Abstract
Synthesis of three tetrasaccharides, namely, 0-α-L-fucopyranosyl-(l—»3)-0-(2-acetamido-2-deoxy-P-D-glucopyranosyl)-(l-*3)-0-(β-D-galactopyranosyl)- (1 ->4)-β-D-glucopyranose (7), 0-α-L-fucopyranosyl-(l ->4)-0-(2-acetamido-2-deoxy-P-D-glucopyranosyl)-(1^3)-0-(β-D-galactopyranosyl)-(l-44)-D- glucopyranose (9), and 0-α-L-fucopyranosyl-(l—»3)-0-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(l->6)-0(β-D-galactopyranosyl)-(l-44)-D-glucopyranose (15) has been described. Their structures have been established by 13C NMR spectroscopy.
| Original language | English |
|---|---|
| Pages (from-to) | 269-278 |
| Number of pages | 10 |
| Journal | Journal of Carbohydrate Chemistry |
| Volume | 10 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 1 1991 |
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Dive into the research topics of 'Synthesis of two isomeric tetrasaccharides 0-α-l-fucopyranosyl-(1—>3) and (l->4)-0-(2-acetamido-2-deoxy-β-d-glucopyranosyl)-(l—>3)-0-(p-d-galactopyranosyl)-(l—»4)-d- glucopyranose and a related tetrasaccharide o-α-l-fucopyranosyl-(l->3)-0-(2-acetamido-2-deoxy-β-d- glucopyranosyl-(l—>6)-0-(β-d-galactopyranosyl)-(l—>4)-d-glucopyranose1'. Together they form a unique fingerprint.Cite this
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