Functionalized enantiomerically pure 3,4-dehydropyrrolidin-2-one and 1,2-dehydropyrrolizidin-3-one systems have been achieved by intramolecular nitrile oxide cycloaddition, starting from enamido-oximes, and by subsequent reduction of the obtained cycloadducts. Copyright (C) 1996 Published by Elsevier Science Ltd

Functionalized enantiomerically pure 3,4-dehydropyrrolidin-2-one and 1,2-dehydropyrrolizidin-3-one systems have been achieved by intramolecular nitrile oxide cycloaddition, starting from enamido-oximes, and by subsequent reduction of the obtained cycloadducts. Copyright (C) 1996 Published by Elsevier Science Ltd

Intramolecular nitrile oxide cycloaddition (INOC) of substituted amido-oximes

CHIACCHIO, Ugo;RESCIFINA, Antonio;
1996

Abstract

Functionalized enantiomerically pure 3,4-dehydropyrrolidin-2-one and 1,2-dehydropyrrolizidin-3-one systems have been achieved by intramolecular nitrile oxide cycloaddition, starting from enamido-oximes, and by subsequent reduction of the obtained cycloadducts. Copyright (C) 1996 Published by Elsevier Science Ltd
Functionalized enantiomerically pure 3,4-dehydropyrrolidin-2-one and 1,2-dehydropyrrolizidin-3-one systems have been achieved by intramolecular nitrile oxide cycloaddition, starting from enamido-oximes, and by subsequent reduction of the obtained cycloadducts. Copyright (C) 1996 Published by Elsevier Science Ltd
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.11769/12954
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