A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting from β-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused δ-lactams.
Intramolecular nitrone cycloaddition. Stereoselective synthesis of piperidine systems.
PIPERNO, Anna;ROMEO, Roberto
1996-01-01
Abstract
A synthetic approach to isomerically functionalized piperidine systems has been designed by intramolecular nitrone cycloaddition, starting from β-enamidoaldehydes, and by subsequent reductive ring-opening of the obtained fused δ-lactams.File in questo prodotto:
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