Asteriscanolide. A sesquiterpene lactone with a new natural skeleton.
β Scribed by A. San Feliciano; A.F. Barrero; M. Medarde; J.M. Miguel del Corral; A. Aramburu; A. Perales; J. Fayos
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 310 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A sesquiterpene lactone was isolated from the hexane extract of Asteriscus aquaticus. Its constitution and stereochemistry were determined by spectroscopic techniques, principaZly two-dimensional NMR correlations (COSY, HCCORR,RELAYl and with the interpretation of certain chemical transformations. The results were confirmed by X-ray diffraction and the name asteriscane is proposed for the new natural skeleton.
By repeated chromatography of a methanol defatted hexane extract of Asteriscus aquaticus L.
(familly: Compositae) it was possible to isolate a small amount of a crystalline compound (m.p.
π SIMILAR VOLUMES
## Abstract Porosadienone (1), a sesquiterpene ketone with the new 8(7β8)β__abeo__βeudesmane skeleton, was isolated from the commercial Brazilian __Phoebe__ oil (__Phoebe porosa__ Mez. syn. __Oreodaphne porosa__ Mez.). The structure was established by ^1^Hβ and ^13^CβNMR data and by reduction to th