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Ketene Acetal and Spiroacetal Constituents of the Marine Fungus <i>Aigialus </i><i>p</i><i>arvus</i> BCC 5311
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References
2004
Year
BiologyFungal DiversityBiosynthesisAntifungal AgentBiochemistryBioassay-guided IsolationNatural SciencesMedicineSpectral AnalysisSecondary MetaboliteUnique CompoundsMicrobiologyPharmacologySpiroacetal ConstituentsRelative StereochemistryKetene Acetal
Aigialone (1) and aigialospirol (2), two structurally unique compounds, were isolated from the mangrove fungus Aigialus parvus BCC 5311. The structure of the new ketene acetal 1 was elucidated by spectral analysis, and its relative stereochemistry was determined by X-ray crystallography. The stereochemistry of aigialospirol (2), elucidated by NMR spectral analysis, suggested that this compound is possibly derived from hypothemycin (3), a metabolite previously isolated from this same fungus.
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