Отправить статью по E-mail Conjugation of Phenothiazine and Substituted Indoles via Copper-Catalyzed 1,3-Dipolar Cycloaddition
- Авторы: Sokolov V.1, Aksinenko A.1, Goreva T.1, Epishina T.1
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Учреждения:
- Institute of Physiologically Active Substances of the Russian Academy of Sciences
- Выпуск: Том 88, № 7 (2018)
- Страницы: 1546-1549
- Раздел: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/222343
- DOI: https://doi.org/10.1134/S1070363218070319
- ID: 222343
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Аннотация
Copper-catalyzed alkyne-azide 1,3-dipolar cycloaddition of substituted N-azidoalkylindoles and N-propargylphenothiazine led to the formation of conjugates of substituted indoles and phenothiazine combined with 1,2,3-triazole-containing alkylene spacers.
Об авторах
V. Sokolov
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Автор, ответственный за переписку.
Email: alaks@ipac.ac.ru
Россия, Severnyi proezd 1, Chernogolovka, 142432
A. Aksinenko
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Email: alaks@ipac.ac.ru
Россия, Severnyi proezd 1, Chernogolovka, 142432
T. Goreva
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Email: alaks@ipac.ac.ru
Россия, Severnyi proezd 1, Chernogolovka, 142432
T. Epishina
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Email: alaks@ipac.ac.ru
Россия, Severnyi proezd 1, Chernogolovka, 142432
