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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 |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| WoS 742 .pdf Restricted Access | 102.98 kB | Adobe PDF | View/Open | |
| scopusresults 1145 .pdf Restricted Access | 131.75 kB | Adobe PDF | View/Open |
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