1421257-50-2Relevant articles and documents
An Ireland-Claisen rearrangement/RCM based approach for the construction of the EF-ring of ciguatoxin 3C
Nogoshi, Keisuke,Domon, Daisuke,Fujiwara, Kenshu,Kawamura, Natsumi,Katoono, Ryo,Kawai, Hidetoshi,Suzuki, Takanori
, p. 676 - 680 (2013)
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.