Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/6814
Full metadata record
DC FieldValueLanguage
dc.contributor.authorWang, Chuang-
dc.contributor.authorMorimoto, Tsumoru-
dc.contributor.authorKanashiro, Hiroyuki-
dc.contributor.authorTanimoto, Hiroki-
dc.contributor.authorNishiyama, Yasuhiro-
dc.contributor.authorKakiuchi, Kiyomi-
dc.contributor.authorArtok, Levent-
dc.date.accessioned2018-02-20T13:20:35Z-
dc.date.available2018-02-20T13:20:35Z-
dc.date.issued2014-05-
dc.identifier.citationWang, C., Morimoto, T., Kanashiro, H., Tanimoto, H., Nishiyama, Y., Kakiuchi, K., and Artok, L. (2014). Rhodium(I)-catalyzed carbonylative arylation of alkynes with arylboronic acids using formaldehyde as a carbonyl source. Synlett, 25(8), 1155-1159. doi:10.1055/s-0033-1341046en_US
dc.identifier.issn0936-5214-
dc.identifier.urihttp://doi.org/10.1055/s-0033-1341046-
dc.identifier.urihttp://hdl.handle.net/11147/6814-
dc.description.abstractThe rhodium(I)-catalyzed reaction of alkynes with arylboronic acids in the presence of formaldehyde resulted in a carbon monoxide gas-free carbonylative arylation to yield α,β-enones. The simultaneous loading of phosphine-ligated and phosphine-free rhodium(I) complexes is required for efficient catalysis, which catalyze the abstraction of a carbonyl moiety from formaldehyde (decarbonylation) and its subsequent introduction into the substrate (carbonylation), respectively.en_US
dc.description.sponsorshipMinistry of Education, Culture, Sports, Science and Technology, Japanen_US
dc.language.isoenen_US
dc.publisherGeorg Thieme Verlagen_US
dc.relation.ispartofSynletten_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAlkynesen_US
dc.subjectArylationen_US
dc.subjectCarbonylationen_US
dc.subjectFormaldehydeen_US
dc.subjectRhodiumen_US
dc.titleRhodium(I)-catalyzed carbonylative arylation of alkynes with arylboronic acids using formaldehyde as a carbonyl sourceen_US
dc.typeArticleen_US
dc.authoridTR1860en_US
dc.institutionauthorArtok, Levent-
dc.departmentİzmir Institute of Technology. Chemistryen_US
dc.identifier.volume25en_US
dc.identifier.issue8en_US
dc.identifier.startpage1155en_US
dc.identifier.endpage1159en_US
dc.identifier.wosWOS:000335152300022en_US
dc.identifier.scopus2-s2.0-84899923051en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1055/s-0033-1341046-
dc.relation.doi10.1055/s-0033-1341046en_US
dc.coverage.doi10.1055/s-0033-1341046en_US
dc.identifier.wosqualityQ2-
dc.identifier.scopusqualityQ2-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.cerifentitytypePublications-
crisitem.author.dept04.01. Department of Chemistry-
Appears in Collections:Chemistry / Kimya
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Files in This Item:
File Description SizeFormat 
6814.pdfMakale200.37 kBAdobe PDFThumbnail
View/Open
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

13
checked on Apr 5, 2024

WEB OF SCIENCETM
Citations

13
checked on Apr 26, 2024

Page view(s)

184
checked on Apr 29, 2024

Download(s)

202
checked on Apr 29, 2024

Google ScholarTM

Check




Altmetric


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