Abstract
A racemic total synthesis of the sesquiterpenoid unit of the hybrid marine natural product polymaxenolide has been achieved based on a three-component assembly followed by ring-closing metathesis as the key steps. However, the spectral data of our product synthesized from Δ 9(15)-africanene by epoxidation were not identical with those of the natural product named epoxyafricanane. The structure confirmation of the synthetic nominal epoxyafricanane is described.
| Original language | English |
|---|---|
| Pages (from-to) | 6258-6263 |
| Number of pages | 6 |
| Journal | Journal of Organic Chemistry |
| Volume | 76 |
| Issue number | 15 |
| DOIs | |
| Publication status | Published - 2011 Aug 5 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 14 Life Below Water
ASJC Scopus subject areas
- Organic Chemistry
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