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

Journal Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Output data Year: 2016, Volume: 65, Number: 7, Pages: 1814-1819 Pages count : DOI: 10.1007/s11172-016-1515-8
Tags photolysis; photocyclization; thermolysis; azides; 9,10-anthraquinones; phenols; 5H-naphtho[2,3-c]phenothiazine-8,13-diones; X-ray diffraction analysis
Authors Klimenko L. S. 1 , Sirazhetdinova N. S. 1 , Savel'ev V. A. 2 , Martyanov T. P. 3 , Korchagin D. V. 3
Affiliations
1 (Данные Web of science) Yugra State Univ, 16 Ul Chekhova, Khanty Mansiisk 6280012, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Prosp Akad Lavrenteva, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, Inst Problems Chem Phys, 1 Prosp Akad Semenova, Chernogolovka 142432, Moscow Region, Russia

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.
Cite: Klimenko L.S. , Sirazhetdinova N.S. , Savel'ev V.A. , Martyanov T.P. , Korchagin D.V.
Photochemical cyclocondensation of 1-arylthio-2-azidoanthraquinones with phenols
Russian Chemical Bulletin. 2016. V.65. N7. P.1814-1819. DOI: 10.1007/s11172-016-1515-8 WOS Scopus РИНЦ OpenAlex
Original: Клименко Л.И. , Сиражетдинова Н.С. , Савельев В.А. , Мартьянов Т.П. , Корчагин Д.В.
Фотохимическая циклоконденсация 2-азидо-1-арилтиоантрахинонов с фенолами
Известия Академии наук. Серия химическая.(RUSS CHEM B+). 2016. №7. С.1814-1819. РИНЦ
Dates:
Published print: Jul 1, 2016
Published online: Mar 16, 2017
Identifiers:
Web of science: WOS:000398191000021
Scopus: 2-s2.0-85015387896
Elibrary: 29495208
OpenAlex: W2601838988
Citing:
DB Citing
Web of science 1
Scopus 1
Elibrary 2
OpenAlex 1
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