Enantiomerically pure isoxazolidine-fused delta-lactams have been obtained by intramolecular nitrone cycloaddition starting from homochiral amido aldehydes. The stereocenter of the homochiral precursor controls the stereochemical course of the process.

Enantiomerically pure isoxazolidine-fused delta-lactams have been obtained by intramolecular nitrone cycloaddition starting from homochiral amido aldehydes. The stereocenter of the homochiral precursor controls the stereochemical course of the process.

Stereoselective synthesis of enantiomerically pure isoxazolidine-fused delta-lactams

CHIACCHIO, Ugo;RESCIFINA, Antonio;
1999-01-01

Abstract

Enantiomerically pure isoxazolidine-fused delta-lactams have been obtained by intramolecular nitrone cycloaddition starting from homochiral amido aldehydes. The stereocenter of the homochiral precursor controls the stereochemical course of the process.
1999
Enantiomerically pure isoxazolidine-fused delta-lactams have been obtained by intramolecular nitrone cycloaddition starting from homochiral amido aldehydes. The stereocenter of the homochiral precursor controls the stereochemical course of the process.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11769/34139
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