Issue 1, 1973

Configurational correlations for chiral epoxides by nuclear magnetic resonance spectroscopy in optically active solvents

Abstract

The use of optically active 2,2,2-trifluorophenylethanol as an n.m.r. solvent causes enantiomeric spectral dissimilarities for chiral epoxides; the relative field positions of non-equivalent n.m.r. resonance are related to the absolute configuration of the solvated epoxides.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 25-26

Configurational correlations for chiral epoxides by nuclear magnetic resonance spectroscopy in optically active solvents

I. Moretti, F. Taddei, G. Torre and N. Spassky, J. Chem. Soc., Chem. Commun., 1973, 25 DOI: 10.1039/C39730000025

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