Aktas, AydinAkkoc, SenemGok, Yetkin2024-08-042024-08-0420130095-89721029-0389https://doi.org/10.1080/00958972.2013.819092https://hdl.handle.net/11616/96216Naphthalenomethyl-substituted imidazolidinium salts (1a-g) were prepared and characterized by conventional spectroscopic methods, H-1 NMR, C-13 NMR, FTIR, and elemental analysis techniques. The in situ prepared three component systems naphthalenomethyl-substituted imidazolidinium salts, Pd(OAc)(2), and K2CO3 catalyzed quantitatively the Mizoroki-Heck and Suzuki-Miyaura coupling of aryl halides under mild conditions in aqueous media.eninfo:eu-repo/semantics/closedAccessImidazolidinium saltMizoroki-Heck reactionSuzuki-Miyaura reactionCatalystN-Heterocyclic carbenePalladium catalyzed Mizoroki-Heck and Suzuki-Miyaura reactions using naphthalenomethyl-substituted imidazolidin-2-ylidene ligands in aqueous mediaArticle66162901290910.1080/00958972.2013.8190922-s2.0-84884535520Q3WOS:000324365600011Q2