Abstract
Total synthesis of the proposed structure of brevenal, a natural marine polycyclic ether product, has been accomplished. The synthesis features (i) convergent synthesis of the pentacyclic polyether skeleton using our developed Suzuki-Miyaura coupling strategy and (ii) construction of the multi-substituted dienal side chain by CuTC-mediated Stille reaction. Comparison of the NMR data of the synthetic compound with those reported for the natural product revealed that the proposed structure of brevenal needs to be revised.
Original language | English |
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Pages (from-to) | 9648-9650 |
Number of pages | 3 |
Journal | Journal of the American Chemical Society |
Volume | 128 |
Issue number | 30 |
DOIs | |
Publication status | Published - 2006 Aug 2 |