Proceedings of the National Academy of Sciences · 1996 · 166 citations · 20 references
Natural SciencesChemistryMedicinal ChemistryNatural Product BiosynthesisOrganic ChemistrySynthetic Medicinal ChemistryAlkaloid BiosynthesisHeterocyclic ChemistryOrganic SynthesisPlant Natural Product BiosynthesisRetrosynthetic AnalysisAlkaloid Skeleton FormationBiosynthetic Intermediates In Alkaloid PathwaysBiosynthetic Pathway ConstructionBiosynthetic Pathway DesignBiosynthetic Pathway ElucidationDiscoveryPlant Alkaloids
The Daphniphyllum alkaloids are a group of highly complex polycyclic alkaloids. Examination of the structures if several members of this family of natural products led to a hypothesis about their mode of biosynthesis (depicted in Scheme I). Based on this hypothetical biosynthetic pathway, a laboratory synthesis was designed that incorporated as a key transformation the novel one-pot transformation of dialdehyde 24 to pentacyclic unsaturated amine 25. This process turned out to be an exceptionally efficient way to construct the pentacyclic nucleus of the Daphniphyllum alkaloids. However, a purely fortuitous discovery, resulting from accidental use of methylamine rather than ammonia, led to a great improvement in the synthesis and suggests an even more attractive possible biosynthesis.
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K. C. Nicolaou, Zhen Yang, Jimei Liu et al. · Nature · 1994 · 1.1K citations
The total synthesis of vitamin B12
R. B. Woodward · Pure and Applied Chemistry · 1973 · 327 citations · Full text
Agriculture, Biochemistry, Nutrition +13