Copper-catalyzed 1,3-Dipolar Cycloaddition of Substituted N-Propargylindoles and Terminal Diazidoalkanes
- Authors: Sokolov V.B.1, Aksinenko A.Y.1, Goreva T.V.1, Epishina T.A.1, Samsonova A.N.1
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Affiliations:
- Institute of Physiologically Active Compounds
- Issue: Vol 88, No 6 (2018)
- Pages: 1266-1269
- Section: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/222277
- DOI: https://doi.org/10.1134/S1070363218060361
- ID: 222277
Cite item
Abstract
Copper-catalyzed alkyne-azide 1,3-dipolar cycloaddition was studied of substituted N-propargylindoles and diazidoalkanes leading to symmetric conjugates of substituted indoles with bistriazole-containing spacer.
About the authors
V. B. Sokolov
Institute of Physiologically Active Compounds
Author for correspondence.
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
A. Yu. Aksinenko
Institute of Physiologically Active Compounds
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
T. V. Goreva
Institute of Physiologically Active Compounds
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
T. A. Epishina
Institute of Physiologically Active Compounds
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432
A. N. Samsonova
Institute of Physiologically Active Compounds
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi proezd 1, Chernogolovka, 142432