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Mendeleev Communications, 2022, Volume 32, Issue 4, Pages 540–542
DOI: https://doi.org/10.1016/j.mencom.2022.07.035
(Mi mendc719)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

New tri-tert-alkyl substituted o-quinones of tetraline family

A. E. Tarakanovaa, M. A. Zherebtsova, M. V. Arsenyevab, E. V. Baranova, S. A. Chesnokova, V. K. Cherkasovab

a G.A. Razuvaev Institute of Organometallic Chemistry, Russian Academy of Sciences, Nizhnii Novgorod, Russian Federation
b N.I. Lobachevsky State University of Nizhni Novgorod, Nizhni Novgorod, Russian Federation
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.
Keywords: o-quinones, phenol, tetralines, alkylation, oxidation, selenium dioxide, X-ray study, electrochemistry.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (575.2 Kb)


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
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  • https://www.mathnet.ru/eng/mendc/v32/i4/p540
  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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