Abstract
A practical and efficient total synthesis of (±)-galanthamine was achieved from commercially available materials through a novel approach, in which the construction of its core structure and the special allylic group were based on a successive semipinacol rearrangement/desilyation/cyclization and Saegusa-Ito oxidation, respectively.
| Original language | English |
|---|---|
| Pages (from-to) | 1823-1825 |
| Number of pages | 3 |
| Journal | Organic Letters |
| Volume | 8 |
| Issue number | 9 |
| DOIs | |
| State | Published - 27 Apr 2006 |
| Externally published | Yes |