First synthesis and absolute configuration of (-)-pyriculariol, a phytotoxin isolated from rice blast fungus, Magnaporthe grisea. Use of microwave irradiation to control Stille coupling reaction products

Ayaka Sasaki, Koji Tanaka, Yuuki Sato, Shigefumi Kuwahara, Hiromasa Kiyota

    Research output: Contribution to journalArticlepeer-review

    11 Citations (Scopus)

    Abstract

    First total synthesis of (-)-pyriculariol, a phytotoxin isolated from rice blast fungus, Magnaporthe grisea, was achieved to determine the absolute configuration of the natural product to be 5′R,6′S. The key step was Stille coupling reaction using microwave irradiation from -78 °C to control the reaction.

    Original languageEnglish
    Pages (from-to)4637-4638
    Number of pages2
    JournalTetrahedron Letters
    Volume50
    Issue number32
    DOIs
    Publication statusPublished - 2009 Aug 12

    ASJC Scopus subject areas

    • Biochemistry
    • Drug Discovery
    • Organic Chemistry

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