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https://dspace.ncfu.ru/handle/20.500.12258/4247| Title: | Metal-free ring expansion of indoles with nitroalkenes: A simple, modular approach to 3-substituted 2-quinolones |
| Authors: | Aksenov, A. V. Аксенов, А. В. Smirnov, A. N. Смирнов, А. Н. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. Rubin, M. A. Рубин, М. А. |
| Keywords: | Ketones;Arylhydrazines;Cascade transformations;Electron-rich arenes;Modular approach;Polyphosphoric acids;Ring expansion;Synthesis (chemical) |
| Issue Date: | 2015 |
| Publisher: | Royal Society of Chemistry |
| Citation: | Aksenov, A.V., Smirnov, A.N., Aksenov, N.A., Aksenova, I.V., Matheny, J.P., Rubin, M. Metal-free ring expansion of indoles with nitroalkenes: A simple, modular approach to 3-substituted 2-quinolones // RSC Advances. - 2015. - Volume 5. - Issue 12. - Pages 8647-8656 |
| Series/Report no.: | RSC Advances |
| Abstract: | 3-Substituted 2-quinolones are obtained via a novel metal-free transannulation reaction of 2-nitroolefins with 2-substituted indoles in polyphosphoric acid. This acid-mediated cascade transformation operates via the ANRORC (Addition of Nucleophile, Ring Opening, and Ring Closure) mechanism and can be used in combination with the Fisher indole synthesis to offer a practical three-component hetero-annulation approach to 2-quinolones from arylhydrazines, 2-nitroalkenes, and acetophenone. An alternative entry to this chemistry employing the alkylation of electron-rich arenes and hetarenes with 1-(2-indolyl)-2-nitroalkene has also been demonstrated |
| URI: | http://hdl.handle.net/20.500.12258/4247 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| scopusresults 793 .pdf Restricted Access | 64.46 kB | Adobe PDF | View/Open | |
| WoS 513 .pdf Restricted Access | 44.32 kB | Adobe PDF | View/Open |
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