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• W2016065246 abstract "The synthesis of the marine natural products zonarone and isozonarone was achieved via (+)-albicanic acid, a sesquiterpene of the drimane type. Coupling of the appropiate drimane-synthon with lithiated hydroquinone ethers led to sesquiterpene arenes, which were further modified to the target molecules. Stereoselective epoxidation followed by regioselective opening of the oxirane ring yielded yahazunol." @default.
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• W2016065246 date "2002-05-01" @default.
• W2016065246 modified "2023-09-25" @default.
• W2016065246 title "Total synthesis of yahazunol, zonarone and isozonarone" @default.
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• W2016065246 doi "https://doi.org/10.1016/s0040-4020(02)00346-0" @default.
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