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• W2026792323 abstract "Abnormal Beckmann fragmentation of Hajos ketone oxime regioselectively forms of a chiral 1-oxygenated 2,2-dimethyl-4-methylene-cyclohexan skeleton. Using this transformation as a key step, the total synthesis of (−)-elegansidiol, an oxygenated mono-carbocyclic sesquiterpenoid, was achieved." @default.
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• W2026792323 date "2007-06-01" @default.
• W2026792323 modified "2023-10-03" @default.
• W2026792323 title "Total synthesis of (−)-elegansidiol by using an abnormal Beckmann fragmentation of Hajos ketone oxime as a key step" @default.
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• W2026792323 doi "https://doi.org/10.1016/j.tet.2007.03.123" @default.
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