Electrochemical phenylselenoetherification as a key step in the synthesis of (±)-curcumene ether

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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.

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Stevanovic̈, D., Pejovic̈, A., Damljanovic̈, I. S., Vukic̈evic̈, M. D., Dobrikov, G., Dimitrov, V., … Vukic̈evic̈, R. D. (2013). Electrochemical phenylselenoetherification as a key step in the synthesis of (±)-curcumene ether. Helvetica Chimica Acta, 96(6), 1103–1110. https://doi.org/10.1002/hlca.201200610

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