Publication | Closed Access
A Formal Synthesis of Antimalarial Diterpenoid 7,20-Diisocyanoadociane
22
Citations
11
References
2011
Year
Medicinal ChemistryPharmaceutical ChemistryCorey ’Diversity Oriented SynthesisDerivative (Chemistry)Natural SciencesDiversity-oriented SynthesisOrganic ChemistryChemistryPharmacologyAntimalarial Diterpenoid 7,20-DiisocyanoadocianeSynthetic ChemistrySynthetic Intermediate 2Natural Product Synthesis
Abstract A formal synthesis of antimalarial diterpenoid 7,20-diisocyanoadociane, isolated from marine sponge Adocia sp., was achieved. The authors synthesized Corey’s synthetic intermediate 2 for 7,20-diisocyanoadociane. This synthesis involves the synthesis of a perhydropyrene derivative using a sequential isomerization–intramolecular Diels–Alder reaction as the key step.
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