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  • A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene.

    Author(s)
    Banwell, MG
    Coster, MJ
    Karunaratne, OP
    Smith, JA
    Griffith University Author(s)
    Coster, Mark J.
    Year published
    2002
    Metadata
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    Abstract
    The enantiomerically pure cis-1,2-diol I, which is obtained by microbial oxidn. of naphthalene, has been converted, via a sequence of reactions including oxidative C-C bond cleavage, decarbonylation and ring-closing metathesis steps, into the natural product (+)-goniodiol (II).The enantiomerically pure cis-1,2-diol I, which is obtained by microbial oxidn. of naphthalene, has been converted, via a sequence of reactions including oxidative C-C bond cleavage, decarbonylation and ring-closing metathesis steps, into the natural product (+)-goniodiol (II).
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    Journal Title
    Journal of the Chemical Society, Perkin Transactions 1
    Volume
    2002
    DOI
    https://doi.org/10.1039/b205230j
    Subject
    Medicinal and biomolecular chemistry
    Organic chemistry
    Publication URI
    http://hdl.handle.net/10072/22670
    Collection
    • Journal articles

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