Abstract
Chemical investigations of the Australian plant Eremophila mitchellii resulted in the isolation of the novel tetracyclic sesquiterpene lactones mitchellenes A-C (1-3), the new sesquiterpene acids mitchellenes D and E (4 and 5), and the previously reported natural products 14-hydroxy-6,12-muuroloadien- 15-oic acid (6), casticin, and centaureidin. The chemical structures of all compounds were determined by extensive 1D/2D NMR and MS data analysis. Mitchellenes A-C are the first tetracyclic sesquiterpene lactones to be reported; a biosynthetic pathway is proposed for these unique secondary metabolites.
| Original language | English |
|---|---|
| Pages (from-to) | 1888-1893 |
| Number of pages | 6 |
| Journal | Journal of Natural Products |
| Volume | 74 |
| Issue number | 9 |
| DOIs | |
| Publication status | Published - 23 Sept 2011 |
| Externally published | Yes |
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