Total Synthesis of the Antitumor Macrolides, (+)-Brefeldin A and 4‑Epi-Brefeldin A from D‑Glucose: Use of the Padwa Anionic Allenylsulfone [3+2]-Cycloadditive Elimination To Construct Trans-Configured Chiral Cyclopentane Systems

    Research output: Contribution to journalArticle

    Published

    View graph of relations

    A new synthesis of (+)-brefeldin A is reported via Padwa allenylsulfone [3+2]-cycloadditive elimination. Cycloadduct 13 was initially elaborated into iodide
    27, which, following treatment with Zn, gave aldehyde 28 whose C(9) stereocenter was epimerized. Further elaboration into enoate 38 and Julia−Kocienski olefination with 5 subsequently afforded 39, which was deprotected at C(1) and O(15). Yamaguchi macrolactonization of the seco-acid thereafter afforded a macrocycle that underwent O-desilylation and inversion at C(4) to give (+)-brefeldin A following deprotection

    Documents

    DOI

    Original languageEnglish
    Number of pages4
    Pages (from-to)4254-4257
    JournalOrganic Letters
    Journal publication date2016
    Issue number17
    Volume18
    Early online date19 Aug 2016
    DOIs
    Publication statusPublished - 2016

      Research areas

    • Brefeldin A, antitumour agent, [3+2]-cycloaddition, allenylsulfone, Mitsunobu inversion

    ID: 89304273