Abstract
(Formula Represented) The first total synthesis of gambierol, a marine polycyclic ether toxin, has been achieved. The synthesis features the Pd(PPh3)4/CuCl/LiCl-promoted Stille coupling for the stereoselective construction of the sensitive triene side chain that includes a conjugated (Z,Z)-diene moiety. † The University of Tokyo and CREST, JST. ‡ Tohoku University.
Original language | English |
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Pages (from-to) | 2981-2984 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 4 |
Issue number | 17 |
DOIs | |
Publication status | Published - 2002 Aug 22 |