Electrochemical Phenylselenoetherification as a Key Step in the Synthesis of (±)-Curcumene Ether
✍ Scribed by Stevanović, Dragana; Pejović, Anka; Damljanović, Ivan S.; Vukićević, Mirjana D.; Dobrikov, Georgi; Dimitrov, Vladimir; Denić, Marija S.; Radulović, Niko S.; Vukićević, Rastko D.
- Book ID
- 120473218
- Publisher
- John Wiley and Sons
- Year
- 2013
- Tongue
- German
- Weight
- 202 KB
- Volume
- 96
- Category
- Article
- ISSN
- 0018-019X
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📜 SIMILAR VOLUMES
lldione. whichhas been produced efficiently by means of electrochemical method. Pentalenene belongs to a group of triquinane sesquiterpenesl and is attractive to synthetic chemists.2f We describe herein a synthesis of (f)-pentalenene u&g electrochemical method as a key step. The known phenol (1) (4
1l-dione as a key intermediate has been produced efficiently by means of electrochemical methods.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
A highly oxygenated isocedrene, which has been isolated from Acourtia Nana, has been synthesized as a racemate via its dial precursor. The key step is the construction of a tricyclo [5.3.1.01,5]undec-9-ene-8,11-dione by means of electrochemical oxidation of the corresponding phenol.