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Benzimidazolin-2-ylidene-palladium-catalysed coupling reactions of aryl

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dc.contributor.author Gok, Y
dc.contributor.author Gurbuz, N
dc.contributor.author Ozdemir, I
dc.contributor.author Cetinkaya, B
dc.contributor.author Cetinkaya, E
dc.date.accessioned 2022-10-19T12:10:35Z
dc.date.available 2022-10-19T12:10:35Z
dc.date.issued 2005
dc.identifier.uri http://hdl.handle.net/11616/83844
dc.description.abstract The in situ prepared three-component system Pd(OAC)(2)-1,3-dialkylbenzimidazolium chlorides (2a-f) and CS2CO3 catalyses, quantitatively, the Suzuki cross-coupling of deactivated aryl chlorides and Heck coupling reactions of aryl bromide and iodide substrates. The 1,3-dialkylbenzimidazolium salts (2a-f) were characterized by conventional spectroscopic methods and elemental analysis. Copyright (c) 2005 John Wiley & Sons, Ltd.
dc.description.abstract C1 Inonu Univ, Fac Sci & Arts, Dept Chem, Malatya 44280, Turkey.
dc.description.abstract Ege Univ, Dept Chem, TR-35100 Izmir, Turkey.
dc.source APPLIED ORGANOMETALLIC CHEMISTRY
dc.title Benzimidazolin-2-ylidene-palladium-catalysed coupling reactions of aryl
dc.title halides


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