Title of article :
Convergent synthesis of the ABCDE-ring fragment of the Caribbean ciguatoxin C-CTX-1
Author/Authors :
Inoue، نويسنده , , Masayuki and Saito، نويسنده , , Fumihito and Iwatsu، نويسنده , , Masafumi and Ishihara، نويسنده , , Yuuki and Hirama، نويسنده , , Masahiro، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Abstract :
Ciguatoxin C-CTX-1 was isolated as a principal causative toxin of ciguatera seafood poisoning in the Caribbean Sea, and is structurally classified as a ladder-shaped polycyclic ether. In this Letter, we report the convergent synthesis of the pentacyclic left half of C-CTX-1, based on a newly developed acyl radical strategy.
Keywords :
radicals , Enol ethers , S-acetals , Ciguatoxins , polyethers , O
Journal title :
Tetrahedron Letters
Journal title :
Tetrahedron Letters
