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Diastereoisomeric 4a,10a-dihydrofusarubins: true metabolites of Fusarium solani

From National Research Council Canada

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DOIResolve DOI: https://doi.org/10.1139/v78-260
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Affiliation
  1. National Research Council of Canada. Atlantic Regional Laboratory
FormatText, Article
Abstract
In alkaline cultures of Ftisarinm solani fusarubin is formed by nonenzymic oxidation of two previously unknown dihydrofusarubins, rel-(3R,4aR,10aR)- and rel-(3R,4aR, 10aS)-5,10-dioxo-3,4,4a,5,10,10a-hexahydro-7-methoxy-3-methyl-3,6,9-trihydroxy-1H-naphtho[2,3-c]pyran.
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PublisherNational Research Council of Canada
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  • Canadian Journal of Chemistry 56, no. 11 (June 1978): 1593–1594.
LanguageEnglish
Peer reviewedYes
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Record identifierc4901e71-baf0-4bb7-963b-0c1f2d484d62
Record created2023-10-04
Record modified2023-10-04
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