Platinum Catalyzed Ring-Opening of 1,2-Cyclopropanated Sugars with O-Nucleophiles

Jürgen Beyer, Philip Robert Skaanderup, Robert Madsen

    Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearch

    Abstract

    In the presence of a catalytic amount of Zeise's dimer 1,2-cyclopropanated sugars undergo regioselective ring-opening at C-1 with O-nucleophiles including alcohols, phenols and water to produce 2-C-branched carbohydrates.
    Original languageEnglish
    Title of host publicationOMCOS 10
    Place of PublicationVersailles
    PublisherMinistére de l'Education Nationale de la Recherche et de la Technologie
    Publication date1999
    Publication statusPublished - 1999
    Event10th IUPAC Symposium on Organo-Metallic Chemistry Directed Towards Organic Synthesis - Versailles, France
    Duration: 18 Jul 199922 Jul 1999
    Conference number: 10

    Conference

    Conference10th IUPAC Symposium on Organo-Metallic Chemistry Directed Towards Organic Synthesis
    Number10
    Country/TerritoryFrance
    CityVersailles
    Period18/07/199922/07/1999

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