Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles |
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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 …

Particular success has been achieved in the synthesis of new products and in processes
since the twelve principles of “green chemistry” were formulated in the 1990s. These …

Electrochemical synthesis offers a mild, simple, and efficient tool for the preparation of
interesting and useful molecules, thus eluding severe chemical oxidizing and reducing …

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 …

N-Chlorosuccinimide-Promoted Regioselective Sulfenylation of Imidazoheterocycles at Room
Temperature | Organic Letters Recently Viewedclose modal ACS ACS Publications C&EN CAS …

Abstract Imidazo [1, 2-a] pyridines are unique nitrogen-containing organic compounds with
wide applications in pharmaceuticals, natural products, material science and …

The imidazo [1, 2-a] pyridine scaffold is recognized as a privileged structure as it represents
a promising area for identification of lead structures towards the discovery of new synthetic …

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 …