Palladium-catalysed Suzuki reaction of aryl chlorides in aqueous media using 1,3-dialkylimidazolidin-2-ylidene ligands

Özdemir, IDemir, SYasar, SÇetinkaya, B2024-08-042024-08-0420050268-26051099-0739https://doi.org/10.1002/aoc.793https://hdl.handle.net/11616/93799A highly effective, easy to handle and environmentally benign process for palladium-mediated Suzuki cross-coupling is developed. The in situ prepared three-component system Pd(OAC)(2)-1,3bis(alkyl)imidazolinium chlorides (2a-f) and CS2CO3 catalyses quantitatively the Suzuki crosscoupling of deactivated aryl chlorides. Copyright (C) 2004 John Wiley Sons, Ltd.eninfo:eu-repo/semantics/closedAccesspalladiumimidazolidin-2-ylidenearyl halidesphenylboronic acidSuzuki couplingPalladium-catalysed Suzuki reaction of aryl chlorides in aqueous media using 1,3-dialkylimidazolidin-2-ylidene ligandsArticle191555810.1002/aoc.7932-s2.0-12844271107Q2WOS:000226727800009Q2