Репозиторий научных и учебно-методических публикаций
Северо-Кавказский федеральный университет
Please use this identifier to cite or link to this item:
https://dspace.ncfu.ru/handle/20.500.12258/3532| Title: | Nitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indoles |
| Authors: | Aksenov, A. V. Аксенов, А. В. Aksenov, N. A. Аксенов, Н. А. Aksenov, D. A. Аксенов, Д. А. Khamraev, V. F. Хамраев, В. Ф. Rubin, M. A. Рубин, М. А. |
| Keywords: | Indole;Cycloaddition of indoles |
| Issue Date: | 2018 |
| Publisher: | NLM (Medline) |
| Citation: | Aksenov, A.V., Aksenov, N.A., Aksenov, D.A., Khamraev, V.F., Rubin, M. Nitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indoles // Chemical communications (Cambridge, England). - 2018. - Volume 54. - Issue 94. - Pages 13260-13263 |
| Series/Report no.: | Chemical communications |
| Abstract: | An unusual reactivity of nitrostyrenes in phosphorous acid was discovered, which permits the employment of these readily available synthons as 1,4-CCNO-dipole surrogates in a highly diastereoselective (4+1)-cycloaddition of indoles to afford 4'H-spiro[indole-3,5'-isoxazoles] in a diastereomerically pure form |
| URI: | http://hdl.handle.net/20.500.12258/3532 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| WoS 416 .pdf Restricted Access | 106.75 kB | Adobe PDF | View/Open | |
| scopusresults 631.pdf Restricted Access | 112.34 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.