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Ruthenium(II)-NHC-catalyzed (NHC = perhydrobenzimidazol-2-ylidene) alkylation of amines using the hydrogen borrowing methodology under solvent-free conditions

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dc.contributor.author Yiğit, Murat
dc.contributor.author Karaca, Emine Özge
dc.contributor.author Yiğit, Beyhan
dc.contributor.author Gürbüz, Nevin
dc.contributor.author Özdemir, İmail
dc.date.accessioned 2025-02-24T08:21:37Z
dc.date.available 2025-02-24T08:21:37Z
dc.date.issued 2019
dc.identifier.issn 0340-4285
dc.identifier.uri http://dspace.adiyaman.edu.tr:8080/xmlui/handle/20.500.12414/5830
dc.description.abstract New ruthenium(II) complexes with N-heterocyclic carbene ligand were synthesized by transmetalation reactions between silver(I) N-heterocyclic carbene complexes and [RuCl2(p-cymene)](2). The complexes were characterized by physicochemical and spectroscopic methods. These ruthenium complexes were applied to the N-monoalkylation of aromatic amines with a wide range of primary alcohols under solvent-free conditions using the hydrogen borrowing strategy. The catalytic reactions using all ruthenium complexes resulted in N-monoalkylated products with high selectivities using furfuryl alcohol as the alkylating agent. tr
dc.language.iso en tr
dc.publisher SPRINGER tr
dc.subject HETEROCYCLIC CARBENE COMPLEXES tr
dc.subject CATALYZED N-ALKYLATION tr
dc.subject SECONDARY ALCOHOLS tr
dc.subject SALTS tr
dc.subject HECK tr
dc.title Ruthenium(II)-NHC-catalyzed (NHC = perhydrobenzimidazol-2-ylidene) alkylation of amines using the hydrogen borrowing methodology under solvent-free conditions tr
dc.type Article tr
dc.contributor.authorID 0000-0003-2094-9742 tr
dc.contributor.authorID 0000-0003-3201-3597 tr
dc.contributor.department Adiyaman Univ, Fac Sci & Art, Dept Chem tr
dc.contributor.department Inonu Univ, Catalysis Res & Applicat Ctr tr
dc.contributor.department Inonu Univ, Fac Sci & Art, Dept Chem, tr
dc.identifier.endpage 573 tr
dc.identifier.issue 6 tr
dc.identifier.startpage 565 tr
dc.identifier.volume 44 tr
dc.source.title TRANSITION METAL CHEMISTRY tr


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