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In-situ generated 1-alkylimidazoline-palladium catalyst for the Suzuki

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dc.contributor.author Ozdemir, I
dc.contributor.author Sahin, N
dc.contributor.author Gurbuz, N
dc.contributor.author Demir, S
dc.contributor.author Gok, Y
dc.contributor.author Cetinkaya, B
dc.contributor.author Getinkaya, E
dc.date.accessioned 2022-10-19T12:10:34Z
dc.date.available 2022-10-19T12:10:34Z
dc.date.issued 2005
dc.identifier.uri http://hdl.handle.net/11616/83826
dc.description.abstract Five 1-alkyimidazoline (1-5) have been prepared and characterized by conventional spectroscopic methods and elemental analyses. New in situ generated palladium-imidazoline complexes were tested for catalytic activity in the Suzuki coupling reaction between phenylboronic acid and several aryl chlorides.
dc.description.abstract C1 Inonu Univ, Fac Sci & Art, Dept Chem, TR-44280 Malatya, Turkey.
dc.description.abstract Ege Univ, Dept Chem, Bornova, Turkey.
dc.source SYNTHESIS AND REACTIVITY IN INORGANIC METAL-ORGANIC AND NANO-METAL
dc.title In-situ generated 1-alkylimidazoline-palladium catalyst for the Suzuki
dc.title cross-coupling reaction of aryl chlorides


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