期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 73, 期 21, 页码 8635-8638出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo801564c
关键词
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Biosynthetic studies on spiro-mamakone A (1), a potently cytotoxic and antimicrobial Compound from an endophytic fungus isolated from the New Zealand native tree Knightia excelsa (rewarewa), confirm the polyketide origins of this unique compound belonging to the spirobisnaphthalene class of compounds. The biosynthesis proceeds via an unprecedented symmetric enedione with the two halves of the Molecule being formed from two separate pentaketide units connected by oxidative coupling
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