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Annulative Methods Enable a Total Synthesis of the Complex Meroterpene Berkeleyone A
70
Citations
27
References
2016
Year
Bioorganic ChemistryEngineeringBerkeleyone AOrganic ChemistryChemistryMedicinal ChemistryBiosynthesisNovel OrganocatalystsSynthetic PathwaysBiochemistryAnnulative Methods EnableTotal SynthesisSynthesis MethodNatural Product SynthesisEnantioselective SynthesisBiomolecular EngineeringComplex MeroterpenesNatural SciencesSynthetic Chemistry
Synthetic pathways to complex meroterpenes derived from 3,5-dimethylorsellinic acid (DMOA) and farnesyl pyrophosphate have not been reported despite heavy biosynthetic and medicinal interest. Herein we report the first total synthesis of berkeleyone A, a potential gateway compound to a plethora of fungal-derived meroterpenes, in 13 steps. In addition, we have further developed a novel annulation reaction for the synthesis of hydroxylated 1,3-cyclohexadiones in a single step.
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