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- Publisher
- Wiley
- Copyright
- Copyright © 2001 Wiley Subscription Services
- ISSN
- 1433-7851
- eISSN
- 1521-3773
- DOI
- 10.1002/1521-3773(20010316)40:6<1090::AID-ANIE10900>3.0.CO;2-W
- Publisher site
- See Article on Publisher Site
Abstract
Access to polycyclic polyethers is facilitated by a synthetic strategy involving two‐step B‐alkyl Suzuki coupling reactions for the stereoselective construction of the polyether skeleton. Thus, a convergent synthetic route to the heptacyclic GHIJKLM ring system 1 of ciguatoxin, a marine algal toxin implicated in ciguatera fish poisoning, was developed. Bn=benzyl.
Journal
Angewandte Chemie International Edition – Wiley
Published: Jan 16, 2001
Keywords: ; ; ; ;