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  • Total Synthesis of (+)-Angelmarin

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    Author(s)
    Magolan, Jakob
    Coster, Mark J
    Griffith University Author(s)
    Coster, Mark J.
    Magolan, Jakob
    Year published
    2009
    Metadata
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    Abstract
    An efficient 8-step enantioselective total synthesis of (+)-angelmarin, starting from commercially available umbelliferone, has been achieved. Key reactions include olefin cross-metathesis and a Shi epoxidation-cyclization sequence.An efficient 8-step enantioselective total synthesis of (+)-angelmarin, starting from commercially available umbelliferone, has been achieved. Key reactions include olefin cross-metathesis and a Shi epoxidation-cyclization sequence.
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    Journal Title
    Journal of Organic Chemistry
    Volume
    74
    Issue
    14
    DOI
    https://doi.org/10.1021/jo900613u
    Copyright Statement
    This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Organic Chemistry, copyright 2009 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://dx.doi.org/10.1021/jo900613u.
    Subject
    Medicinal and biomolecular chemistry
    Organic chemistry
    Organic chemical synthesis
    Publication URI
    http://hdl.handle.net/10072/30553
    Collection
    • Journal articles

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