Photochemical cyclocondensation of 1-arylthio-2-azidoanthraquinones with phenols


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Photolysis of 1-arylthio-2-azidoanthraquinones in DMSO in the presence of phenols leads to the formation of 5H-naphtho[2,3-c]phenothiazine-8,13-diones, in which the nitrogen atom is covalently bonded with the phenyl ring of the introduced phenol. As a result, poorly available polycyclic phenothiazine derivatives were obtained in one step in high yields. The cyclo-condensation with phenols was found to proceed only photochemically.

About the authors

L. S. Klimenko

Yugra State University

Author for correspondence.
Email: L_Klimenko@ugrasu.ru
Russian Federation, 16 ul. Chekhova, Khanty-Mansiisk, 6280012

N. S. Sirazhetdinova

Yugra State University

Email: L_Klimenko@ugrasu.ru
Russian Federation, 16 ul. Chekhova, Khanty-Mansiisk, 6280012

V. A. Savel’ev

N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences

Email: L_Klimenko@ugrasu.ru
Russian Federation, 9 prosp. Akad. Lavrent’eva, Novosibirsk, 630090

T. P. Martyanov

Institute of Problems of Chemical Physics, Russian Academy of Sciences

Email: L_Klimenko@ugrasu.ru
Russian Federation, 1 prosp. Akad. Semenova, Chernogolovka, Moscow Region, 142432

D. V. Korchagin

Institute of Problems of Chemical Physics, Russian Academy of Sciences

Email: L_Klimenko@ugrasu.ru
Russian Federation, 1 prosp. Akad. Semenova, Chernogolovka, Moscow Region, 142432


Copyright (c) 2016 Springer Science+Business Media New York

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies