A novel radical induced rearrangement of the caryophyllene skeleton
β Scribed by L.M. van der Linde; A.J.A. van der Weerdt
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 188 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The addition of an acetyl radical on caryophyllene leads to formation of the four isomeric ketones 5-8 involving a novel rearrangement of the caryophyllene skeleton.
The acid catalyzed rearrangement of caryophyllene 1 has been studied in detail'. The final re-_ action products are clovene 2, caryolan-l-01 3 and neoclovene 4 -_
π SIMILAR VOLUMES
## Latifolin (Id) Is an important memter of the neoflavanoia group of -pwa6. AS recently descriteal its synthesis Involves an ionic coupling of trlmethoxy benzene tc,) and o-methoxy clnnamyl ceticn CC9>, the latter being generated from o-methoxp clnnamyl chloride by a Lewis acid.
## Abstract On treatment with phosphorus oxychloride, the decalin derivative 6 underwent rearrangement yielding principally the perhydroazulene derivative 8. Similar rearrangement was also observed on dehydration of the decalin derivative 9.
Laboratorio per la Chimica delle molecole di interesse biologic0 de1 C.N.N.