Issue 16, 1985

Analysis of the absolute configuration of chiral [16O, 17O, 18O]sulphate monoesters by Fourier transform infrared spectroscopy

Abstract

The symmetric and antisymmetric [double bond splayed left]SO2 stretching region of the i.r. spectrum provides a means of distinguishing between (1R)-3-hydroxy-1-methylpropyl [(S)-16O,17O,18O]sulphate and [(R)-16O,17O,18O]sulphate after cyclisation to an isotopomeric mixture of (4R)-4-methyl-2,2-dioxo-1,3,2-dioxanthianes.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1075-1078

Analysis of the absolute configuration of chiral [16O, 17O, 18O]sulphate monoesters by Fourier transform infrared spectroscopy

G. Lowe and M. J. Parratt, J. Chem. Soc., Chem. Commun., 1985, 1075 DOI: 10.1039/C39850001075

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