Imidazopyridine is one of the important fused bicyclic 5–6 heterocycles and it is recognized
as a “drug prejudice” scaffold due to its wide range of applications in medicinal chemistry …

Advances in the last decade for the synthesis of the imidazo [1, 2-a] pyridine scaffold from
various substrates employing approaches such as multicomponent reactions, tandem …

A visible light mediated, metal-free process for the thiocyanation of imidazoheterocycles has
been developed using eosin Y as a photoredox catalyst under ambient air at room …

Development of an efficient, mild, economically viable, and green method for the
construction of a Csp2–Csp3 bond via coupling between a saturated hydrocarbon [(Csp3) …

Heterocycles have been found to be of much importance as several nitrogen-and oxygen-
containing heterocycle compounds exist amongst the various USFDA-approved drugs …

A direct and straightforward approach for highly regioselective thiocyanation of
imidazoheterocycles through sp2 C–H functionalization has been realized at room …

Iodine-catalyzed regioselective sulfenylation of imidazo [1, 2-a] pyridines via C (sp2)–H
bond functionalization has been achieved using sulfonyl hydrazides as a thiol surrogate. A …

A novel, efficient and practical method for copper-catalysed oxidative C-3 amination of
quinoxalin-2 (1H)-ones with primary or secondary amines as the nitrogen sources has been …

Nitrogen‐containing heterocycles have found remarkable applications in natural product
research, material sciences, and pharmaceuticals. Although the synthesis of this interesting …

Catalytic oxidative trifluoromethylation of imidazopyridines has been carried out at room
temperature through the functionalization of the sp2 C–H bond employing Langlois reagent …