X-RAY AND NMR-STUDIES ON THE ROTATIONAL-ISOMERISM ABOUT THE C(5)-C(6)BOND OF 6-SUBSTITUTED METHYL 2,3,4,-TRI-O-ACETYL-6-X-ALPHA-D-GLUCOPYRANOSIDE DERIVATIVES
D. Mentzafos et al., X-RAY AND NMR-STUDIES ON THE ROTATIONAL-ISOMERISM ABOUT THE C(5)-C(6)BOND OF 6-SUBSTITUTED METHYL 2,3,4,-TRI-O-ACETYL-6-X-ALPHA-D-GLUCOPYRANOSIDE DERIVATIVES, Journal of chemical crystallography, 25(4), 1995, pp. 157-164
The rotamers about the C(5)-C(6) bond of a series of 2,3,4-tri-O-acety
l-6-X-alpha-D-glucopyranozide derivatives resulting by substitution at
C(6) or O(6) have been studied with H-1-NMR spectroscopy (400 MHz) an
d X-ray structure analysis. The methyl cetyl-6-O-triphenyl-methyl-alph
a-D-glucopyranoside and the yl-2,3,4-tri-O-acetyl-alpha-D-glucopyranos
e-6-yl)- pyridinium nitrate crystallize in the P2(1) space group with
a = 14.940(1), b = 11.232(1), c = 9.0773(7), and beta = 94.480(7) and
a = 7.670(1), b = 15.384(3), c = 9.624(1) and beta = 104.90(1), respec
tively; the methyl 3,4-tri-O-acetyl-6-O-nitro-alpha-D-glucopyranoside
and methyl O-acetyl-6-O-deoxy-6-iodo-alpha-D-glucopyrano-side crystall
ize in the P2(1)2(1)2(1) space group with a = 5.630(1), b = 14.360(1)
and c = 22.388(3), and a = 5.556(1), b = 14.303(6) and c = 21.963(6),
respectively.