Chirality · 2007 · 54 citations · 18 references
Life SciencesBotanyPlant SciencesMicrobial EcologyMycologyPlant BiochemistryFungal BiochemistryFungal Natural Product BiosynthesisFungal Secondary MetabolitesStructural ElucidationAbsolute Configuration AssignmentAbsolute Configuration DeterminationDiffraction AnalysisEndophytic Fungal MetabolitesEndophytic FungiSecondary MetabolitesSpectroscopic CharacterizationX-ray Diffraction Analysis
Three new massarilactones E-G (1-3) and the massarilactone acetonide (4) were isolated from the ethyl acetate extract of the endophytic fungus Coniothyrium sp., associated with the plant Artimisia maritima. Their structures were determined by analysis of the 1D and 2D NMR and mass spectroscopic data. The structure of massarilactones E (1) was confirmed by X-ray diffraction analysis, and its absolute configuration determined by the solid-state CD/TDDFT method.
18
On enantiomorph-polarity estimation
H. D. Flack · Acta Crystallographica Section A Foundations of Crystallography · 1983 · 10.4K citations
Natural Sciences, Chemistry, Physics +10
Mark E. Casida, Christine Jamorski, Kim C. Casida et al. · The Journal of Chemical Physics · 1998 · 5K citations
Endophytic fungi: a source of novel biologically active secondary metabolites
Barbara Schulz, Christine Boyle, Siegfried Draeger et al. · Mycological Research · 2002 · 1.2K citations
Life Sciences, Botany, Microbiology +14