The term “C–H functionalisation” incorporates C–H activation followed by its transformation.
In a single line, this can be defined as the conversion of carbon–hydrogen bonds into …

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 …

Herein, an environmentally friendly electrochemical approach is reported that takes
advantage of the captodative effect and delocalization effect to generate nitrogen‐centered …

Water can accelerate a variety of organic reactions far beyond the rates observed in
classical organic solvents. However, using pure water as a solvent introduces solubility …

The intrinsic relationship between helicenes and circulenes is of fundamental interest and
importance in molecular engineering. Herein, electrophilic borylation of phenanthroline …

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 …

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 …

The preparation of N-containing heterocycles is always the core of synthetic chemistry.
Recently, oxidative coupling between two R–H nucleophiles is gaining more attention due to …

Hypervalent iodine chemistry is a rapidly growing area of research with tremendous impact
on synthetic chemistry in the past years. A rich and diverse chemistry is now available for …

A Cu (II)-catalyzed, inter/intramolecular C–N bond formation for the synthesis of various
benzimidazole-fused heterocycles in a concise manner has been reported. The robustness …