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A novel radical induced rearrangement of the caryophyllene skeleton

✍ 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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✦ 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 -_


πŸ“œ SIMILAR VOLUMES


A novel rearrangement of the latifolin s
✍ Darshan Kumari; S.K. Mukerjee; T.R. Seshadri πŸ“‚ Article πŸ“… 1967 πŸ› Elsevier Science 🌐 French βš– 191 KB

## 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.

Novel rearrangement during dehydration.
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## 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.