A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting from beta-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused delta-lactams. Copyright (C) 1996 Published by Elsevier Science Ltd
A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting from beta-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused delta-lactams. Copyright (C) 1996 Published by Elsevier Science Ltd
Intramolecular nitrone cycloaddition: Stereoselective synthesis of piperidine systems
CHIACCHIO, Ugo;RESCIFINA, Antonio;
1996-01-01
Abstract
A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting from beta-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused delta-lactams. Copyright (C) 1996 Published by Elsevier Science LtdFile in questo prodotto:
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