Transition metal-mediated formation of C–N bonds is an essential synthetic methodology.
The discovery of the Chan–Lam amination provided a C–N bond forming process that was …

N‐Heteroaryl sulfonamides are an extremely significant variety of organosulfur compounds
that are present in many significant FDA‐approved drugs and therapeutic agents. Therefore …

A Cu (II) fluoride-catalyzed N-arylation of 7-azaindole N-oxides (7-AINO) has been
developed using boronic acid under base-free conditions. During the process, a …

Direct N‐arylation of sulfonamides is a very attractive approach for preparing
pharmaceutically important N‐(hetero) aryl sulfonamides because it avoids the potential …

A heterogeneous photocatalyst based on copper modified phosphorus doped g-C3N4 (Cu/P-
CN) has been prepared and characterized. This recyclable catalyst exhibited high …

Due to their three-dimensional structure, chemical and metabolic stability, polarity, and
hydrogen-bonding ability, sulfonamides occupy a privileged position among the functional …

Simple copper salts serve as catalysts to effect C–X bond-forming reactions in some of the
most utilized transformations in synthesis, including the oxidative coupling of aryl boronic …

Copper (III) fluorides are catalytically competent, yet elusive, intermediates in cross‐
coupling. The synthesis of [PPh4][CuIII (CF3) 3F](2), the first stable (isolable) CuIII− F, was …

Developing catalytic reactions for organic synthesis is the central goal of countless research
groups worldwide. High-throughput experimentation is invaluable for this pursuit, with the …

N-Arylation of NH-sulfoximines represents an appealing approach to access N-aryl
sulfoximines, but has not been successfully applied to NH-diaryl sulfoximines. Herein, a …