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 |
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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