Abstract:
New tri-tert-alkyl substituted o-quinones of 3-tert-alkyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-1,2-dione chemotype were obtained from phenol and 2,5-dichloro-2,5-dimethylhexane, with the SeO2 oxidation of the sterically hindered phenol moiety having been performed at the final step. The electrochemical reduction of these quinones proceeds in two stages: the first reduction wave (E1/2 = –0.60 ÷ –0.62 V) is reversible, while the second stage is irreversible.
Citation:
A. E. Tarakanova, M. A. Zherebtsov, M. V. Arsenyev, E. V. Baranov, S. A. Chesnokov, V. K. Cherkasov, “New tri-tert-alkyl substituted o-quinones of tetraline family”, Mendeleev Commun., 32:4 (2022), 540–542
Linking options:
https://www.mathnet.ru/eng/mendc719
https://www.mathnet.ru/eng/mendc/v32/i4/p540
This publication is cited in the following 3 articles: