| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1345761 | Tetrahedron: Asymmetry | 2014 | 5 Pages |
A straightforward linear synthetic strategy has been developed for the synthesis of the pentasaccharide repeating unit of the cell wall O-antigenic polysaccharide of enteroadherent Escherichia coli O154 strain. Newly developed glycosylation conditions using glycosyl trichloroacetimidate derivatives as glycosyl donors and nitrosyl tetrafluoroborate as the glycosylation activator have been used in all of the glycosylation reactions throughout the synthetic scheme. The stereochemical outcomes of the glycosylations were excellent and the yields were very good.
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p-Methoxyphenyl (3-O-acetyl-2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranosideC42H45N3O11[α]D25=+49 (c 1.0, CHCl3).Source of chirality: l-rhamnose, d-galactosamine.
p-Methoxyphenyl (2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranosideC40H43N3O10[α]D25=+64 (c 1.0, CHCl3).Source of chirality: l-rhamnose, d-galactosamine.
p-Methoxyphenyl (3-O-acetyl-2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranosideC62H67N3O15[α]D25=+54 (c 1.0, CHCl3).Source of chirality: l-rhamnose, d-galactosamine.
p-Methoxyphenyl (2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α--rhamnopyranosyl)-(1→3)-2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranosideC60H65N3O14[α]D25=+55 (c 1.0, CHCl3).Source of chirality: l-rhamnose, d-galactosamine.
p-Methoxyphenyl (3-O-acetyl-2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranosideC82H89N3O19[α]D25=+71 (c 1.0, CHCl3).Source of chirality: l-rhamnose, d-galactosamine.
p-Methoxyphenyl (2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-l-rhamnopyranosyl)-(1→3)-2-azido-4,6-O-benzylidene-2-deoxy-α-d-galactopyranosideC80H87N3O18[α]D25=+115 (c 1.0, CHCl3).Source of chirality: l-rhamnose, d-galactosamine.
p-Methoxyphenyl (3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1→3)-(2,4-di-O-benzyl-α-L-rhamnopyranosyl)-(1→3)-2-azido-4,6-O-benzylidene-2-deoxy-α-D-galactopyranoside (11)C92H102N6O25[α]D25=+44 (c 1.0, CHCl3).Source of chirality: D-glucose, L-rhamnose, D-galactosamine.
p-Methoxyphenyl (2-acetamido-2-deoxy-α-D-mannopyranosyl)-(1→3)-(α-L-rhamnopyranosyl)-(1→3)-(α-L-rhamnopyranosyl)-(1→3)-(α-L-rhamnopyranosyl)-(1→3)-2-acetamido-2-deoxy-α-D-galactopyranoside (1)C41H64N2O24[α]D25=-130 (c 1.0, H2O).Source of chirality: D-glucose, L-rhamnose, D-galactosamine.
