Rhodium Catalysed Chemo- and Stereoselective Arylative and Alkenylative Cyclisation Reactions of Unsymmetric Diynes Containing a Terminal Alkyne Moiety With Organoboronic Acids

dc.contributor.author Artok, Levent
dc.contributor.author Kuş, Melih
dc.contributor.author Ürer, Bağdagül N.
dc.contributor.author Türkmen, Gülşah
dc.contributor.author Aksın Artok, Özge
dc.coverage.doi 10.1039/b926553h
dc.date.accessioned 2017-01-06T13:44:22Z
dc.date.available 2017-01-06T13:44:22Z
dc.date.issued 2010
dc.description.abstract Unsymmetric diynes possessing a terminal alkyne moiety reacted with organoboronic acids both chemo- and stereoselectively to afford arylated or alkenylated exocyclic dienes by catalysis from the [Rh(cod)OCH 3] 2 complex. The use of a polar protic solvent, e.g. CH 3OH is required for the success of the process under mild conditions. © 2010 The Royal Society of Chemistry. en_US
dc.description.sponsorship The National Boron Research Institute (BOREN-2006-14-C, 13-09), and IZTECH (2007-IYTE-14) en_US
dc.identifier.citation Artok, L., Kuş, M., Ürer, B. N., Türkmen, G., and Aksın Artok, Ö. (2010). Rhodium catalysed chemo- and stereoselective arylative and alkenylative cyclisation reactions of unsymmetric diynes containing a terminal alkyne moiety with organoboronic acids. Organic and Biomolecular Chemistry, 8(9), 2060-2067. doi:10.1039/b926553h en_US
dc.identifier.doi 10.1039/b926553h en_US
dc.identifier.doi 10.1039/b926553h
dc.identifier.issn 1477-0520
dc.identifier.issn 1477-0539
dc.identifier.issn 0931-7597
dc.identifier.issn 1522-2667
dc.identifier.scopus 2-s2.0-77951143587
dc.identifier.uri http://doi.org/10.1039/b926553h
dc.identifier.uri https://hdl.handle.net/11147/2739
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.relation.ispartof Organic and Biomolecular Chemistry en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Rhodium en_US
dc.subject Cyclisations en_US
dc.subject Organoboronic acids en_US
dc.subject Protic solvents en_US
dc.subject Terminal alkyne en_US
dc.title Rhodium Catalysed Chemo- and Stereoselective Arylative and Alkenylative Cyclisation Reactions of Unsymmetric Diynes Containing a Terminal Alkyne Moiety With Organoboronic Acids en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Artok, Levent
gdc.author.institutional Kuş, Melih
gdc.author.institutional Ürer, Bağdagül N.
gdc.author.institutional Türkmen, Gülşah
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 2067 en_US
gdc.description.issue 9 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 2060 en_US
gdc.description.volume 8 en_US
gdc.description.wosquality Q2
gdc.identifier.openalex W2047316438
gdc.identifier.pmid 20401382
gdc.identifier.wos WOS:000276786000012
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.downloads 7
gdc.oaire.impulse 4.0
gdc.oaire.influence 3.1758418E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Cyclisations
gdc.oaire.keywords Molecular Structure
gdc.oaire.keywords Organoboronic acids
gdc.oaire.keywords Esters
gdc.oaire.keywords Stereoisomerism
gdc.oaire.keywords Terminal alkyne
gdc.oaire.keywords Boronic Acids
gdc.oaire.keywords Protic solvents
gdc.oaire.keywords Catalysis
gdc.oaire.keywords Alkadienes
gdc.oaire.keywords Cyclization
gdc.oaire.keywords Alkynes
gdc.oaire.keywords Organometallic Compounds
gdc.oaire.keywords Rhodium
gdc.oaire.popularity 3.863831E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.oaire.views 2
gdc.openalex.collaboration International
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gdc.openalex.normalizedpercentile 0.71
gdc.opencitations.count 16
gdc.plumx.crossrefcites 16
gdc.plumx.mendeley 7
gdc.plumx.pubmedcites 1
gdc.plumx.scopuscites 14
gdc.scopus.citedcount 14
gdc.wos.citedcount 15
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relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4011-8abe-a4dfe192da5e

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