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• W1900524431 abstract "Compounds with the 1-azabicyclo[4.3.0]nonan-2-one nucleus have been prepared with methyl and isobutyl groups at C-6. The synthetic sequence was: geminal acylation to produce a but-2-enylcyclopentane-1,3-dione derivative, treatment with O-mesitylenesulfonylhydroxylamine and then Beckmann rearrangement with BF3·Et2O and cyclization of the amidic nitrogen onto the terminal double bond. In addition, the results of exploratory reactions are presented." @default.
• W1900524431 created "2016-06-24" @default.
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• W1900524431 date "2001-12-18" @default.
• W1900524431 modified "2023-09-23" @default.
• W1900524431 title "Synthesis of 6-alkyl analogues of the 1-azabicyclo[4.3.0]nonan-2-one system by a strategy of geminal acylation and Beckmann rearrangement" @default.
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• W1900524431 doi "https://doi.org/10.1039/b108164k" @default.
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