Synthetic studies on sialoglycoconjugates 81: Synthesis of positional isomers of sialyl lewis X epitope containing 1-deoxy-D-glucose in place of n-acetylglucosamine, and their inhibitory activity to selectin-mediated adhesion

Article abstract of DOI:10.1080/07328309608005435

Three sialyl-Le^X epitope analogs, which carry fucose and α-sialyl-(2→3)-galactose residues at O-2 and O-3, O-3 and O-2, and O-4 and O-6 positions of 1-deoxy-D-glucose backbone, respectively, have been synthesized. Glycosylation of 1,5-anhydro-4

Full text of DOI:10.1080/07328309608005435

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Journal of Carbohydrate Chemistry
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Synthetic Studies on
Sialoglycoconjugates 81: Synthesis of
Positional Isomers of Sialyl Lewis X
Epitope Containing 1-Deoxy-d Glucose in
Place of N-Acetylglucosamine, and Their
Inhibitory Activity to Selectin-Mediated
Adhesion
Masahiro Yoshida a , Takako Suzuki a , Hideharu Ishida a , Makoto Kiso
a & Akira Hasegawa a
a Department of Applied Bioorganic Chemistry , Gifu University ,
Gifu, 501-11, Japan
Published online: 22 Aug 2006.
To cite this article: Masahiro Yoshida , Takako Suzuki , Hideharu Ishida , Makoto Kiso & Akira
Hasegawa (1996) Synthetic Studies on Sialoglycoconjugates 81: Synthesis of Positional Isomers of Sialyl
Lewis X Epitope Containing 1-Deoxy-d Glucose in Place of N-Acetylglucosamine, and Their Inhibitory
Activity to Selectin-Mediated Adhesion, Journal of Carbohydrate Chemistry, 15:2, 147-162, DOI:
10.1080/07328309608005435
To link to this article: http://dx.doi.org/10.1080/07328309608005435
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