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 Aygün, Muhittin
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
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gdc.oaire.accesstype BRONZE
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gdc.oaire.impulse 15.0
gdc.oaire.influence 3.1908833E-9
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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
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gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
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gdc.opencitations.count 21
gdc.plumx.crossrefcites 19
gdc.plumx.mendeley 12
gdc.plumx.scopuscites 21
gdc.scopus.citedcount 21
gdc.wos.citedcount 21
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