Email this article Catalytic alkylation of substituted indoles with (phenothiazin-10-yl)propene-1-ones
- Authors: Sokolov V.B.1, Aksinenko A.Y.1, Epishina T.A.1, Goreva T.V.1
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Affiliations:
- Institute of Physiologically Active Compounds
- Issue: Vol 86, No 5 (2016)
- Pages: 1028-1031
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/214913
- DOI: https://doi.org/10.1134/S1070363216050078
- ID: 214913
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Abstract
Alkylation of substituted indoles (carbazoles, tetrahydrocarbazoles, and gamma-carbolines) with (phenothiazinyl)propenones catalyzed by cesium fluoride has led to the formation of 1-(phenothiazin-10-yl)-3-(carbazol-9-yl)propane-1-ones, (1-phenothiazin-10-yl)-3-(tetrahydrocarbazol-9-yl)propane-1-ones, and 3-(tetrahydropyrido[4,3-b]indol-5-yl)-1-(phenothiazin-10-yl)propane-1-ones, respectively.
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About the authors
V. B. Sokolov
Institute of Physiologically Active Compounds
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi pr. 1, Chernogolovka, 142432
A. Yu. Aksinenko
Institute of Physiologically Active Compounds
Author for correspondence.
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi pr. 1, Chernogolovka, 142432
T. A. Epishina
Institute of Physiologically Active Compounds
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi pr. 1, Chernogolovka, 142432
T. V. Goreva
Institute of Physiologically Active Compounds
Email: alaks@ipac.ac.ru
Russian Federation, Severnyi pr. 1, Chernogolovka, 142432
