CP-225,917 and CP-263,114 synthesis support studies: Testing a radical cyclization strategy for installation of the side-chains

Martin G. Banwell, Mark J. Coster, Alison J. Edwards, Markus Vögtle

    Research output: Contribution to journalArticlepeer-review

    6 Citations (Scopus)

    Abstract

    The selenocarbonate (18) has been prepared and shown to react with hexabutyldistannane hydride/allyltributylstannane to give, via a radical cyclization/allylation sequence, the lactone (21) embodying vicinal and trans-related functionality likely to be appropriate for elaboration to the side-chains associated with the title compounds (1) and (2) (phomoidrides A and B).

    Original languageEnglish
    Pages (from-to)577-583
    Number of pages7
    JournalAustralian Journal of Chemistry
    Volume56
    Issue number6
    DOIs
    Publication statusPublished - 2003

    Fingerprint

    Dive into the research topics of 'CP-225,917 and CP-263,114 synthesis support studies: Testing a radical cyclization strategy for installation of the side-chains'. Together they form a unique fingerprint.

    Cite this