Synthesis of Α,β-Unsaturated Ketones by Rhodium-Catalyzed Carbonylative Arylation of Internal Alkynes With Arylboronic Acids

dc.contributor.author Kuş, Melih
dc.contributor.author Aksın Artok, Özge
dc.contributor.author Ziyanak, Fırat
dc.contributor.author Artok, Levent
dc.coverage.doi 10.1055/s-2008-1078047
dc.date.accessioned 2016-10-31T13:56:20Z
dc.date.available 2016-10-31T13:56:20Z
dc.date.issued 2008
dc.description.abstract The Rh-catalyzed reaction of arylboronic acids with internal alkynes under a CO atmosphere in the presence of an acid additive afforded α,β-unsaturated ketones as the major products. Hydroacylation of internal alkynes, except in the case of diaryl acetylenes, proceeded in syn fashion, yielding the E-configured isomer. A mixture of E- and Z-isomers was obtained with diphenyl acetylene. Reactions were also highly regioselective for various nonsymmetric alkynes. en_US
dc.description.sponsorship Scientific and Technical Research Council of Turkey (TBAG-106T385), National Boron Research Institute (BOREN-2006-14-Ç13-09), and IZTECH (2007-IYTE-14) en_US
dc.identifier.citation Kuş, M., Aksın Artok, Ö., Ziyanak, F., and Artok, L. (2008). Synthesis of α,β-unsaturated ketones by rhodium-catalyzed carbonylative arylation of internal alkynes with arylboronic acids. Synlett, (17), 2587-2592. en_US
dc.identifier.doi 10.1055/s-2008-1078047 en_US
dc.identifier.doi 10.1055/s-2008-1078047
dc.identifier.issn 0936-5214
dc.identifier.scopus 2-s2.0-55549108402
dc.identifier.uri https://hdl.handle.net/11147/2354
dc.identifier.uri http://doi.org/10.1055/s-2008-1078047
dc.language.iso en en_US
dc.publisher Georg Thieme Verlag en_US
dc.relation.ispartof Synlett en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Alkynes en_US
dc.subject Boron en_US
dc.subject Carbonylation en_US
dc.subject Enones en_US
dc.subject Rhodium en_US
dc.title Synthesis of Α,β-Unsaturated Ketones by Rhodium-Catalyzed Carbonylative Arylation of Internal Alkynes With Arylboronic Acids en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Kuş, Melih
gdc.author.institutional Aksın Artok, Özge
gdc.author.institutional Ziyanak, Fırat
gdc.author.institutional Artok, Levent
gdc.bip.impulseclass C5
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 2592 en_US
gdc.description.issue 17 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 2587 en_US
gdc.description.volume 2008
gdc.description.wosquality Q3
gdc.identifier.openalex W2951690640
gdc.identifier.wos WOS:000260777600005
gdc.index.type WoS
gdc.index.type Scopus
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.impulse 0.0
gdc.oaire.influence 2.6566669E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Alkynes
gdc.oaire.keywords Enones
gdc.oaire.keywords Carbonylation
gdc.oaire.keywords Rhodium
gdc.oaire.keywords Boron
gdc.oaire.popularity 4.2913786E-10
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 0.34577336
gdc.openalex.normalizedpercentile 0.63
gdc.opencitations.count 2
gdc.plumx.crossrefcites 2
gdc.plumx.mendeley 4
gdc.scopus.citedcount 2
gdc.wos.citedcount 11
relation.isAuthorOfPublication.latestForDiscovery bc684629-1a86-4ac8-923b-3217fe31b341
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4011-8abe-a4dfe192da5e

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