| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5265066 | Tetrahedron Letters | 2013 | 5 Pages |
Abstract
The EF-ring of ciguatoxin 3C, a marine toxin from the dinoflagellate Gambierdiscus toxicus, was stereoselectively synthesized by iterative use of a cyclic ether formation process based on chirality-transferring Ireland-Claisen rearrangement and ring-closing olefin metathesis.
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Authors
Keisuke Nogoshi, Daisuke Domon, Kenshu Fujiwara, Natsumi Kawamura, Ryo Katoono, Hidetoshi Kawai, Takanori Suzuki,