Homochiral functionalized pyrrolidine and pyrrolizidine systems have been achieved by stereoselective intramolecular 1,3-dipolar cycloaddition of homochiral nitrones, starting from homochiral amino acids, and by subsequent reduction of the obtained cycloadducts.
Homochiral functionalized pyrrolidine and pyrrolizidine systems have been achieved by stereoselective intramolecular 1,3-dipolar cycloaddition of homochiral nitrones, starting from homochiral amino acids, and by subsequent reduction of the obtained cycloadducts.
ALPHA-AMINO-ACIDS AS CHIRAL EDUCTS FOR STEREOSELECTIVE SYNTHESES OF PYRROLIDINE AND PYRROLIZIDINE SYSTEMS
CHIACCHIO, Ugo;RESCIFINA, Antonio;
1995-01-01
Abstract
Homochiral functionalized pyrrolidine and pyrrolizidine systems have been achieved by stereoselective intramolecular 1,3-dipolar cycloaddition of homochiral nitrones, starting from homochiral amino acids, and by subsequent reduction of the obtained cycloadducts.File in questo prodotto:
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