Dimeric sesquiterpene lactone. Structure of isoabsinthin acid isomerization of absinthin derivatives
โ Scribed by J. Beauhaire; J.L. Fourrey; J.Y. Lallemand; M. Vullhorgne
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 200 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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๐ SIMILAR VOLUMES
The structure and stereochemistry of mexicanin F, a novel dimeric nor-sesquiterpene lactone isolated from He&n&m mexicanum, have been stablish\_ ed from spectral and single-crystal X-ray analyses. Several years ago, one of us reported the physical constants of the mexicanins A, B,..., H which, in ad
In a recent comunication, Risinqer, Green and Green' have suggested that the iodo-lactone obtained2 frcm the action of iodine and potassium iodide in alkaline solutior. on norborn-S-ene-2-endo-carboxylic acid should be formulated aa 6-exo-iodo-S-endo-hydroxynorbornane-2-endo-carboxylic acid leotone