Computational and NMR investigations of diastereoisomeric aggregates arising from the interaction of 9-O-[(S)- or (R)-1-(1- naphthyl)ethylcarbamate]dihydroquinine and the two enantiomers of N-(3,5-dinitrobenzoyl)alanine methyl ester pointed out the origin of chiral discrimination phenomena occurring in CDCl3 solutions.

Chiral discrimination processes by C9 carbamate derivatives of dihydroquinine: interaction mechanisms of diastereoisomeric 9-O-[(S)- or (R)-1-(1-naphthyl)ethylcarbamate]dihydroquinine and the two enantiomers of N-(3,5-dinitrobenzoyl)alanine methyl ester

UCCELLO BARRETTA, GLORIA;BALZANO, FEDERICA;
2008-01-01

Abstract

Computational and NMR investigations of diastereoisomeric aggregates arising from the interaction of 9-O-[(S)- or (R)-1-(1- naphthyl)ethylcarbamate]dihydroquinine and the two enantiomers of N-(3,5-dinitrobenzoyl)alanine methyl ester pointed out the origin of chiral discrimination phenomena occurring in CDCl3 solutions.
2008
UCCELLO BARRETTA, Gloria; Balzano, Federica; Bardoni, S.; Vanni, L.; Giurato, L.; Guccione, G.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/122609
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