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]

Citation
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
Citations number
33
Categorie Soggetti
Chemistry Analytical
Journal title
Volume
648
Issue
1
Year of publication
1993
Pages
119 - 129
Database
ISI
SICI code
Abstract
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.