Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/2739
Full metadata record
DC FieldValueLanguage
dc.contributor.authorArtok, Levent-
dc.contributor.authorKuş, Melih-
dc.contributor.authorÜrer, Bağdagül N.-
dc.contributor.authorTürkmen, Gülşah-
dc.contributor.authorAksın Artok, Özge-
dc.date.accessioned2017-01-06T13:44:22Z-
dc.date.available2017-01-06T13:44:22Z-
dc.date.issued2010-
dc.identifier.citationArtok, 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/b926553hen_US
dc.identifier.issn1477-0520-
dc.identifier.issn1477-0539-
dc.identifier.urihttp://doi.org/10.1039/b926553h-
dc.identifier.urihttp://hdl.handle.net/11147/2739-
dc.description.abstractUnsymmetric 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.sponsorshipThe National Boron Research Institute (BOREN-2006-14-C, 13-09), and IZTECH (2007-IYTE-14)en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.ispartofOrganic and Biomolecular Chemistryen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectRhodiumen_US
dc.subjectCyclisationsen_US
dc.subjectOrganoboronic acidsen_US
dc.subjectProtic solventsen_US
dc.subjectTerminal alkyneen_US
dc.titleRhodium catalysed chemo- and stereoselective arylative and alkenylative cyclisation reactions of unsymmetric diynes containing a terminal alkyne moiety with organoboronic acidsen_US
dc.typeArticleen_US
dc.authoridTR1860en_US
dc.institutionauthorArtok, Levent-
dc.institutionauthorKuş, Melih-
dc.institutionauthorÜrer, Bağdagül N.-
dc.institutionauthorTürkmen, Gülşah-
dc.departmentİzmir Institute of Technology. Chemistryen_US
dc.identifier.volume8en_US
dc.identifier.issue9en_US
dc.identifier.startpage2060en_US
dc.identifier.endpage2067en_US
dc.identifier.wosWOS:000276786000012en_US
dc.identifier.scopus2-s2.0-77951143587en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1039/b926553h-
dc.identifier.pmid20401382en_US
dc.relation.doi10.1039/b926553hen_US
dc.coverage.doi10.1039/b926553hen_US
dc.identifier.wosqualityQ2-
dc.identifier.scopusqualityQ3-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
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 
2739.pdfMakale257.38 kBAdobe PDFThumbnail
View/Open
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

14
checked on Nov 15, 2024

WEB OF SCIENCETM
Citations

15
checked on Nov 9, 2024

Page view(s)

316
checked on Nov 18, 2024

Download(s)

290
checked on Nov 18, 2024

Google ScholarTM

Check




Altmetric


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