Abstract
The total synthesis of (-)-frondosin B, the enantiomer of naturally-occuring (+)-frondosin B, is described, wherein a palladium-catalyzed cyclization is used to establish the tetracyclic ring system of the natural product. Graphical Abstract.
Original language | English (US) |
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Pages (from-to) | 9675-9686 |
Number of pages | 12 |
Journal | Tetrahedron |
Volume | 60 |
Issue number | 43 SPEC. ISS. |
DOIs | |
State | Published - Oct 18 2004 |
Keywords
- Frondosin
- Heck reaction
- Palladium catalysis
- Total synthesis
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry