This Mini-Review highlights the most effective protocols for metal-free direct synthesis of
imidazo [1, 2-a] pyridines, crucial target products and key intermediates, developed in the …

Imidazo [1, 2-a] pyridine has gained much interest in the field of drug development because
of its strong medicinal properties, therefore the discovery of novel methods for its synthesis …

This review focuses on providing comprehensive highlights of the recent synthetic pathways
of imidazo [1, 2‐a] pyridines, assisted through transition metal‐catalyzed reactions, multi …

Herein, we report a metal-free one-pot three-component reaction of aryl methyl ketones, 2-
aminopyridines, and barbituric acids for the synthesis of pyrimidine-linked imidazopyridines …

I2/TBHP-promoted, one-pot, multi pathway synthesis of imidazopyridines and thiazoles has
been achieved through readily available ethylarenes, ethylenearenes and ethynearenes …

Heterocycles and their derivatives have been inspiring medicinal chemists to device novel,
greener and efficient ways to synthesized them as the majority of drugs available in the …

Imidazopyridines constitute one of the most important scaffolds in medicinal chemistry, as
their skeleton could be found in a myriad of biologically active molecules. Although …

Deconstruction of alkenes to their carbonyl derivatives is a widely used protocol in synthetic
organic chemistry and several reaction conditions have been demonstrated for electron-rich …

An efficient method for transition metal-free halogen bond-assisted regioselective C–H
arylation of 2-phenylimidazo-[1, 2-a] pyridines under visible-light condition has been …

Our study proposes an approach to semiheterogeneous photocatalysis, focusing on
recyclability challenges. We developed a method employing visible light with photoinert …