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Pyrroloiminoquinone Alkaloids: Discorhabdins and Makaluvamines
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2005
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PharmacotherapyPharmaceutical ChemistryMolecular PharmacologyMedicinal ChemistryDiversity Oriented SynthesisPyrroloiminoquinone AlkaloidsBiochemistryPyrroloiminoquinone Alkaloid FamilyDiversity-oriented SynthesisTotal SynthesisPharmacologyNatural Product SynthesisNatural SciencesHerbal MedicineDrug DiscoveryHerb-drug InteractionMedicineSynthetic ChemistryUnique Highly-fused Structures
The pyrroloiminoquinone alkaloid family consisting of discorhabdins and makaluvamines exhibits antitumor activities derived from their unique highly-fused structures. The total synthesis of them and the key reactions used in the total synthesis of these compounds are described. Keywords: discorhabdin c, yamamura's synthesis, heathcock's synthesis, white's formal synthesis, makaluvamine a, kraus's synthesis