Palladium-Catalyzed Alkoxycarbonylation of Conjugated Enyne Oxiranes: a Diastereoselective Method for the Synthesis of 7-Hydroxy
| dc.contributor.author | Kuş, Melih | |
| dc.contributor.author | Artok, Levent | |
| dc.contributor.author | Kuş, Melih | |
| dc.contributor.author | Artok, Levent | |
| dc.contributor.other | 04.01. Department of Chemistry | |
| dc.contributor.other | 04. Faculty of Science | |
| dc.contributor.other | 01. Izmir Institute of Technology | |
| dc.coverage.doi | 10.1021/acs.joc.5b00382 | |
| dc.date.accessioned | 2017-07-07T11:48:34Z | |
| dc.date.available | 2017-07-07T11:48:34Z | |
| dc.date.issued | 2015 | |
| dc.description.abstract | Palladium-catalyzed alkoxycarbonylative 1,5-substitution of conjugated enyne oxiranes provides a diastereoselective route to (E)-configured 7-hydroxy-2,3,5-trienoates. The reactions proceeded in a highly stereoselective manner, possibly through sequential formation of π-allylpalladium and σ-vinylallenyl palladium complexes. The major diastereomeric form of the product is determined by the configuration of the alkenyl moiety of the substrate. | en_US |
| dc.description.sponsorship | Federal Ministry of Education and Research (Germany) via Intensified Cooperation Program; Scientific and Technological Research Council of Turkey (210T092) | en_US |
| dc.identifier.citation | Kuş, M., Artok, L., and Aygün, M. (2015). Palladium-catalyzed alkoxycarbonylation of conjugated enyne oxiranes: A diastereoselective method for the synthesis of 7-hydroxy-2,3,5-trienoates. Journal of Organic Chemistry, 80(11), 5494-5506. doi:10.1021/acs.joc.5b00382 | en_US |
| dc.identifier.doi | 10.1021/acs.joc.5b00382 | |
| dc.identifier.doi | 10.1021/acs.joc.5b00382 | en_US |
| dc.identifier.issn | 0022-3263 | |
| dc.identifier.issn | 1520-6904 | |
| dc.identifier.scopus | 2-s2.0-84930625632 | |
| dc.identifier.uri | https://doi.org/10.1021/acs.joc.5b00382 | |
| dc.identifier.uri | https://hdl.handle.net/11147/5889 | |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.relation | info:eu-repo/grantAgreement/TUBITAK/TBAG/210T092 | en_US |
| dc.relation.ispartof | Journal of Organic Chemistry | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Catalysis | en_US |
| dc.subject | Palladium compounds | en_US |
| dc.subject | Stereoselectivity | en_US |
| dc.subject | Alkoxycarbonylation | en_US |
| dc.subject | Diastereoselective | en_US |
| dc.title | Palladium-Catalyzed Alkoxycarbonylation of Conjugated Enyne Oxiranes: a Diastereoselective Method for the Synthesis of 7-Hydroxy | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| gdc.author.institutional | Kuş, Melih | |
| gdc.author.institutional | Artok, Levent | |
| gdc.bip.impulseclass | C4 | |
| gdc.bip.influenceclass | C5 | |
| gdc.bip.popularityclass | C5 | |
| 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 | 5506 | en_US |
| gdc.description.issue | 11 | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| gdc.description.scopusquality | Q2 | |
| gdc.description.startpage | 5494 | en_US |
| gdc.description.volume | 80 | en_US |
| gdc.description.wosquality | Q1 | |
| gdc.identifier.openalex | W4241187106 | |
| gdc.identifier.pmid | 25912857 | |
| gdc.identifier.wos | WOS:000355962300012 | |
| gdc.index.type | WoS | |
| gdc.index.type | Scopus | |
| gdc.index.type | PubMed | |
| gdc.oaire.accesstype | BRONZE | |
| gdc.oaire.diamondjournal | false | |
| gdc.oaire.impulse | 15.0 | |
| gdc.oaire.influence | 3.1908833E-9 | |
| gdc.oaire.isgreen | true | |
| gdc.oaire.keywords | Palladium compounds | |
| gdc.oaire.keywords | Diastereoselective | |
| gdc.oaire.keywords | Stereoselectivity | |
| gdc.oaire.keywords | Catalysis | |
| gdc.oaire.keywords | Alkoxycarbonylation | |
| gdc.oaire.popularity | 4.22913E-9 | |
| gdc.oaire.publicfunded | false | |
| gdc.oaire.sciencefields | 01 natural sciences | |
| gdc.oaire.sciencefields | 0104 chemical sciences | |
| gdc.openalex.collaboration | National | |
| gdc.openalex.fwci | 2.32350135 | |
| gdc.openalex.normalizedpercentile | 0.9 | |
| gdc.openalex.toppercent | TOP 10% | |
| gdc.opencitations.count | 21 | |
| gdc.plumx.crossrefcites | 19 | |
| gdc.plumx.mendeley | 12 | |
| gdc.plumx.scopuscites | 21 | |
| gdc.scopus.citedcount | 21 | |
| gdc.wos.citedcount | 21 | |
| relation.isAuthorOfPublication | 79cee552-68b8-4a37-bad1-950c3fa5bd2f | |
| relation.isAuthorOfPublication | c7537e1c-5910-4672-ae89-a15f732d837d | |
| relation.isAuthorOfPublication.latestForDiscovery | 79cee552-68b8-4a37-bad1-950c3fa5bd2f | |
| relation.isOrgUnitOfPublication | 9af2b05f-28ac-4011-8abe-a4dfe192da5e | |
| relation.isOrgUnitOfPublication | 9af2b05f-28ac-4005-8abe-a4dfe193da5e | |
| relation.isOrgUnitOfPublication | 9af2b05f-28ac-4003-8abe-a4dfe192da5e | |
| relation.isOrgUnitOfPublication.latestForDiscovery | 9af2b05f-28ac-4011-8abe-a4dfe192da5e |