119448-81-6Relevant articles and documents
Reactivity of 3-iodoimidazo[1,2-a]pyridines using a Suzuki-type cross-coupling reaction
Enguehard, Cecile,Renou, Jean-Louis,Collot, Valerie,Hervet, Maud,Rault, Sylvain,Gueiffier, Alain
, p. 6572 - 6575 (2000)
The influence of base and solvent in Suzuki cross-coupling reaction on various 2-substituted-3-iodoimidazo[1,2-a]pyridines was reported. The reactivity was largely influenced by nature of the substituent. Optimized yields and shortened times of reaction were obtained using strong bases in DME.
A mild and novel synthesis of functionalized fused imidazole analogues under environmentally benign reaction media
Babu, B. Madhu,Kumar, G. Santosh,Thakur, Pramod B.,Bangade, Vikas M.,Meshram
supporting information, p. 3473 - 3477 (2014/06/10)
A mild and novel approach is described for the synthesis of functionalized fused imidazole analogues in solvent-free and catalyst-free condition in ionic liquid. The short reaction time, good isolated yields, generality and environmentally benign reaction media are the significant features of this protocol.
Catalytic C-H arylation of SEM-protected azoles with palladium complexes of NHCs and phosphines
Toure, B. Barry,Lane, Benjamin S.,Sames, Dalibor
, p. 1979 - 1982 (2007/10/03)
The synthesis and catalytic evaluation of palladium complexes containing imidazolyl carbene ligand of varying steric and electronic properties is reported. These complexes catalyze the efficient C-H arylation of SEM-protected azole heteroarenes and thus provide a good method for preparation of a wide range of arylated free (NH)-azoles including pyrroles, indoles, imidazoles, and imidazo[1,2-a]pyridines. The reaction is operationally simple; the complexes are insensitive to moisture.