中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | 2'-(benzyloxycarbonyl)benzyl 4,6-O-benzylidene-α-D-mannopyranoside | 365535-43-9 | C28H28O8 | 492.526 |
—— | 2'-(benzyloxycarbonyl)benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside | —— | C35H34O8 | 582.65 |
—— | 2'-carboxybenzyl 2,3,4,6-tetra-O-benzyl-α-D-mannopyranoside | 220662-68-0 | C42H42O8 | 674.791 |
—— | 2'-(benzyloxycarbonyl)benzyl 3,4-di-O-benzyl-2-O-pivaloyl-α-D-mannopyranoside | 365534-75-4 | C40H44O9 | 668.784 |
—— | 2-(hydroxycarbonyl)benzyl 2,3-di-O-benzyl-4,6-O-cyclohexylidene-α-D-mannopyranoside | 365534-65-2 | C34H38O8 | 574.671 |
—— | 2'-carboxybenzyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside | 365534-63-0 | C35H34O8 | 582.65 |
—— | 2-(hydroxycarbonyl)benzyl 4,6-O-benzoyl-2,3-O-cyclohexylidene-α-D-mannopyranoside | 365534-66-3 | C34H34O10 | 602.638 |
—— | 2'-carboxybenzyl 3-O-benzyl-4,6-O-benzylidene-2-O-p-methoxybenzyl-α-D-mannopyranoside | —— | C36H36O9 | 612.676 |
—— | 2'-carboxybenzyl 3-O-benzyl-4,6-O-benzylidene-2-O-levulinyl-α-D-mannopyranoside | —— | C33H34O10 | 590.627 |
—— | methyl 2,3,6-tri-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl α-D-mannopyranosyl) α-D-glucopyranoside | —— | C62H66O11 | 987.199 |
—— | 2'-(allyloxycarbonyl)benzyl (3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl)-(1->3)-4,6-O-benzylidene-2-azido-2-deoxy-α-D-glucopyranoside | —— | C44H45N3O12 | 807.854 |
—— | 2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl-(1->3)-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose | —— | C46H54O11 | 782.928 |
—— | 2'-(allyloxycarbonyl)benzyl (3-O-benzyl-4,6-O-benzylidene-2-O-p-methoxybenzyl-β-D-mannopyranosyl)-(1->3)-4,6-O-benzylidene-2-azido-2-deoxy-α-D-glucopyranoside | —— | C52H53N3O13 | 928.005 |
—— | 2'-(allyloxycarbonyl)benzyl (3-O-benzyl-4,6-O-benzylidene-2-O-levulinyl-α-D-mannonopyranosyl)-(1->2)-(3-O-benzyl-4,6-O-benzylidene-β-D-mannopyranosyl)-(1->3)-4,6-O-benzylidene-2-azido-2-deoxy-α-D-glucopyranoside | —— | C69H71N3O19 | 1246.33 |
The synthesis of the suitably protected form (1) of the tetrasaccharide repeat unit, →2)-α-D-Manp-(1→2)-β-D-Manp-(1→3)-α-D-GlcpNAc-(1→6)-α-D-Manp-(1→ (A), of the O-antigen polysaccharide of the lipopolysaccharide from Escherichia coli O77 has been accomplished by latentactive glycosylation employing the 2′-carboxybenzyl (CB) gly coside method. In addition to previously used latent glycosyl donors, 2′-(benzyloxycarbonyl)benzyl (BCB) glycosides, new latent glycosyl donors, 2'-(allyloxycarbonyl)benzyl (ACB) glycosides, have been introduced as a direct precursor for the active CB glycosides. We also demonstrate that 4,6-O-benzylidene-2-azido-2-deoxy-α-D-mannopyranoside (7) has been readily prepared from D-glucosamine in good yield.Key words: Escherichia coli O77, glycosylation, 2′-carboxybenzyl (CB) glycosides, 2′-(allyloxycarbonyl)benzyl (ACB) glycosides, glycosyl donor.