Adamantane-derived aldo- and ketonitrones react with maleimides giving corresponding isoxazolidines. In the case of aldonitrones reactions proceed giving the diastereomeric mixtures. The ratio of isomers is changing during the reaction process due to the reversibility of the cycloaddition reaction. The cytotoxic and virus-inhibiting activity against influenza virus was investigated for selected adducts.

Original languageEnglish
Pages (from-to)1367-1374
Number of pages8
JournalSynthetic Communications
Volume50
Issue number9
Early online date18 Mar 2020
DOIs
StatePublished - 2 May 2020

    Research areas

  • Adamantane, antiviral activity, cycloaddition, isoxazolidines, nitrones, VIRUS, DIASTEREOSELECTIVITY, BIOLOGICAL EVALUATION, CHEMISTRY, ISOXAZOLIDINE, C-ARYLNITRONES

    Scopus subject areas

  • Organic Chemistry

ID: 52691953