Journal of the Chemical Society Chemical Communications · 1984 · 97 citations · 0 references
PharmacyBiochemistryBioisosterismBioorganic ChemistryStructural BiologyMutagenicity AssessmentMycotoxin-producing FungiMycotoxinsChemical Mutagen SafetyMutagenesis In FungiNuclear Overhauser Effect SpectroscopyRelative Configuration DeterminationStructure Elucidation Of Fungal MetabolitesSubstitution Pattern Analysis
The assignment of structure (1) to fusarin C, a mutagen isolated from cultures of Fusarium moniliforme is based on a detailed study of its high-field 1H and 13C n.m.r. spectra and X-ray crystallography of the 8Z isomer of (1) which defined the substitution pattern and relative configuration of the 2-pyrrolidone moiety; nuclear Overhauser enhancement experiments indicate that the 2E,4E,6E,8E,10E polyene chromophore of (1) exists in solution as an equilibrium between two conformers with s-cis and s-trans topology of the C-5–C-6 single bond.