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

Filip S. Ekholm, Lucas Lagerquist, Reko Leino

    Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

    2 Citeringar (Scopus)

    Sammanfattning

    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.
    OriginalspråkOdefinierat/okänt
    Sidor (från-till)858–862
    Antal sidor5
    TidskriftCarbohydrate Research
    Volym346
    Utgåva6
    DOI
    StatusPublicerad - 2011
    MoE-publikationstypA1 Tidskriftsartikel-refererad

    Nyckelord

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

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