Synthesis of the enantiomer of the structure assigned to the natural product nobilisitine A

Brett D. Schwartz, Matthew T. Jones, Martin G. Banwell, Ian A. Cade

    Research output: Contribution to journalArticlepeer-review

    33 Citations (Scopus)

    Abstract

    The synthesis of the enantiomer of the structure, 1, assigned to the natural product nobilisitine A has been accomplished using the enantiomerically pure cis-1,2-dihydrocatechol 4 as starting material. The 1H and 13C NMR spectral data derived from compound ent-1 do not match those reported for the natural product, thus suggesting its structure has been incorrectly assigned.

    Original languageEnglish
    Pages (from-to)5210-5213
    Number of pages4
    JournalOrganic Letters
    Volume12
    Issue number22
    DOIs
    Publication statusPublished - 19 Nov 2010

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