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Ring substituents of N-acetylglucosamine have little influence on the orientation of fucose and galactose. Also an exchange of N-acetylglucosamine in the sLe' tetrasaccharide for glucose preserves all relevant NOE contacts (e.g., Fuc-H5-Gal-H 2 = 250 pm).
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After preparation of this manuscript, a crystal structure of the Lewis X \ trisaccharide was published with a fucose-5H to galactose-2H distance of 264 pm. Thus the spatial structure of Fig. 4 is not only adopted in isotropic solution but also in the solid state
-
After preparation of this manuscript, a crystal structure of the Lewis X \ trisaccharide was published (F. Yvelin, Y. Zhang, J. Mallet, F. Robert. Y Jeannin, P. Shaȳ, Carbohydr. Lett. 1996, 1, 475-482), with a fucose-5H to galactose-2H distance of 264 pm. Thus the spatial structure of Fig. 4 is not only adopted in isotropic solution but also in the solid state.
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