Abstract
The chemical synthesis of disaccharides 1 and 2, useful building-blocks for the preparation of a new series of heparin related oligosaccharides containing the unusual sequence (GlcN-IdoA)(n), is described. In addition, the orthogonality of the protective groups would allow access to a wide array of differently sulfated oligosaccharides. As the simplest members of this new class of oligomer, the synthesis of sulfated disaccharides 3 and 4 fully deprotected is reported.
| Original language | English |
|---|---|
| Pages (from-to) | 9867-9880 |
| Number of pages | 14 |
| Journal | Tetrahedron |
| Volume | 55 |
| Publication status | Published - 1999 |
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