Synthesis of aryl-substituted quinolines and tetrahydroquinolines through Suzuki-Miyaura coupling reactions
dc.contributor.author | Ökten, Salih | |
dc.date.accessioned | 2020-06-25T18:34:00Z | |
dc.date.available | 2020-06-25T18:34:00Z | |
dc.date.issued | 2019 | |
dc.department | Kırıkkale Üniversitesi | |
dc.description | Okten, Salih/0000-0001-9656-1803 | |
dc.description.abstract | The synthesis and characterization of substituted (trifluoromethoxy, thiomethyl, and methoxy) phenyl quinolines is described. Dichlorobis(triphenylphosphine)palladiunn(II)-catalyzed Suzuki-Miyaura cross-coupling of 6-bromo- and 6,8-dibronno-1,2,3,4-tetrahydroquinolines, 5-bromo-8-methoxyquinoline, and 5,7-dibromo-8-methoxyquinoline with substituted phenylboronic acids affords the corresponding 6-aryl- (13a-d), 6,8-diaryl- (14a-c), 5-aryl- (15), and 5,7-diaryl- (16b, c) tetrahydroquinolines and quinolines in high yields (68%-82%). The structures of all the products are characterized by H-1 NMR, C-13 NMR, F-1(9) NMR, and Fourier transform infrared spectroscopy and by elemental analysis. | en_US |
dc.description.sponsorship | Scientific and Technological Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [112T394] | en_US |
dc.description.sponsorship | The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This study was supported by grants from the Scientific and Technological Research Council of Turkey (TUBITAK; project number: 112T394). | en_US |
dc.identifier.citation | closedAccess | en_US |
dc.identifier.doi | 10.1177/1747519819861389 | |
dc.identifier.endpage | 280 | en_US |
dc.identifier.issn | 1747-5198 | |
dc.identifier.issn | 2047-6507 | |
dc.identifier.issue | 7-8 | en_US |
dc.identifier.scopus | 2-s2.0-85070482400 | |
dc.identifier.scopusquality | Q3 | |
dc.identifier.startpage | 274 | en_US |
dc.identifier.uri | https://doi.org/10.1177/1747519819861389 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12587/7741 | |
dc.identifier.volume | 43 | en_US |
dc.identifier.wos | WOS:000484663600009 | |
dc.identifier.wosquality | Q4 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | |
dc.publisher | Sage Publications Ltd | en_US |
dc.relation.ispartof | Journal Of Chemical Research | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | aryl quinolines | en_US |
dc.subject | nuclear magnetic resonance spectroscopy | en_US |
dc.subject | quinolines | en_US |
dc.subject | substituted phenyls | en_US |
dc.subject | Suzuk-Miyaura cross-coupling | en_US |
dc.subject | tetrahydroquinolines | en_US |
dc.title | Synthesis of aryl-substituted quinolines and tetrahydroquinolines through Suzuki-Miyaura coupling reactions | en_US |
dc.type | Article |
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