C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with
notable applications to material sciences, crop protection, drug discovery, and …

Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles |
Chemical Reviews ACS ACS Publications C&EN CAS Find my institution Log In Chemical …

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

2′-Aminoacetophenones undergo a C (sp3)–H oxidation followed by intramolecular C–N
bond formation by virtue of a simple electrochemical oxidation in the presence of n-Bu4NI …

A mechanistic study of the copper-catalyzed oxidation of the methylene group of aryl (di)
azinylmethanes was performed. Initial reaction rates were measured making use of in situ IR …

A highly efficient molecular iodine mediated formal [3+ 2+ 1] cycloaddition reaction for the
direct synthesis of substituted quinolines from methyl ketones, arylamines, and styrenes is …

A regioselective green approach for the nickel (II)-catalyzed C–N cross-coupling between
arylamines and pyrazoles through a photoredox process is reported. Moderate to good yield …

A copper (II)-catalyzed tandem reaction between pyridine ketone and benzylamine was
developed by using clean O2 as an oxidant. This transformation proceeded via an efficient …

Synthesis of isatin and iodoisatin from 2′-aminoacetophenone was achieved via oxidative
amido cyclization of the sp3 C–H bond using I2–TBHP as the catalytic system. The reaction …

A transition metal (TM)-free practical synthesis of biologically relevant benzoxazinones has
been established via a selective oxidative decarbonylative cleavage of an unstrained C (sp …