Silylium-ion-promoted (5+1) cycloaddition of aryl-substituted vinylcyclopropanes and hydrosilanes involving aryl migration

dc.contributor.authorHe, Tao
dc.contributor.authorWang, Guoqiang
dc.contributor.authorBonetti, Vittorio
dc.contributor.authorKlare, Hendrik F. T.
dc.contributor.authorOestreich, Martin
dc.date.accessioned2021-06-03T14:09:22Z
dc.date.available2021-06-03T14:09:22Z
dc.date.issued2020-04-17
dc.description.abstractA transition-metal-free (5+1) cycloaddition of aryl-substituted vinylcyclopropanes (VCPs) and hydrosilanes to afford silacyclohexanes is reported. Catalytic amounts of the trityl cation initiate the reaction by hydride abstraction from the hydrosilane, and further progress of the reaction is maintained by self-regeneration of the silylium ions. The new reaction involves a [1,2] migration of an aryl group, eventually furnishing 4- rather than 3-aryl-substituted silacyclohexane derivatives as major products. Various control experiments and quantum-chemical calculations support a mechanistic picture where a silylium ion intramolecularly stabilized by a cyclopropane ring can either undergo a kinetically favored concerted [1,2] aryl migration/ring expansion or engage in a cyclopropane-to-cyclopropane rearrangement.en
dc.description.sponsorshipDFG, 390540038, EXC 2008: Unifying Systems in Catalysis "UniSysCat"en
dc.description.sponsorshipTU Berlin, Open-Access-Mittel – 2020en
dc.identifier.eissn1521-3757
dc.identifier.issn0044-8249
dc.identifier.urihttps://depositonce.tu-berlin.de/handle/11303/13196
dc.identifier.urihttp://dx.doi.org/10.14279/depositonce-11991
dc.language.isoenen
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en
dc.subject.ddc547 Organische Chemiede
dc.subject.othercycloadditionen
dc.subject.otherdensity-functional calculationsen
dc.subject.otherring expansionen
dc.subject.othersilylium ionsen
dc.subject.othersmall-ring systemsen
dc.titleSilylium-ion-promoted (5+1) cycloaddition of aryl-substituted vinylcyclopropanes and hydrosilanes involving aryl migrationen
dc.typeArticleen
dc.type.versionpublishedVersionen
dcterms.bibliographicCitation.doi10.1002/anie.202004320en
dcterms.bibliographicCitation.issue29en
dcterms.bibliographicCitation.journaltitleAngewandte Chemieen
dcterms.bibliographicCitation.originalpublishernameWileyen
dcterms.bibliographicCitation.originalpublisherplaceNew York, NYen
dcterms.bibliographicCitation.pageend12191en
dcterms.bibliographicCitation.pagestart12186en
dcterms.bibliographicCitation.volume59en
tub.accessrights.dnbfreeen
tub.affiliationFak. 2 Mathematik und Naturwissenschaften::Inst. Chemie::FG Organische Chemie / Synthese und Katalysede
tub.affiliation.facultyFak. 2 Mathematik und Naturwissenschaftende
tub.affiliation.groupFG Organische Chemie / Synthese und Katalysede
tub.affiliation.instituteInst. Chemiede
tub.publisher.universityorinstitutionTechnische Universität Berlinen

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