Abstract
A base-catalyzed condensation of phenyl acetate with acid chloride, followed by intramolecular cyclization and microwave-assisted cross-metathesis reaction, leads to the first total synthesis of psoralidin, a natural product with a broad range of biological activities, in a highly convergent and regioselective manner.
| Original language | English |
|---|---|
| Pages (from-to) | 2750-2754 |
| Number of pages | 5 |
| Journal | Journal of Organic Chemistry |
| Volume | 74 |
| Issue number | 7 |
| DOIs | |
| State | Published - Apr 3 2009 |
Funding
| Funders | Funder number |
|---|---|
| National Center for Complementary and Integrative Health | R01AT002890 |
ASJC Scopus subject areas
- Organic Chemistry