Abstract
Suzuki-Miyaura Cross-Coupling allows one to make a new C-C bond between an organic halide and a boronic acid, in the presence of a base and a metal catalyst, which Palladium is the most used one. In this work, we study the mechanism of a Suzuki-Miyaura coupling with Arildiazonium Salts, in the absence of a base, using Nickel as a catalyst, and glycerol as a solvent. We hope that the catal…