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Benzylic imidazolidinium, 3,4,5,6-tetrahydropyrimidinium and

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dc.contributor.author Yasar, S
dc.contributor.author Ozdemir, I
dc.contributor.author Cetinkaya, B
dc.contributor.author Renaud, JL
dc.contributor.author Bruneau, C
dc.date.accessioned 2022-10-19T11:01:40Z
dc.date.available 2022-10-19T11:01:40Z
dc.date.issued 2008
dc.identifier.uri http://hdl.handle.net/11616/82695
dc.description.abstract Imidazoliidinium, 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).
dc.description.abstract C1 [Renaud, Jean-Luc; Bruneau, Christian] Univ Rennes, CNRS, UMR 6226, F-35042 Rennes, France.
dc.description.abstract [Yasar, Sedat; Oezdemir, Ismail] Inonu Univ, Fac Sci & Art, Dept Chem, TR-44069 Malatya, Turkey.
dc.description.abstract [Cetinkaya, Bekir] Ege Univ, Dept Chem, TR-35100 Izmir, Turkey.
dc.source EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
dc.title Benzylic imidazolidinium, 3,4,5,6-tetrahydropyrimidinium and
dc.title benzimidazolium salts: Applications in ruthenium-catalyzed allylic
dc.title substitution reactions


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