Organic Letters · 2007 · 46 citations · 10 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryBiomimetic SynthesisEnzyme InhibitionHeterocyclic ChemistryHeterocyclic CompoundsMarine Drug DiscoveryOrganic SynthesisBioactive HeterocyclesBioactive Marine MetabolitesMarine Sponge MetabolitesMarine Sponge Natural Product BiosynthesisMarine-derived Enzyme InhibitorsNatural Product Total SynthesisTotal Synthesis-derived AnaloguesZinc Enzymes
[reaction: see text] A convergent second generation total synthesis of the heterocyclic marine sponge metabolite ageladine A has been achieved by using a biomimetically inspired 6pi-2-azatriene electrocyclization as the key step for formation of the imidazolopyridine moiety.
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Copper-Catalyzed Coupling of Amides and Carbamates with Vinyl Halides
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A stereoselective synthesis of (Z)-1-iodo-1-alkenes
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