Аннотация:
1,2-Epoxyperfluorocyclohexane reacts with 3,3’,4,4’-tetraaminobiphenyl (1 : 1 mol / mol) to give 4-(6,6,7,7,8,8,9,9-octafluoro- 6,7,8,9-tetrahydrophenazin-2-yl)benzene-1,2-diamine whose structure was determined by X-ray crystallography. Reactions of the latter with 1,2-epoxyperfluorocyclohexane or benzil bring about new fluorinated phenazine derivatives.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
T. I. Filyakova, V. I. Filyakova, A. Ya. Zapevalov, M. I. Kodess, P. A. Slepukhin, V. I. Saloutin, V. N. Charushin, “New derivatives of fluorine-containing phenazines”, Mendeleev Commun., 27:3 (2017), 290–292
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc1972
https://www.mathnet.ru/rus/mendc/v27/i3/p290
Эта публикация цитируется в следующих 5 статьяx:
N. S. Boltacheva, T. I. Filyakova, M. I. Kodess, M. A. Ezhikova, P. A. Slepukhin, V. I. Filyakova, V. I. Saloutin, V. N. Charushin, “3-(Trifluoromethyl)-1,2,3-propanetrione 2-oximes in the synthesis of new heterocyclic systems”, Russ Chem Bull, 72:3 (2023), 706
Marc Zeplichal, Joshua Gies, Johannes Bernd, Dilan Kancious Winslaws, Tieyan Chang, Yu-Sheng Chen, Steven H. Strauss, Olga V. Boltalina, Andreas Terfort, “Fluorinated Azaacenes: Efficient Syntheses, Structures, and Electrochemical Properties”, Journal of Fluorine Chemistry, 257-258 (2022), 109960
Jason C. Cole, Robin Taylor, “Intermolecular Interactions of Organic Fluorine Seen in Perspective”, Crystal Growth & Design, 22:2 (2022), 1352
Yu‐Xin Che, Xiao‐Ni Qi, Wen‐Juan Qu, Bing‐Bing Shi, Qi Lin, Hong Yao, You‐Ming Zhang, Tai‐Bao Wei, “Synthetic strategies of phenazine derivatives: A review”, Journal of Heterocyclic Chem, 59:6 (2022), 969
T. I. Filyakova, V. I. Filyakova, A. Ya. Zapevalov, M. I. Kodess, P. A. Slepukhin, V. I. Saloutin, V. N. Charushin, “3,4-Epoxyperfluorooxolane in the synthesis of new fluorine-containing furo[3,4-b]quinoxaline derivatives”, Mendeleev Commun., 28:5 (2018), 511–512
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