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Reactions of Nitroarenes with Corey-Chaykovsky Reagents

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cris.lastimport.scopus2024-02-12T20:44:52Z
dc.abstract.enElectrophilic and nucleophilic substitutions of aromatic substrates share common mechanistic pathways. In both scenarios reacting species attack rings at the unsubstituted (C-H) positions, giving cationic Wheland intermediates, or anionic Meisenheimer complexes. However, the following step of rearomatization breaks the intrinsic symmetry, due to different leaving group ability of proton and hydride anion, respectively. In effect, electron-deficient arenes are prone to transformations unparalleled in electrophilic chemistry. In our article, we present transformations of anionic σ H-adducts, formed between nitroarenes and carbanions of the Corey-Chaykowsky reagents. Depending on structure of the substrates and reaction conditions, the intermediates undergo cyclization to cyclopropanes (benzonorcaradienes), or base-induced elimination to the alkylated products. Mechanistic studies reveal that order of the carbanions controls competition between the processes, due to steric hindrance developing at the β-elimination step.
dc.affiliationUniwersytet Warszawski
dc.contributor.authorBarbasiewicz, Michał
dc.contributor.authorAntoniak, Damian
dc.date.accessioned2024-01-25T18:47:02Z
dc.date.available2024-01-25T18:47:02Z
dc.date.issued2023
dc.description.financePublikacja bezkosztowa
dc.description.volume34
dc.identifier.doi10.1055/A-1934-1254
dc.identifier.issn0936-5214
dc.identifier.urihttps://repozytorium.uw.edu.pl//handle/item/117900
dc.identifier.weblinkhttp://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1934-1254.pdf
dc.languageeng
dc.pbn.affiliationchemical sciences
dc.relation.ispartofSynlett
dc.relation.pages101-105
dc.rightsClosedAccess
dc.sciencecloudnosend
dc.subject.enAlkylation
dc.subject.enCarbanions
dc.subject.enCyclopropanation
dc.subject.enMeisenheimer complex
dc.subject.enNitroarenes
dc.subject.enSelenones
dc.subject.enSulfones
dc.subject.enSulfonium salts
dc.titleReactions of Nitroarenes with Corey-Chaykovsky Reagents
dc.typeJournalArticle
dspace.entity.typePublication