N-arylation reaction has become one of the key strategies in organic synthesis to access
several molecules of biological, agrochemical, and medicinal importance. The century-old …

A polyimide covalent organic framework (PI-COF) with high thermal and chemical stabilities
has been readily prepared from commercially available and inexpensive reagents and was …

Copper (II) pyridyliminoarylsulfonate complexes with chloride or triflate counteranions were
employed in Chan–Evans–Lam (CEL) couplings of N-nucleophiles and arylboronic acids …

Copper-mediated carbon–heteroatom bond-forming reactions involving a wide range of
substrates have been in the spotlight for many organic chemists. This review highlights …

The aminopyridines are key building blocks in the synthesis of bioactive heterocyclic
compounds such as azaindoles and imidazopyridines. The role of metal‐catalyzed methods …

A new strategy is developed for the synthesis of 1-aminoisoquinoline derivatives. This Rh
(III)-catalyzed [4+ 2] annulation reaction employs benzamidines as efficient directing groups …

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 …

The synthesis of a novel mesoporous covalent imine polymeric (MCIPs) material, involving
simple Schiff‐base chemistry, is reported. This highly functionalised nitrogen‐rich material …

Copper (II)-catalyzed boronic acid promoted chemoselective N-arylation of unprotected
aminophenols has been developed. Selective N-arylation of 3-aminophenol is achieved …

Copper (II)-catalyzed boronic acid promoted C–N bond cross-coupling reactions have been
successfully developed for sequential N-arylation of C-amino-NH-azoles. These general …