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Palladium-catalyzed Suzuki-Miyaura reaction using saturated

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dc.contributor.author Ozdemir, I
dc.contributor.author Cetinkaya, B
dc.contributor.author Demir, S
dc.contributor.author Gurbuz, N
dc.date.accessioned 2022-10-19T12:13:19Z
dc.date.available 2022-10-19T12:13:19Z
dc.date.issued 2004
dc.identifier.uri http://hdl.handle.net/11616/84084
dc.description.abstract The incorporation of saturated N-heterocyclic carbenes into palladium pre-catalysts give high catalyst activity in the Suzuki coupling of deactivated aryl chloride substrates.
dc.description.abstract [GRS]
dc.description.abstract The complexes were generated in the presence of Pd(OAc)(2) by in situ deprotonation of bis(imidazolinium) bromides LHX (3) which were characterized by conventional spectroscopic methods and elemental analyses.
dc.description.abstract C1 Inonu Univ, Dept Chem, TR-44069 Malatya, Turkey.
dc.description.abstract Ege Univ, Dept Chem, TR-35100 Bornova, Turkey.
dc.source CATALYSIS LETTERS
dc.title Palladium-catalyzed Suzuki-Miyaura reaction using saturated
dc.title N-heterocarbene ligands


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