## Abstract The photosensitized oxygenation of the β,γ‐unsaturated ketonic sesquiterpene, davanone, is described. Treatment of davanone epoxide with an acid ion exchange resin yields a stereoisomeric mixture of the davana ethers, sesquiterpenoids containing two reduced furan rings.
✦ LIBER ✦
Terpenoids Derived from Linalyl Oxide. Part 2. The isolation and synthesis of nordavanone, A C11-terpenoid from Artemisia pallens
✍ Scribed by Alan F. Thomas; Michel Ozainne
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- German
- Weight
- 242 KB
- Volume
- 57
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The isolation, absolute stereochemistry, and synthesis of a new C~11~‐terpenoid, 3__S__,4__S__,7__R__‐3,7‐dimethyl‐4,7‐oxido‐non‐8‐en‐2‐one, related to davanone, are described.
📜 SIMILAR VOLUMES
Terpenoids Derived from Linalyl Oxide, P
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Alan F. Thomas; Renée Dubini
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Terpenoids Derived from Linalyl Oxide. P
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Alan F. Thomas
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## Abstract Based on spectra, the structure of the title compound has been attributed to a new sesquiterpenoid isolated from __Artemisia Pallens__. From the same fraction of the oil, the conjugated unsaturated ketone, isodavanone (**2**), was identified.