Heck coupling reactions of aryl halides catalyzed by saturated ferrocenylmethylimidazolinium salts/palladium

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dc.contributor.authorMusaoğlu D.
dc.contributor.authorAvcı Özbek H.
dc.contributor.authorDemirhan F.
dc.date.accessioned2024-07-22T08:03:08Z
dc.date.available2024-07-22T08:03:08Z
dc.date.issued2023
dc.description.abstractIn situ prepared Pd(OAc)2/N,N′-bis(ferrocenyl methyl) imidazolinium salt catalyst systems were successfully applied to Heck reactions of various aryl halides (bromides, iodides) with olefins (styrene, ethyl acrylate). Catalytic studies showed that N,N′-bis(ferrocenylmethyl)imidazolinium chloride containing a saturated imidazole ring as an auxiliary catalyst in the presence of Pd(OAc)2 was highly efficient in Heck coupling reaction of aryl halides in DMF. © 2022, Iranian Chemical Society.
dc.identifier.DOI-ID10.1007/s13738-022-02689-3
dc.identifier.issn1735207X
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/12150
dc.language.isoEnglish
dc.publisherSpringer Science and Business Media Deutschland GmbH
dc.titleHeck coupling reactions of aryl halides catalyzed by saturated ferrocenylmethylimidazolinium salts/palladium
dc.typeArticle

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