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.File in questo prodotto:
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