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. |
Issue Date: | 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: | 0018-019X |
SCOPUS: | 2-s2.0-84879334997 |
Appears in Collections: | Faculty of Science, Kragujevac |
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