Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/10138
Title: Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines
Authors: Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Arutiunov, N. A.
Арутюнов, Н. А.
Malyuga, V. V.
Малюга, В. В.
Ovcharov, S. N.
Овчаров, С. Н.
Rubin, M. A.
Рубин, М. А.
Keywords: Amines;Aliphatic diamines;Aromatic amines;Benzimidazoles;En-route;Imidazolines;Nitroalkanes;Phosphorous acid;Synthetic methodology;Paraffins
Issue Date: 2019
Publisher: Royal Society of Chemistry
Citation: Aksenov, A.V., Aksenov, N.A., Arutiunov, N.A., Malyuga, V.V., Ovcharov, S.N., Rubin, M. Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines // RSC Advances. - 2019. - Volume 9. - Issue 67. - Pages 39458-39465
Series/Report no.: RSC Advances
Abstract: A novel synthetic methodology for the assembly of imidazolines via an unusual reaction between nitroalkanes and aliphatic 1,2-diamines in the presence of phosphorous acid is described. In contrast to the related highly efficient preparation of benzimidazoles from aromatic amines, this process represents a major synthetic challenge and for a long time was elusive. Analysis of the method limitations is provided
URI: http://hdl.handle.net/20.500.12258/10138
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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