ENANTIOSELECTIVE SEPARATIONS BY CAPILLARY GC ON DERIVATIZED CYCLODEXTRINS .1. SEPARATION OF SOME RACEMIC 2,2-DIALKYL-4-ALKOXYCARBONYL-1,3-DIOXOLANE DERIVATIVES ON PERMETHYLATED ALPHA-CYCLODEXTRIN, BETA-CYCLODEXTRIN AND GAMMA-CYCLODEXTRIN
K. Jaques et al., ENANTIOSELECTIVE SEPARATIONS BY CAPILLARY GC ON DERIVATIZED CYCLODEXTRINS .1. SEPARATION OF SOME RACEMIC 2,2-DIALKYL-4-ALKOXYCARBONYL-1,3-DIOXOLANE DERIVATIVES ON PERMETHYLATED ALPHA-CYCLODEXTRIN, BETA-CYCLODEXTRIN AND GAMMA-CYCLODEXTRIN, HRC. Journal of high resolution chromatography, 16(12), 1993, pp. 703-707
The enantioseparation of some 2,2-dialkyl-4-alkoxycarbonyl-1,3-di-oxol
ane derivatives, which are important intermediates in the total synthe
sis of a number of biologically active compounds, was studied by means
of capillary gas chromatography (CGC). The chromatographic results, o
btained on columns coated with permethylated alpha-, beta- and gamma-c
yclodextrin respectively, are reported. Out of sixteen compounds, thir
teen could be separated with a resolution superior to 1,2. One racemat
e could not be separated on any of the columns. Considerations concern
ing the separation mechanism are proposed.