a]pyridines via palladium-catalyzed cross-coupling reactions

被引:21
作者
Enguehard-Gueiffier, Cecile [1 ]
Croix, Cecile [1 ]
Hervet, Maud [1 ]
Kazock, Jean-Yves [1 ]
Gueiffier, Alain [1 ]
Abarbri, Mohammed [2 ]
机构
[1] Univ Tours, SPOT EA 3857, Fac Pharm, F-37200 Tours, France
[2] Univ Tours, SPOT EA 3857, Fac Sci, F-37200 Tours, France
基金
美国国家科学基金会;
关键词
D O I
10.1002/hlca.200790241
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A systematic study on the Stille and Sonogashira cross-coupling of iodinated imidazo[1,2-a]pyridines was performed, permitting the preparation of various vinyl-, ethynyl-, and allenyl-substituted derivatives. These methods are particularly valuable, given their experimental simplicity and high degree of flexibility with regard to functional groups that can be introduced in positions 3, 6, or 8 of the imidazo[1,2-a]pyridine core. Effects concerning different substitution positions and the nature of the 2-substituent under various reaction conditions are reported in detail for the above types of unsaturated groups introduced.
引用
收藏
页码:2349 / 2367
页数:19
相关论文
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