Conjugation of Phenothiazine and Substituted Indoles via Copper-Catalyzed 1,3-Dipolar Cycloaddition


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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.

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V. Sokolov

Institute of Physiologically Active Substances of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: alaks@ipac.ac.ru
俄罗斯联邦, Severnyi proezd 1, Chernogolovka, 142432

A. Aksinenko

Institute of Physiologically Active Substances of the Russian Academy of Sciences

Email: alaks@ipac.ac.ru
俄罗斯联邦, Severnyi proezd 1, Chernogolovka, 142432

T. Goreva

Institute of Physiologically Active Substances of the Russian Academy of Sciences

Email: alaks@ipac.ac.ru
俄罗斯联邦, Severnyi proezd 1, Chernogolovka, 142432

T. Epishina

Institute of Physiologically Active Substances of the Russian Academy of Sciences

Email: alaks@ipac.ac.ru
俄罗斯联邦, Severnyi proezd 1, Chernogolovka, 142432


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