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 CDCl 3 solutions.
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