Potential N-Heterocyclic Carbene Precursors in the Palladium-Catalyzed Heck Reaction
dc.authorid | Düşünceli, Serpil Demir/0000-0001-8765-4039 | |
dc.authorid | Özdemir, İsmail/0000-0001-6325-0216 | |
dc.authorwosid | Düşünceli, Serpil Demir/AAA-7160-2021 | |
dc.authorwosid | Demir, Serpil/AAI-1740-2019 | |
dc.authorwosid | Özdemir, İsmail/ABI-5192-2020 | |
dc.contributor.author | Demir, Serpil | |
dc.contributor.author | Zengin, Rukiye | |
dc.contributor.author | Ozdemir, Ismail | |
dc.date.accessioned | 2024-08-04T20:37:23Z | |
dc.date.available | 2024-08-04T20:37:23Z | |
dc.date.issued | 2013 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | A novel 1-(cyclobutylmethyl)-substi-tuted imidazolidinium/benzimidazolium salts as N-heterocyclic carbene (NHC) precursors were successfully synthesized and characterized by 1H NMR, 13C NMR, IR, and elemental analysis techniques. These compounds were easily prepared from the reaction of N-alkyl imidazoline/N-alkyl benzimidazole with bromomethylcyclobutane in high yields. The in situ formed catalytic system derived from the NHC precursor and Pd(OAc)2 was used in the Heck reaction between aryl halides and styrene with potassium hydroxide in water. The corresponding Heck products were obtained in good yields. (c) 2012 Wiley Periodicals, Inc. Heteroatom Chem 24:7783, 2013; View this article online at wileyonlinelibrary.com. DOI 10.1002/hc.21065 | en_US |
dc.description.sponsorship | Inonu University Research Fund [IUBAP 2011/142] | en_US |
dc.description.sponsorship | Contract grant sponsor: Inonu University Research Fund.; Contract grant number: IUBAP 2011/142. | en_US |
dc.identifier.doi | 10.1002/hc.21065 | |
dc.identifier.endpage | 83 | en_US |
dc.identifier.issn | 1042-7163 | |
dc.identifier.issn | 1098-1071 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.scopus | 2-s2.0-84872263142 | en_US |
dc.identifier.scopusquality | Q4 | en_US |
dc.identifier.startpage | 77 | en_US |
dc.identifier.uri | https://doi.org/10.1002/hc.21065 | |
dc.identifier.uri | https://hdl.handle.net/11616/95919 | |
dc.identifier.volume | 24 | en_US |
dc.identifier.wos | WOS:000313592200011 | 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 | Wiley | en_US |
dc.relation.ispartof | Heteroatom Chemistry | 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 | Cross-Coupling Reaction | en_US |
dc.subject | Aryl Chlorides | en_US |
dc.subject | Aqueous-Media | en_US |
dc.subject | Olefin Metathesis | en_US |
dc.subject | Coordination Chemistry | en_US |
dc.subject | Benzimidazolium Salts | en_US |
dc.subject | Suzuki Reaction | en_US |
dc.subject | Water | en_US |
dc.subject | Ligands | en_US |
dc.subject | Complexes | en_US |
dc.title | Potential N-Heterocyclic Carbene Precursors in the Palladium-Catalyzed Heck Reaction | en_US |
dc.type | Article | en_US |