Abstract
A convergent synthesis of the F-K ring segment of brevetoxin B has been achieved via the intramolecular allylation of an α-chloroacetoxy ether and subsequent ring-closing metathesis.
| Original language | English |
|---|---|
| Pages (from-to) | 7929-7932 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 44 |
| Issue number | 43 |
| DOIs | |
| Publication status | Published - Oct 20 2003 |
| Externally published | Yes |
Keywords
- Brevetoxin B
- Convergent synthesis
- Polycyclic ethers
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
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Cite this
Kadota, I., Nishina, N., Nishii, H., Kikuchi, S., & Yamamoto, Y. (2003). Convergent synthesis of the F-K ring segment of brevetoxin B. Tetrahedron Letters, 44(43), 7929-7932. https://doi.org/10.1016/j.tetlet.2003.09.003