Palladium-Catalysed Reactions of Conjugated Enyne Oxiranes With Organoborons: a Diastereoselective Method of the Synthesis of 2,4,5-Trienol Derivatives
| dc.contributor.author | Ziyanak, Fırat | |
| dc.contributor.author | Kuş, Melih | |
| dc.contributor.author | Alkan Karadeniz, Leman | |
| dc.contributor.author | Artok, Levent | |
| dc.coverage.doi | 10.1016/j.tet.2018.05.030 | |
| dc.date.accessioned | 2020-01-21T12:41:54Z | |
| dc.date.available | 2020-01-21T12:41:54Z | |
| dc.date.issued | 2017 | |
| dc.description.abstract | A palladium-catalysed reaction of conjugated enyne oxiranes with organoboron reagents is described. This method allows aryl-substituted vinylallenes containing a hydroxyl group on the allylic position to be synthesized, with good diastereomeric ratios, under mild conditions. | en_US |
| dc.description.sponsorship | The Scientific and Technological Research Council of Turkey and Federal Ministry of Education and Research (Germany) via the Intensified Cooperation Program (201T092) | en_US |
| dc.identifier.citation | Ziyanak, F., Kuş, M., Alkan Karadeniz, L., and Artok, L. (2018). Palladium-catalysed reactions of conjugated enyne oxiranes with organoborons: A diastereoselective method of the synthesis of 2,4,5-trienol derivatives. Tetrahedron, 74(27), 3652-3662. doi:10.1016/j.tet.2018.05.030 | en_US |
| dc.identifier.doi | 10.1016/j.tet.2018.05.030 | |
| dc.identifier.doi | 10.1016/j.tet.2018.05.030 | en_US |
| dc.identifier.issn | 0040-4020 | |
| dc.identifier.issn | 1464-5416 | |
| dc.identifier.scopus | 2-s2.0-85047074540 | |
| dc.identifier.uri | https://doi.org/10.1016/j.tet.2018.05.030 | |
| dc.identifier.uri | https://hdl.handle.net/11147/7610 | |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier | en_US |
| dc.relation | 2-4-Eninlerin Geçiş Metal Katalizli Alkoksikarbonilasyon ve C-C Kenetlenme Tepkimeleri, Oluşan Fonksiyonel Vinilalen Ürünlerin Altın Katalizli Tepkimeleri | |
| dc.relation.ispartof | Tetrahedron | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Enyne oxirane | en_US |
| dc.subject | Organoboron | en_US |
| dc.subject | Vinylallene | en_US |
| dc.subject | 2,4,5-Trienol | en_US |
| dc.subject | Allene derivative | en_US |
| dc.title | Palladium-Catalysed Reactions of Conjugated Enyne Oxiranes With Organoborons: a Diastereoselective Method of the Synthesis of 2,4,5-Trienol Derivatives | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| gdc.author.id | 0000-0003-4678-4819 | |
| gdc.author.id | 0000-0003-4678-4819 | en_US |
| gdc.author.institutional | Ziyanak, Fırat | |
| gdc.author.institutional | Kuş, Melih | |
| gdc.author.institutional | Artok, Levent | |
| gdc.bip.impulseclass | C4 | |
| gdc.bip.influenceclass | C5 | |
| gdc.bip.popularityclass | C4 | |
| gdc.coar.access | open access | |
| gdc.coar.type | text::journal::journal article | |
| gdc.collaboration.industrial | false | |
| gdc.description.department | İzmir Institute of Technology. Chemistry | en_US |
| gdc.description.endpage | 3662 | en_US |
| gdc.description.issue | 27 | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| gdc.description.scopusquality | Q3 | |
| gdc.description.startpage | 3652 | en_US |
| gdc.description.volume | 74 | en_US |
| gdc.description.wosquality | Q2 | |
| gdc.identifier.openalex | W2802397177 | |
| gdc.identifier.wos | WOS:000436218100022 | |
| gdc.index.type | WoS | |
| gdc.index.type | Scopus | |
| gdc.oaire.accesstype | BRONZE | |
| gdc.oaire.diamondjournal | false | |
| gdc.oaire.downloads | 2 | |
| gdc.oaire.impulse | 5.0 | |
| gdc.oaire.influence | 2.7215596E-9 | |
| gdc.oaire.isgreen | true | |
| gdc.oaire.keywords | Allene derivative | |
| gdc.oaire.keywords | Allene | |
| gdc.oaire.keywords | Enyne oxirane | |
| gdc.oaire.keywords | 2,4,5-Trienol | |
| gdc.oaire.keywords | Organoboron | |
| gdc.oaire.keywords | Vinylallene | |
| gdc.oaire.popularity | 5.109329E-9 | |
| gdc.oaire.publicfunded | false | |
| gdc.oaire.sciencefields | 01 natural sciences | |
| gdc.oaire.sciencefields | 0104 chemical sciences | |
| gdc.oaire.views | 2 | |
| gdc.openalex.collaboration | National | |
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| gdc.openalex.normalizedpercentile | 0.63 | |
| gdc.opencitations.count | 6 | |
| gdc.plumx.crossrefcites | 7 | |
| gdc.plumx.mendeley | 5 | |
| gdc.plumx.scopuscites | 6 | |
| gdc.relation.tubitak | info:eu-repo/grantAgreement/TUBITAK/TBAG/201T092 | |
| gdc.scopus.citedcount | 6 | |
| gdc.wos.citedcount | 6 | |
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