Total syntheses of bioactive natural products from carbohydrates

Kuniaki Tatsuta, Seijiro Hosokawa

    Research output: Contribution to journalArticle

    23 Citations (Scopus)

    Abstract

    Total syntheses of bioactive natural products recently accomplished in our laboratories are described. They are classified by structures of target molecules and are focused on our original approach to their own structures. The target molecules include nanaomycin, kalafungin, BE-54238B, tetracycline, rosmarinecine, thienamycin, luminacines C1 and C2, tetrodecamycin, cochleamycin A, and tubelactomicin A, which have been synthesized as optically pure form from carbohydrates.

    Original languageEnglish
    Pages (from-to)397-410
    Number of pages14
    JournalScience and Technology of Advanced Materials
    Volume7
    Issue number5
    DOIs
    Publication statusPublished - 2006 Jul

    Fingerprint

    Carbohydrates
    Biological Products
    Molecules
    Tetracycline
    BE 54238B
    tubelactomicin A
    tetrodecamycin
    kalafungin
    rosmarinecine
    thienamycin
    cochleamycin A

    Keywords

    • Carbohydrate
    • Enantiodivergent synthesis
    • Intramolecular Diels-Alder reaction
    • Michael-Dieckmann cyclization
    • Natural product
    • Structural determination
    • Total synthesis

    ASJC Scopus subject areas

    • Materials Science(all)

    Cite this

    Total syntheses of bioactive natural products from carbohydrates. / Tatsuta, Kuniaki; Hosokawa, Seijiro.

    In: Science and Technology of Advanced Materials, Vol. 7, No. 5, 07.2006, p. 397-410.

    Research output: Contribution to journalArticle

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