PREPARATION AND CRYSTAL AND MOLECULAR-STRUCTURE OF 6-O-[(2S)-2,3-EPOXYPROPYL]-1,2 3,4-DI-O-ISOPROPYLIDENE-ALPHA-D-GALACTOPYRANOSE - PYRANOID RING CONFORMATION IN 1,2/3,4-DI-O-ISOPROPYLIDENE-GALACTOPYRANOSE ANDRELATED SYSTEMS/
P. Koll et al., PREPARATION AND CRYSTAL AND MOLECULAR-STRUCTURE OF 6-O-[(2S)-2,3-EPOXYPROPYL]-1,2 3,4-DI-O-ISOPROPYLIDENE-ALPHA-D-GALACTOPYRANOSE - PYRANOID RING CONFORMATION IN 1,2/3,4-DI-O-ISOPROPYLIDENE-GALACTOPYRANOSE ANDRELATED SYSTEMS/, Carbohydrate research, 265(2), 1994, pp. 237-248
The title compound was isolated by several recrystallisations from a 1
:1 mixture of diastereomers which was obtained in 75% yield from the r
eaction of ,2:3,4-di-O-isopropylidene-alpha-D-galactopyranose with epi
chlorohydrin. The absolute configuration of this isomer (30% yield) wa
s established by X-ray crystallography. The conformation of the pyrano
id ring in this compound is compared to those in related situations. I
n all these cases the pyranoid ring adopts a heavily distorted conform
ation which is described on average as between the screw-boat S-O(5) a
nd the twist-boat (''skew''-boat) T-O(2) with deviations in the direct
ion of the boat B-2,B-5 in most cases. The puckering parameters for al
l such reported pyranoid rings were calculated or recalculated, and ar
e given within expanded conventions of carbohydrate nomenclature.