Abstract
The chemical composition of the marine sponge Phorbas tenacior was investigated in depth. The anchinopeptolides A–D bearing a central pyrrolidinone were isolated together with a new congener named anchinopeptolide E corresponding to an epimer of anchinopeptolide C. The relative configuration of the central core of anchinopeptolide E was determined by extensive NMR analyses. Additionally, the previously isolated cyclobutane derivative cycloanchinopeptolide C was not detected from the sponge extract but could be synthesised by a photoinduced intramolecular [2+2] cycloaddition giving convincing evidence for its artefactual origin.
| Original language | English |
|---|---|
| Pages (from-to) | 5515-5518 |
| Number of pages | 4 |
| Journal | European Journal of Organic Chemistry |
| Volume | 2019 |
| Issue number | 31-32 |
| DOIs | |
| Publication status | Published - 1 Sep 2019 |
Keywords
- Anchinopeptolide
- Cycloaddition
- Modified peptides
- Natural products
- Phorbas tenacior
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