Homochiral functionalized pyrrolidinone and pyrrolizidinone systems have been achieved by stereoselective intramolecular oxime-olefin cycloaddition starting from homochiral amino acids, and by subsequent reduction of the obtained fused isoxazolidines. Copyright (C) 1996 Elsevier Science Ltd

Homochiral functionalized pyrrolidinone and pyrrolizidinone systems have been achieved by stereoselective intramolecular oxime-olefin cycloaddition starting from homochiral amino acids, and by subsequent reduction of the obtained fused isoxazolidines. Copyright (C) 1996 Elsevier Science Ltd

An asymmetric approach to pyrrolidinone and pyrrolizidinone systems by intramolecular oxime-olefin cycloaddition

CHIACCHIO, Ugo;PISTARA', Venerando;RESCIFINA, Antonio;
1996-01-01

Abstract

Homochiral functionalized pyrrolidinone and pyrrolizidinone systems have been achieved by stereoselective intramolecular oxime-olefin cycloaddition starting from homochiral amino acids, and by subsequent reduction of the obtained fused isoxazolidines. Copyright (C) 1996 Elsevier Science Ltd
1996
Homochiral functionalized pyrrolidinone and pyrrolizidinone systems have been achieved by stereoselective intramolecular oxime-olefin cycloaddition starting from homochiral amino acids, and by subsequent reduction of the obtained fused isoxazolidines. Copyright (C) 1996 Elsevier Science Ltd
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/13006
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