Email this article Conjugation of Phenothiazine and Substituted Indoles via Copper-Catalyzed 1,3-Dipolar Cycloaddition
- Authors: Sokolov V.B.1, Aksinenko A.Y.1, Goreva T.V.1, Epishina T.A.1
-
Affiliations:
- Institute of Physiologically Active Substances of the Russian Academy of Sciences
- Issue: Vol 88, No 7 (2018)
- Pages: 1546-1549
- Section: Letters to the Editor
- URL: https://journal-vniispk.ru/1070-3632/article/view/222343
- DOI: https://doi.org/10.1134/S1070363218070319
- ID: 222343
Cite item
Open Access
Access granted
Subscription Access
Abstract
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.
About the authors
V. B. Sokolov
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Author for correspondence.
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
A. Yu. Aksinenko
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
T. V. Goreva
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
T. A. Epishina
Institute of Physiologically Active Substances of the Russian Academy of Sciences
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
Supplementary files
