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