Abstract
A strategy for the synthesis of 1-deoxynojirimycin (DNJ) derivatives from L-sorbose is described. The sequence involved eight steps and afforded DNJ derivatives in 13% to 44% overall yield.
| Original language | English |
|---|---|
| Pages (from-to) | 626-640 |
| Number of pages | 15 |
| Journal | Journal of Carbohydrate Chemistry |
| Volume | 30 |
| Issue number | 7-9 |
| DOIs | |
| Publication status | Published - 1 Sep 2011 |
Keywords
- 1-Deoxynojirimycin
- Lactol
- Wittig reactions