Yasar, SedatOezdemir, IsmailCetinkaya, BekirRenaud, Jean-LucBruneau, Christian2024-08-042024-08-0420081434-193X1099-0690https://doi.org/10.1002/ejoc.200800007https://hdl.handle.net/11616/94668Imidazoliidinium, tetrahydropyrimidinium and benzimidazolium. salts were prepared. Upon reaction with tBuOK, they generate carbene ligands, which were associated in situ to [RuCp*(MeCN)(3)]PF6 to produce ruthenium catalysts that are active for the substitution of allylic substrates by dimethyl of the N-heterocyclic structures, as well as that of the benzyhc N-substituents, on the reactivity and regioselectivity were examined. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).eninfo:eu-repo/semantics/closedAccesscarbene ligandsnitrogen heterocyclesrutheniumallylationhomogeneous catalysisArticle2008122142214910.1002/ejoc.2008000072-s2.0-53749102171Q2WOS:000255508600015Q1