Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10299
Title: Electrochemical phenylselenoetherification as a key step in the synthesis of (±)-curcumene ether
Authors: Stevanović, Dragana
Pejović, Anka
Damljanović, Ivan
Vukićević, Miomir
Dobrikov, Georgi
Dimitrov, Vladimir
Denić M.
Radulovic, Niko
Vukicevic R.
Journal: Helvetica Chimica Acta
Issue Date: 1-Jun-2013
Abstract: Two variants of a new pathway for the synthesis of (±)-curcumene ether are described. The key steps in these procedures are intramolecular cyclizations of 6-methyl-2-(4-methylphenyl)hept-6-en-2-ol and 2-methyl-6-(4-methylphenyl)hept-6-en-2-ol by means of an electrochemically generated phenylselenyl cation. This synthetic approach provides significantly better yields than the previously reported protocols. Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich.
URI: https://scidar.kg.ac.rs/handle/123456789/10299
Type: Article
DOI: 10.1002/hlca.201200610
ISSN: 0018019X
SCOPUS: 84879334997
Appears in Collections:Faculty of Science, Kragujevac
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