Özdemir, IGürbüz, NGök, YÇetinkaya, EÇetinkaya, B2024-08-042024-08-0420050936-5214https://doi.org/10.1055/s-2005-872673https://hdl.handle.net/11616/94110A highly effective, easy to handle, and environmentally benign process for palladium-mediated Suzuki cross-coupling was developed. The in situ prepared three-component system of Pd(OAc)(2), 1,3-dialkyltetrahydrodiazepinium chlorides (2a-e), and K2CO3 catalyzes quantitatively the Suzuki-Miyaura cross-coupling of deactivated aryl chloride.eninfo:eu-repo/semantics/closedAccesstetrahydrodiazepiniumSuzuki-Miyaura reactionpalladiumC-C couplingN-heterocyclic carbenePalladium-catalyzed Suzuki-Miyaura reaction of aryl chlorides in aqueous media using tetrahydrodiazepinium salts as carbene ligandsArticle152394239610.1055/s-2005-8726732-s2.0-25444478352Q2WOS:000232045500034Q1