Organic Letters · 2009 · 78 citations · 22 references
PharmacyChemistryMedicinal ChemistryOrganic ChemistryPlant BiochemistrySynthetic Medicinal ChemistryAlkaloid BiosynthesisAromatic PlantsHeterocyclic ChemistryMedicinal PlantsAlkaloid Skeleton FormationIndole AlkaloidsPhytochemical CompositionPlant AlkaloidsQuinoline AlkaloidsX-ray Diffraction Analysis
A phytochemical study on Melodinus henryi has led to the isolation of two novel alkaloids, melohenines A (1), a monoterpenoid indole alkaloid with additional skeletal carbons arranged compactly in eight rings, and melohenine B (2), an alkaloid with an unprecedented 6/9/6/6 tetracyclic ring system regarded as a key intermediate from indole to quinoline alkaloids. Their structures were elucidated by means of spectroscopic methods and further confirmed by X-ray diffraction analysis.
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Unique Monoterpenoid Indole Alkaloids from <i>Alstonia scholaris</i>
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