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 Ltd
1996
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
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/10617
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