Abstract
A synthesis of the amino sugar 2-amino-2,3-didesoxyribose is described. Starting from D-glucosamine, ß-methylfuranoside was obtained in eight steps in 20% yield. This carbohydrate is a novel building block for nucleosides and for backbone modified antisense oligonucleotides with 2'-5' amide linkages.
| Original language | English |
|---|---|
| Pages (from-to) | 109-116 |
| Number of pages | 8 |
| Journal | Monatshefte für Chemie |
| Volume | 135 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 2004 |
Austrian Fields of Science 2012
- 301207 Pharmaceutical chemistry
- 104015 Organic chemistry
- 304003 Genetic engineering
Keywords
- Amino sugar
- Carbohydrates
- Oligonucleotides
- Ribose derivatives
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