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

Anastasiya E Tarakanova 1
Anastasiya E Tarakanova
Maxim Aleksandrovich Zherebtsov 1
Maxim Aleksandrovich Zherebtsov
Maxim Vyacheslavovich Arsenyev 1, 2
Maxim Vyacheslavovich Arsenyev
Eugeny Vladimirovich Baranov 1
Eugeny Vladimirovich Baranov
Sergey Arturovich Chesnokov 1
Sergey Arturovich Chesnokov
Vladimir Kuzmich Cherkasov 1, 2
Vladimir Kuzmich Cherkasov
Published 2022-07-01
CommunicationVolume 32, Issue 4, 540-542
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Tarakanova A. E. et al. New tri-tert-alkyl substituted o-quinones of tetraline family // Mendeleev Communications. 2022. Vol. 32. No. 4. pp. 540-542.
GOST all authors (up to 50) Copy
Tarakanova A. E., Zherebtsov M. A., Arsenyev M. V., Baranov E. V., Chesnokov S. A., Cherkasov V. K. New tri-tert-alkyl substituted o-quinones of tetraline family // Mendeleev Communications. 2022. Vol. 32. No. 4. pp. 540-542.
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TY - JOUR
DO - 10.1016/j.mencom.2022.07.035
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.07.035
TI - New tri-tert-alkyl substituted o-quinones of tetraline family
T2 - Mendeleev Communications
AU - Tarakanova, Anastasiya E
AU - Zherebtsov, Maxim Aleksandrovich
AU - Arsenyev, Maxim Vyacheslavovich
AU - Baranov, Eugeny Vladimirovich
AU - Chesnokov, Sergey Arturovich
AU - Cherkasov, Vladimir Kuzmich
PY - 2022
DA - 2022/07/01
PB - Mendeleev Communications
SP - 540-542
IS - 4
VL - 32
ER -
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@article{2022_Tarakanova,
author = {Anastasiya E Tarakanova and Maxim Aleksandrovich Zherebtsov and Maxim Vyacheslavovich Arsenyev and Eugeny Vladimirovich Baranov and Sergey Arturovich Chesnokov and Vladimir Kuzmich Cherkasov},
title = {New tri-tert-alkyl substituted o-quinones of tetraline family},
journal = {Mendeleev Communications},
year = {2022},
volume = {32},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.07.035},
number = {4},
pages = {540--542},
doi = {10.1016/j.mencom.2022.07.035}
}
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Tarakanova, Anastasiya E., et al. “New tri-tert-alkyl substituted o-quinones of tetraline family.” Mendeleev Communications, vol. 32, no. 4, Jul. 2022, pp. 540-542. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2022.07.035.

Keywords

o-quinones
alkylation
electrochemistry
oxidation
phenol
selenium dioxide
tetralines
X-ray study

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.

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