Abstract
The formal divergent synthesis of natural products (−)-warburganal and synthesis of (+)-isodrimenin has been developed from α-hydroxy β,γ-unsaturated aldehyde I, which was easily prepared from available (+)-sclareolide in 5 steps. Reduction of intermediate I to II via an aldehyde reduction provides a 10-step access to (−)-warburganal, while oxidation of I to III via allylic oxidation and in situ hemiacetalization facilitates a 9-step synthesis of (+)-isodrimenin.
| Original language | English |
|---|---|
| Pages (from-to) | 2573-2577 |
| Number of pages | 5 |
| Journal | Natural Product Research |
| Volume | 40 |
| Issue number | 9 |
| DOIs | |
| State | Published - 2026 |
| Externally published | Yes |
Keywords
- Natural product
- divergent synthesis
- isodrimenin
- warburganal
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