Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/5889
Full metadata record
DC FieldValueLanguage
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-hydroxy-2,3,5-trienoatesen_US
dc.typeArticleen_US
dc.authoridTR1860en_US
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:000355962300012en_US
dc.identifier.scopus2-s2.0-84930625632en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1021/acs.joc.5b00382-
dc.identifier.pmid25912857en_US
dc.relation.doi10.1021/acs.joc.5b00382en_US
dc.coverage.doi10.1021/acs.joc.5b00382en_US
dc.identifier.wosqualityQ1-
dc.identifier.scopusqualityQ1-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.grantfulltextopen-
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
Files in This Item:
File Description SizeFormat 
5889.pdfMakale877.97 kBAdobe PDFThumbnail
View/Open
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

20
checked on Mar 22, 2024

WEB OF SCIENCETM
Citations

20
checked on Mar 23, 2024

Page view(s)

170
checked on Mar 25, 2024

Download(s)

282
checked on Mar 25, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.