Synthesis of a tri- and tetrasaccharide fragment specific for the Shigella flexneri serotype 5a O-antigen. A reinvestigation

Article abstract of DOI:10.1080/07328309908544033

Stereocontrolled, stepwise synthesis of methyl α-L-rhamnopyranosyl-(1→2)-[α-D-glucopyranosyl-(1→3)]-α-L-rhamnopyranoside (A(E)B, 1) and methyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranosyl -(1→2)-[α-D-glucopyranosyl-(1 →3)]-α-L-rhamnopy

Full text of DOI:10.1080/07328309908544033

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Journal of Carbohydrate Chemistry
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Synthesis of a Tri- and
Tetrasaccharide Fragment Specific
for the Shigella flexneri Serotype 5a
O-Antigen. A Reinvestigation
Laurence A. Mulard & Joël Ughetto-Monfrin
a Unité de Chimie Organique, Département de Biochimie et
Génétique Moléculaire , Institut Pasteur , 28 rue du Dr. Roux,
75724 Paris, Cedex 15, France
b Unité de Chimie Organique, Département de Biochimie et
Génétique Moléculaire , Institut Pasteur , 28 rue du Dr. Roux,
75724 Paris, Cedex 15, France
Published online: 27 Feb 2008.
To cite this article: Laurence A. Mulard & Joël Ughetto-Monfrin (1999) Synthesis of
a Tri- and Tetrasaccharide Fragment Specific for the Shigella flexneri Serotype 5a O-
Antigen. A Reinvestigation, Journal of Carbohydrate Chemistry, 18:7, 721-753, DOI:
10.1080/07328309908544033
To link to this article: http://dx.doi.org/10.1080/07328309908544033
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