Pd-N-Heterocyclic carbene catalysed Suzuki-Miyaura coupling reactions in aqueous medium
dc.authorid | Yaşar, Sedat/0000-0001-7285-2761 | |
dc.authorid | Özdemir, İsmail/0000-0001-6325-0216 | |
dc.authorid | AKKOÇ, Mitat/0000-0001-8641-8958 | |
dc.authorid | karaca, emine özge/0000-0003-2094-9742 | |
dc.authorwosid | Yaşar, Sedat/ABG-8356-2020 | |
dc.authorwosid | Özdemir, İsmail/ABI-5192-2020 | |
dc.authorwosid | AKKOÇ, Mitat/AAJ-5780-2020 | |
dc.authorwosid | karaca, emine özge/AAH-2535-2019 | |
dc.contributor.author | Karaca, Emine Ozge | |
dc.contributor.author | Akkoc, Mitat | |
dc.contributor.author | Yasar, Sedat | |
dc.contributor.author | Ozdemir, Ismail | |
dc.date.accessioned | 2024-08-04T20:45:23Z | |
dc.date.available | 2024-08-04T20:45:23Z | |
dc.date.issued | 2018 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | A new series of methyl substituted imidazole-based N-heterocyclic carbene (NHC) palladium complexes (PdCl2(L-1)NHC(L-1 =pyridine) is reported. Structural definitions of Pd-PEPPSI complexes were determined by NMR spectroscopy, elemental analysis and LC-MS spectroscopy techniques. To evolve a more efficient catalytic system for electronically different aryl chloride substrates on the Suzuki cross-coupling reaction, complexes were used as pre-catalyst. Activity of palladium(II)-NHC complexes screened under mild reaction conditions in aqueous media. With this catalytic system, the reaction proceeded in moderate or good yields with low catalyst loading (0.1 mol%). [GRAPHICS] . | en_US |
dc.description.sponsorship | Inonu University Research Fund [BAP: 2016-195] | en_US |
dc.description.sponsorship | This work was financially supported by Inonu University Research Fund (BAP: 2016-195). | en_US |
dc.identifier.doi | 10.24820/ark.5550190.p010.519 | |
dc.identifier.endpage | 239 | en_US |
dc.identifier.issn | 1551-7004 | |
dc.identifier.issn | 1551-7012 | |
dc.identifier.scopus | 2-s2.0-85052635291 | en_US |
dc.identifier.scopusquality | Q4 | en_US |
dc.identifier.startpage | 230 | en_US |
dc.identifier.uri | https://doi.org/10.24820/ark.5550190.p010.519 | |
dc.identifier.uri | https://hdl.handle.net/11616/98449 | |
dc.identifier.wos | WOS:000456008800021 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Arkat Usa Inc | en_US |
dc.relation.ispartof | Arkivoc | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Suzuki-Miyaura cross-coupling reaction | en_US |
dc.subject | N-heterocyclic carbene | en_US |
dc.subject | Pd-PEPPSI complex | en_US |
dc.subject | C-C bond formation | en_US |
dc.title | Pd-N-Heterocyclic carbene catalysed Suzuki-Miyaura coupling reactions in aqueous medium | en_US |
dc.type | Article | en_US |