Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12258/21936
Title: | A Convenient Way to Quinoxaline Derivatives through the Reaction of 2-(3-Oxoindolin-2-yl)-2-phenylacetonitriles with Benzene-1,2-diamines |
Authors: | Aksenov, A. V. Аксенов, А. В. Arutiunov, N. A. Арутюнов, Н. А. Aksenov, D. A. Аксенов, Д. А. Samovolov, A. V. Самоволов, А. В. Kurenkov, I. A. Куренков, И. А. Aksenov, N. A. Аксенов, Н. А. Aleksandrova, E. A. Александрова, Е. А. Momotova, D. S. Момотова, Д. С. Rubin, M. A. Рубин, М. А. |
Keywords: | Cyclization;Microwave synthesis;Quinoxalines;Chemical structure |
Issue Date: | 2022 |
Publisher: | MDPI |
Citation: | Aksenov, A.V., Arutiunov, N.A., Aksenov, D.A., Samovolov, A.V., Kurenkov, I.A., Aksenov, N.A., Aleksandrova, E.A., Momotova, D.S., Rubin, M. A Convenient Way to Quinoxaline Derivatives through the Reaction of 2-(3-Oxoindolin-2-yl)-2-phenylacetonitriles with Benzene-1,2-diamines // International Journal of Molecular Sciences. - 2022. - Volume 23. - Issue 19. - Номер статьи 11120. - DOI10.3390/ijms231911120 |
Series/Report no.: | International Journal of Molecular Sciences |
Abstract: | Microwave-assisted reaction between 2-(3-oxoindolin-2-yl)-2-phenylacetonitriles andbenzene-1,2-diamines leads to the high-yielding formation of the corresponding quinoxalines as sole, easily isolaable products. The featured transformation involves unusual extrusion of phenylacetonitrile molecule and could be performed in a short sequence starting from commonly available indoles and nitroolefins. |
URI: | http://hdl.handle.net/20.500.12258/21936 |
Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
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scopusresults 2375 .pdf Restricted Access | 2.1 MB | Adobe PDF | View/Open | |
WoS 1483 .pdf Restricted Access | 114.35 kB | Adobe PDF | View/Open |
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