Skip to main navigation Skip to search Skip to main content

Chemoenzymatic total synthesis of the phytotoxic geranylcyclohexentriol (-)-phomentrioloxin

  • Xinghua Ma
  • , Martin G. Banwell*
  • , Anthony C. Willis
  • *Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    28 Citations (Scopus)

    Abstract

    The enantiomeric form, 1R, of the structure (1S) assigned to the phytotoxic natural product phomentrioloxin has been synthesized in seven steps from the homochiral cis-1,2-dihydrocatechol 3. These studies reveal that the true structure of phomentrioloxin is represented by 1R and not by 1S.

    Original languageEnglish
    Pages (from-to)1514-1518
    Number of pages5
    JournalJournal of Natural Products
    Volume76
    Issue number8
    DOIs
    Publication statusPublished - 23 Aug 2013

    Cite this