Blockwise approach to fragments of the O-specific polysaccharide of Shigella flexneri serotype 2a: convergent Synthesis of a decasaccharide representative of a dimer of the branched repeating unit.
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Glycotherapy: new advances inspire a reemergence of glycans in medicineStructures of synthetic O-antigen fragments from serotype 2a Shigella flexneri in complex with a protective monoclonal antibodyAntibody recognition of carbohydrate epitopes†.Stereoselective glycosylation of glucosamine: the role of the N-protecting group.Linear synthesis of the branched pentasaccharide repeats of O-antigens from Shigella flexneri 1a and 1b demonstrating the major steric hindrance associated with type-specific glucosylation.Preparation of synthetic glycoconjugates as potential vaccines against Shigella flexneri serotype 2a disease.Synthesis of two linear PADRE conjugates bearing a deca- or pentadecasaccharide B epitope as potential synthetic vaccines against Shigella flexneri serotype 2a infection.CGTase-catalysed cis-glucosylation of L-rhamnosides for the preparation of Shigella flexneri 2a and 3a haptens.
P2860
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P2860
Blockwise approach to fragments of the O-specific polysaccharide of Shigella flexneri serotype 2a: convergent Synthesis of a decasaccharide representative of a dimer of the branched repeating unit.
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2004 nî lūn-bûn
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Blockwise approach to fragment ...... f the branched repeating unit.
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Blockwise approach to fragment ...... f the branched repeating unit.
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type
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Blockwise approach to fragment ...... f the branched repeating unit.
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Blockwise approach to fragment ...... f the branched repeating unit.
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Blockwise approach to fragment ...... f the branched repeating unit.
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Blockwise approach to fragment ...... f the branched repeating unit.
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P2093
P356
P1476
Blockwise approach to fragment ...... f the branched repeating unit.
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P2093
Armelle Phalipon
Corina Costachel
Frédéric Bélot
Karen Wright
Laurence A Mulard
P304
P356
10.1021/JO035125B
P407
P577
2004-02-01T00:00:00Z