Facile synthesis of the cyclohexane fragment of enacloxins, a series of antibiotics isolated from Frateuria sp. W-315

Aki Saito, Wataru Igarashi, Hiroyuki Furukawa, Teiko Yamada, Shigefumi Kuwahara, Hiromasa Kiyota

    Research output: Contribution to journalArticlepeer-review

    2 Citations (Scopus)

    Abstract

    An efficient and good yield synthesis of the cyclohexane moiety of enacyloxins, a series of antibiotics isolated from Frateuria sp. W-315, was achieved from D-quinic acid using a successive Barton - McCombie deoxygenation.

    Original languageEnglish
    Pages (from-to)766-769
    Number of pages4
    JournalBioscience, Biotechnology and Biochemistry
    Volume78
    Issue number5
    DOIs
    Publication statusPublished - 2014

    Keywords

    • Antibiotics
    • Barton-McCombie deoxygenation
    • D-quinic acid
    • Enacyloxin

    ASJC Scopus subject areas

    • Biotechnology
    • Analytical Chemistry
    • Biochemistry
    • Applied Microbiology and Biotechnology
    • Molecular Biology
    • Organic Chemistry

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