Research output: Contribution to journal › Article › peer-review
Journal | Organic Letters |
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Date | Published - 17 Jan 2008 |
Issue number | 2 |
Volume | 10 |
Number of pages | 4 |
Pages (from-to) | 353-356 |
Original language | English |
The first synthetic route to the tricyclic core of the dictyosphaeric acids has been established starting from readily available (S)-(-)-4-(tert-butyldimethylsilyloxy)cyclohexenone and involving 9 steps, including a ring-closing metathesis to produce a 13-membered macrolactone, and a doubly tethered intramolecular Michael addition.
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