Аннотация:
Chlorination of 2-aryl-1-hydroxyindole-5,6-dicarbonitriles with N-chlorosuccinimide affords previously unknown 3,3-dichloro-3H-indole 1-oxides instead of the expected 1-hydroxy- 3-chloroindoles. The latter can be prepared in good yields by treatment of the above 3,3-dichloro-3H-indole 1-oxides with piperidine in ethanol.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
Zh. V. Chirkova, M. V. Kabanova, S. I. Filimonov, I. G. Abramov, A. V. Samet, G. A. Stashina, “The C-3 chlorination of 2-aryl-1-hydroxyindoles”, Mendeleev Commun., 27:5 (2017), 498–499
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2040
https://www.mathnet.ru/rus/mendc/v27/i5/p498
Эта публикация цитируется в следующих 4 статьяx:
M. R. Crampton, Organic Reaction Mechanisms Series, Organic Reaction Mechanisms · 2017, 2020, 213
Zhanna V. Chirkova, Mariya V. Kabanova, Sergey I. Filimonov, Igor G. Abramov, Anél Petzer, Rialette Hitge, Jacobus P. Petzer, Kyrill Yu. Suponitsky, “Optimization of pyrrolo[3,4‐f]indole‐5,7‐dione and indole‐5,6‐dicarbonitrile derivatives as inhibitors of monoamine oxidase”, Drug Development Research, 80:7 (2019), 970
Zh. V. Chirkova, M. V. Kabanova, S. I. Filimonov, A. V. Samet, G. A. Stashina, T. N. Sudzilovskaya, “Chlorination of 2-substituted 1-hydroxyindoles”, Russ Chem Bull, 67:6 (2018), 1083
D. V. Vorobyeva, T. P. Vasilyeva, S. N. Osipov, “Trifluoromethylated 5-aminoderivatives of (indol-3-yl)acetic acid”, Russ Chem Bull, 67:8 (2018), 1459
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