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• W1992163721 abstract "The Beckmann rearrangement of the syn and anti isomers of the spirocyclic oxime derived from a 16β,23:23,26-diepoxy-5β-cholestan-22-one was studied. Whereas the anti isomer always follows the Beckmann fragmentation course, the syn isomer, depending on the reaction conditions, follows the normal Beckmann rearrangement course and/or the isomerization to the anti isomer followed by the fragmentation course." @default.
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• W1992163721 date "2009-01-01" @default.
• W1992163721 modified "2023-10-18" @default.
• W1992163721 title "Beckmann reactions of steroidal spirocyclic oximes derived from the 16β,23:23,26-diepoxy-22-oxo moiety" @default.
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• W1992163721 doi "https://doi.org/10.1016/j.steroids.2008.09.013" @default.
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