Rhodium(i)-Catalyzed Carbonylative Arylation of Alkynes With Arylboronic Acids Using Formaldehyde as a Carbonyl Source

dc.contributor.author Wang, Chuang
dc.contributor.author Morimoto, Tsumoru
dc.contributor.author Kanashiro, Hiroyuki
dc.contributor.author Tanimoto, Hiroki
dc.contributor.author Nishiyama, Yasuhiro
dc.contributor.author Kakiuchi, Kiyomi
dc.contributor.author Artok, Levent
dc.coverage.doi 10.1055/s-0033-1341046
dc.date.accessioned 2018-02-20T13:20:35Z
dc.date.available 2018-02-20T13:20:35Z
dc.date.issued 2014
dc.description.abstract The 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.sponsorship Ministry of Education, Culture, Sports, Science and Technology, Japan en_US
dc.identifier.citation Wang, 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-0033-1341046 en_US
dc.identifier.doi 10.1055/s-0033-1341046 en_US
dc.identifier.doi 10.1055/s-0033-1341046
dc.identifier.issn 0936-5214
dc.identifier.issn 1437-2096
dc.identifier.scopus 2-s2.0-84899923051
dc.identifier.uri http://doi.org/10.1055/s-0033-1341046
dc.identifier.uri https://hdl.handle.net/11147/6814
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 Arylation en_US
dc.subject Carbonylation en_US
dc.subject Formaldehyde en_US
dc.subject Rhodium en_US
dc.title Rhodium(i)-Catalyzed Carbonylative Arylation of Alkynes With Arylboronic Acids Using Formaldehyde as a Carbonyl Source en_US
dc.type Article en_US
dspace.entity.type Publication
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 1159 en_US
gdc.description.issue 8 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 1155 en_US
gdc.description.volume 25 en_US
gdc.description.wosquality Q3
gdc.identifier.openalex W2319170611
gdc.identifier.wos WOS:000335152300022
gdc.index.type WoS
gdc.index.type Scopus
gdc.oaire.accesstype BRONZE
gdc.oaire.diamondjournal false
gdc.oaire.impulse 4.0
gdc.oaire.influence 2.90913E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Alkynes
gdc.oaire.keywords Formaldehyde
gdc.oaire.keywords Carbonylation
gdc.oaire.keywords Rhodium
gdc.oaire.keywords Arylation
gdc.oaire.popularity 1.1034021E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 02 engineering and technology
gdc.oaire.sciencefields 0210 nano-technology
gdc.oaire.sciencefields 01 natural sciences
gdc.oaire.sciencefields 0104 chemical sciences
gdc.openalex.collaboration International
gdc.openalex.fwci 0.74445984
gdc.openalex.normalizedpercentile 0.72
gdc.opencitations.count 11
gdc.plumx.crossrefcites 4
gdc.plumx.mendeley 10
gdc.plumx.scopuscites 14
gdc.scopus.citedcount 14
gdc.wos.citedcount 13
relation.isAuthorOfPublication.latestForDiscovery c7537e1c-5910-4672-ae89-a15f732d837d
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4011-8abe-a4dfe192da5e

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