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Cyclopentanones reactions with organoaluminum reagents

Another synthetic route via the Beckmann rearrangement, which is promoted by organoaluminum reagent along with alkylation, involves a new stereoselective reduction of the imino group. The starting oxime sulfonate (228) was synthesized from cyclopentanone (226) in three steps Reaction of 226 with 1-undecene in the presence of silver oxide produced the a-undecylcyclopentanone (227) which on successive treatment with hydroxylamine and methanesulfonyl chlo-ride-triethylamine gave the mesylate (228). Treatment of the oxime mesylate... [Pg.242]


See other pages where Cyclopentanones reactions with organoaluminum reagents is mentioned: [Pg.233]   


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Organoaluminum reactions

Organoaluminum reagents

Reactions with organoaluminum reagents

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