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dc.contributor.authorFeofanov, Mikhail-
dc.contributor.authorAkhmetov, Vladimir-
dc.contributor.authorAmsharov, Konstantin-
dc.date.accessioned2021-09-29T10:06:13Z-
dc.date.available2021-09-29T10:06:13Z-
dc.date.issued2020-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/38772-
dc.identifier.urihttp://dx.doi.org/10.25673/38526-
dc.description.abstractAlumina-mediated C-F activation (AmCFA) is an established method to generate incipient phenyl cation (IPC) through polarization of C(aryl)-F bonds. Herein, it is reported that AmCFA can be used to induce intramolecular arylation of aryl alkynes containing one, two, and three triple bonds. During the reaction, a single formally eliminated hydrogen fluoride (HF) leads to the formation of two, three, and four C-C bonds, respectively. Thus, the transformation gives rapid access to π-extension and serves as an interesting example of solid-state rational domino annulation enabling the bottom-up construction of nanographenes.eng
dc.description.sponsorshipPublikationsfonds MLU-
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc546-
dc.titleAnnulation cascade of aryl alkynes induced by alumina-mediated C-F bond activationeng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitlePhysica status solidi / B-
local.bibliographicCitation.volume257-
local.bibliographicCitation.issue12-
local.bibliographicCitation.publishernameWiley-VCH-
local.bibliographicCitation.publisherplaceWeinheim-
local.bibliographicCitation.doi10.1002/pssb.202000296-
local.openaccesstrue-
local.accessrights.dnbfree-
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