METHODS FOR THE DETERMINATION OF THE ENANTIOMERIC PURITY OF THE C3-SYNTHONS GLYCIDOL (2,3-EPOXY-1-PROPANOL) AND SOLKETAL [2,2-DIMETYL-4-(HYDROXYMETHYL)-1,3-DIOXOLANE]
A. Geerlof et al., METHODS FOR THE DETERMINATION OF THE ENANTIOMERIC PURITY OF THE C3-SYNTHONS GLYCIDOL (2,3-EPOXY-1-PROPANOL) AND SOLKETAL [2,2-DIMETYL-4-(HYDROXYMETHYL)-1,3-DIOXOLANE], Journal of chromatography, 648(1), 1993, pp. 119-129
Accurate and reliable methods are presented for the determination of e
nantiomeric excess values of glycidol (2,3-epoxy-1-propanol), glycidyl
esters, solketal [2,2-dimethyl-4-(hydroxymethyl)-1,3-dioxolane], homo
logous 1,3-dioxolane alcohols and substituted primary propanols in bio
logical samples. One method consists of derivatization of the samples
with 2,3,4,6-tetra-O-acetyl-beta-glucopyranosyl isothiocyanate, follow
ed by separation of the resulting diastereomers on a non-chiral revers
ed-phase (C18) HPLC column. The second method uses direct injection of
(aqueous) samples on to capillary GC columns coated with chiral stati
onary phases (2,3,6-tri-0-methyl-beta- or a 2,3,6-tri-0-trifluoroacety
l-gamma-cyclodextrin). The advantages and disadvantages of both method
s are discussed.