Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/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

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