A comprehensive account of recent advances in the synthesis of imidazopyridines, assisted
through transition-metal-catalyzed multicomponent reactions, C–H activation …

The discovery and optimization of a reaction between 2-chloropyridines and 2 H-azirines
producing imidazo [1, 2-a] pyridines is described. The treatment of 2 H-azirines with triflic …

The Selectfluor-mediated approach toward the synthesis of methylene-tethered
arylsulfonation and benzotriazolation of imidazopyridines has been described. The reaction …

An efficient route for the difluorinative-hydroxylation through dearomative difunctionalization
of imidazopyridine using Selectfluor as fluorine source has been developed in an aqueous …

We report herein, for the first time, the direct C–H bond arylation of imidazo [1, 2-a] pyridine
with aryl halides using monodisperse Ni@ Pd core@ shell nanoparticles assembled on …

An aerobic coupling of 2-aminopyrimidines or 2-aminopyridines with trans-chalcones to
afford aroylimidazo [1, 2-a] pyrimidines and aroylimidazo [1, 2-a] pyridines is reported …

A simple and an efficient method for the regioselective synthesis of N-alkyl/aryl/H 3-
arylindole derivatives from N-substituted anilines and trans-β-nitrostyrenes has been …

Conclusion In conclusion, we have developed a simple, mild, ecofriendly and relatively
inexpensive method for palladium-catalysed direct arylation of imidazo [1, 2-a] pyridines with …

The aim of present investigation is survey reactivity of 2-aminopyridine and Meldrum's acid
in the presence of aryl glyoxals or aryl aldehydes. The ethyl 2-(3-aryl imidazo [1, 2-a] pyridin …

Novel inhibitors are needed to tackle tuberculosis. Herein, we report the 3‐aryl‐substituted
imidazo [1, 2‐a] pyridines as potent antituberculosis agents. A small library of 3‐aryl …