2-Arylquinolines constitute a special class of compounds due to their importance in medicinal chemistry and functional materials.
A Heck–Matsuda cross-coupling reaction of a phenylalanine-derived arenediazonium salt with various alkenes has been used for the preparation of fluorescent unnatural α-amino acids.
Arenediazonium salts have gained attention in the scientific community due to numerous synthetic applications. Functionalization of arenediazonium salt using electricity offers sustainable, economic, and environmentally friendly chemical transformations for arylation, halogenation and annulation.
This paper demonstrates the electrochemical palladium-catalyzed selective C–H arylation of arenes using diazonium salts as a cost-effective aryl source, eliminating the need for chemical oxidants.
Synthesis of biaryls, terphenyls and cinnamates using a reduced graphene oxide-supported palladium nanoparticle (Pd@rGO)-based nanocatalyst with low palladium loadings.