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J Nat Prod ; 74(3): 357-64, 2011 Mar 25.
Article in English | MEDLINE | ID: mdl-21250701

ABSTRACT

Ciguatoxins, the principal causative toxins of ciguatera seafood poisoning, are large ladder-like polycyclic ethers. We report a highly stereoselective 6-exo radical cyclization/ring-closing olefin metathesis sequence to construct the syn/trans-fused polyether system. The new method was applied to the practical synthesis of ciguatoxin CTX3C.


Subject(s)
Ciguatera Poisoning/etiology , Ciguatoxins/chemistry , Ciguatoxins/chemical synthesis , Seafood/poisoning , Sulfoxides/chemistry , Vinyl Compounds/chemistry , Ciguatoxins/pharmacology , Cyclization , Models, Molecular , Molecular Structure , Stereoisomerism , Structure-Activity Relationship
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