Abstract
More than 20,000 people suffer annually from ciguatera seafood poisoning in subtropical and tropical regions. The extremely low content of the causative neurotoxins, designated as ciguatoxins, in fish has hampered the isolation, detailed biological studies, and preparation of anti-ciguatoxin antibodies for detecting these toxins. The large (3 nanometers long) and complicated molecular structure of ciguatoxins has impeded chemists from completing their total synthesis. Our highly convergent strategic approach featuring the chemoselective ring-closing metathesis reaction as a key tactic has enabled the total synthesis of ciguatoxin CTX3C, which will provide a practical supply for further studies.
| Original language | English |
|---|---|
| Pages (from-to) | 1904-1907 |
| Number of pages | 4 |
| Journal | Science |
| Volume | 294 |
| Issue number | 5548 |
| DOIs | |
| Publication status | Published - Nov 30 2001 |
| Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General
Fingerprint
Dive into the research topics of 'Total synthesis of ciguatoxin CTX3C'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS