Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/121068
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dc.contributor.authorAlaoui, Nour-Eddine-
dc.contributor.authorAmsharov, Konstantin-
dc.date.accessioned2025-11-05T09:40:18Z-
dc.date.available2025-11-05T09:40:18Z-
dc.date.issued2025-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/123023-
dc.identifier.urihttp://dx.doi.org/10.25673/121068-
dc.description.abstractHerein, we demonstrate an unprecedentedly selective terminal bromination of fluorinated biphenylenes and oligophenylenes in the presence of excess metallic iron. The reaction can be carried out under ambient conditions at room temperature, yielding the target compounds with up to 98% yield. The high regioselectivity and scalability make this approach superior to existing methods.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc540-
dc.titleRegioselective terminal bromination of fluorinated oligophenyleneseng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleChemical communications-
local.bibliographicCitation.volume61-
local.bibliographicCitation.pagestart16194-
local.bibliographicCitation.pageend16197-
local.bibliographicCitation.publishernameSoc.-
local.bibliographicCitation.publisherplaceCambridge-
local.bibliographicCitation.doi10.1039/d5cc05074j-
local.openaccesstrue-
dc.identifier.ppn1940315972-
cbs.publication.displayform2025-
local.bibliographicCitation.year2025-
cbs.sru.importDate2025-11-05T09:39:51Z-
local.bibliographicCitationEnthalten in Chemical communications - Cambridge : Soc., 1965-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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