Репозиторий научных и учебно-методических публикаций
ФГАОУ ВО «Северо-Кавказский федеральный университет»
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https://dspace.ncfu.ru/handle/20.500.12258/18169| Title: | Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine |
| Authors: | Aksenov, D. A. Аксенов, Д. А. Arutiunov, N. A. Арутюнов, Н. А. Gasanova, A. Z. Гасанова, А. З. Aksenov, N. A. Аксенов, Н. А. Aksenov, A. V. Аксенов, А. В. Rubin, M. A. Рубин, М. А. |
| Keywords: | Alkaloids;Rearrangement;Cascade reactions;Nitroalkanes;Total synthesis |
| Issue Date: | 2021 |
| Publisher: | Elsevier Ltd |
| Citation: | Aksenov, D. A.; Arutiunov, N. A.; Gasanova, A. Z.; Aksenov, N. A.; Aksenov, A. V.; Lower, C.; Rubin, M. A. Synthetic studies towards benzofuro[2,3-b]quinoline and 6H-indolo[2,3-b]quinoline cores: Total synthesis of norneocryptolepine and neocryptolepine // Tetrahedron Letters. - 2021. - Номер статьи 153395. - DOI 10.1016/j.tetlet.2021.153395 |
| Series/Report no.: | Tetrahedron Letters |
| Abstract: | An innovative acid-assisted cascade transformation of indoles with 2-nitrostyrenes was developed, allowing for the one-pot assembly of heterocyclic scaffolds with four fused rings. This strategy was subsequently employed for the concise total synthesis of two natural products, the alkaloids norneocryptolepine and neocryptolepine |
| URI: | http://hdl.handle.net/20.500.12258/18169 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| scopusresults 1871 .pdf Restricted Access | 615.38 kB | Adobe PDF | View/Open | |
| WoS 1252 .pdf Restricted Access | 85.14 kB | Adobe PDF | View/Open |
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