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Heck and suzuki reactions of aryl halides catalyzed by

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dc.contributor.author Yasar, S
dc.contributor.author Ozdemir, I
dc.contributor.author Cetinkaya, B
dc.date.accessioned 2022-10-19T11:01:31Z
dc.date.available 2022-10-19T11:01:31Z
dc.date.issued 2008
dc.identifier.uri http://hdl.handle.net/11616/82561
dc.description.abstract New, sterically demanding 1,3-dialkylimidazolinium salts used as N-heterocyclic carbene precursors were synthesized and characterized. These salts, combined with palladium acetate, provided active catalysts for Heck and suzuki cross-coupling of aryl chlorides and bromides under mild conditions.
dc.description.abstract C1 [Yasar, Sedat; Oezdemir, Ismail] Inonu Univ, Fac Sci & Arts, Dept Chem, TR-44280 Malatya, Turkey.
dc.description.abstract [Cetinkaya, Bekir] Ege Univ, Dept Chem, TR-35100 Bornova, Turkey.
dc.source CHINESE JOURNAL OF CATALYSIS
dc.title Heck and suzuki reactions of aryl halides catalyzed by
dc.title 1,3-dialkylimidazolinium/palladium


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