Stereo- and regioselective glycosylation of 4-deoxy-epsilon-rhodomycinone

Filip S. Ekholm, Lucas Lagerquist, Reko Leino

    Tutkimustuotos: LehtiartikkeliArtikkeliTieteellinenvertaisarvioitu

    2 Sitaatiot (Scopus)

    Abstrakti

    A method for the glycosylation of anthracyclines featuring benzoylated imidate donors has been developed and utilized in the synthesis of glycosylated 4-deoxy-epsilon-rhodomycinone derivatives. Due to its high efficiency, regioselectivity, stereoselectivity, and operational simplicity, the method should prove valuable to researchers working with glycosylation of tetracyclic compounds. (C) 2011 Elsevier Ltd. All rights reserved.
    AlkuperäiskieliEi tiedossa
    Sivut858–862
    Sivumäärä5
    JulkaisuCarbohydrate Research
    Vuosikerta346
    Numero6
    DOI - pysyväislinkit
    TilaJulkaistu - 2011
    OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

    Keywords

    • Anthracycline
    • Glycosylation
    • Regioselectivite synthesis
    • Rhodomycinone glycosides
    • Stereoselective synthesis

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