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Structure elucidation of the fumonisins, mycotoxins from Fusarium moniliforme
Journal of the Chemical Society Chemical Communications · 1988 · pp. 743–743
S. Catherine Bezuidenhout✉Wentzel C.A. GelderblomCharles P. Gorst‐AllmanR. Marthinus HorakWalter F. O. MarasasGerhard SpitellerRobert Vleggaar
Abstract
The structures of the fumonisins, a family of structurally related mycotoxins isolated from cultures of Fusarium moniliforme, were elucidated by mass spectrometry and 1H and 13C n.m.r. spectroscopy as the diester of propane-1,2,3-tricarboxylic acid and either 2-acetylamino- or 2-amino-12,16-dimethyl-3,5,10,14,15-pentahydroxyicosane as well as in each case the C-10 deoxy analogue; in all cases both the C-14 and C-15 hydroxy groups are involved in ester formation with the terminal carboxy group of propane-1,2,3-tricarboxylic acid.
Mycotoxins in Agriculture and FoodSynthesis and Biological EvaluationMicrobial Natural Products and BiosynthesisFusariumMycotoxinTricarboxylic acidChemistryMass spectrometryStereochemistryPropaneOrganic chemistryCitric acid cycleBiochemistry
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Mycotoxins and their effects on human and animal health
Food Control · 2013 · 545 citations
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