118001-59-5Relevant articles and documents
One-Pot Synthesis of 3-Methyl-2-arylimidazo[1,2-a]pyridines Using Calcium Carbide as an Alkyne Source
Chen, Wei,Li, Zheng
, p. 76 - 84 (2022/01/03)
An efficient method for the construction of 3-methyl-2-arylimidazo[1,2-a]pyridines from the reactions of calcium carbide, 2-aminopyridines, and aromatic aldehydes is described. The notable advantages for this strategy include the use of an inexpensive and
Iron(III)-catalyzed denitration reaction: One-pot three-component synthesis of imidazo[1,2-a]pyridine derivatives
Yan, Hao,Wang, Yuling,Pan, Congming,Zhang, Hao,Yang, Sizhuo,Ren, Xiaoyu,Li, Jian,Huang, Guosheng
, p. 2754 - 2763 (2014/05/06)
An iron(III)-catalyzed one-pot three-component cross-coupling nitration reaction of 2-aminopyridines, aldehydes and nitroalkanes, straightforwardly forms imidazo[1,2-a]pyridine derivatives and is described in this report. The system shows good functional-group tolerance and proceeds smoothly in moderate to good yields. An iron(III)-catalyzed one-pot three-component cross-coupling nitration reaction of 2-aminopyridines, aldehydes, and nitroalkane, leading to the straightforward formation of imidazo[1,2-a]pyridine derivatives has been reported. In this procedure, the starting materials are commercially available. The system shows good functional-group tolerance and proceeds smoothly in moderate to good yields. Copyright
Iron(II)-catalyzed denitration reaction: Synthesis of 3-methyl-2- arylimidazo[1,2-a]pyridine derivatives from aminopyridines and 2-methylnitroolefins
Yan, Hao,Yang, Sizhuo,Gao, Xiai,Zhou, Kang,Ma, Chao,Yan, Rulong,Huang, Guosheng
supporting information, p. 2961 - 2964 (2013/02/22)
A variety of ways to synthesize imidazo[1,2-a]pyridines have been reported and many approaches are devoted to the functionalization of imidazo[1,2-a] pyridines. However, the use of a denitration reaction in the synthesis of imidazo[1,2-a]pyridines has not
