Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/5889
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dc.contributor.authorKuş, Melih-
dc.contributor.authorArtok, Levent-
dc.contributor.authorAygün, Muhittin-
dc.date.accessioned2017-07-07T11:48:34Z-
dc.date.available2017-07-07T11:48:34Z-
dc.date.issued2015-06-05-
dc.identifier.citationKuş, 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.5b00382en_US
dc.identifier.issn0022-3263-
dc.identifier.urihttps://doi.org/10.1021/acs.joc.5b00382-
dc.identifier.urihttp://hdl.handle.net/11147/5889-
dc.description.abstractPalladium-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.sponsorshipFederal Ministry of Education and Research (Germany) via Intensified Cooperation Program; Scientific and Technological Research Council of Turkey (210T092)en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.relationinfo:eu-repo/grantAgreement/TUBITAK/TBAG/210T092en_US
dc.relation.ispartofJournal of Organic Chemistryen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCatalysisen_US
dc.subjectPalladium compoundsen_US
dc.subjectStereoselectivityen_US
dc.subjectAlkoxycarbonylationen_US
dc.subjectDiastereoselectiveen_US
dc.titlePalladium-Catalyzed Alkoxycarbonylation of Conjugated Enyne Oxiranes: a Diastereoselective Method for the Synthesis of 7-Hydroxyen_US
dc.typeArticleen_US
dc.authoridTR1860-
dc.institutionauthorKuş, Melih-
dc.institutionauthorArtok, Levent-
dc.departmentİzmir Institute of Technology. Chemistryen_US
dc.identifier.volume80en_US
dc.identifier.issue11en_US
dc.identifier.startpage5494en_US
dc.identifier.endpage5506en_US
dc.identifier.wosWOS:000355962300012-
dc.identifier.scopus2-s2.0-84930625632-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1021/acs.joc.5b00382-
dc.identifier.pmid25912857-
dc.relation.doi10.1021/acs.joc.5b00382en_US
dc.coverage.doi10.1021/acs.joc.5b00382-
dc.identifier.wosqualityQ1-
dc.identifier.scopusqualityQ2-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
crisitem.author.dept04.01. Department of Chemistry-
crisitem.author.dept04.01. Department of Chemistry-
Appears in Collections:Chemistry / Kimya
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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