Репозиторий научных и учебно-методических публикаций
Северо-Кавказский федеральный университет
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https://dspace.ncfu.ru/handle/123456789/31842| Title: | Synthesis of 2,4-Disubstituted Quinolines by the Reaction of Propargylic Alcohols with Anilines in a Polyphosphoric Acid Medium |
| Authors: | Aksenov, A. V. Аксенов, А. В. Aksenov, N. A. Аксенов, Н. А. Akulova, A. S. Акулова, А. С. Makieva, D. C. Макиева, Д. С. Aksenova, I. V. Аксенова, И. В. Arutiunov, N. A. Арутюнов, Н. А. Aksenov, D. A. Аксенов, Д. А. |
| Keywords: | Acetylenes;The Friedel-crafts reaction;Heterocyclization;Kucherov reaction;Propargyl alcohols;Quinolines |
| Issue Date: | 2025 |
| Publisher: | Pleiades Publishing |
| Citation: | Aksenov, A. V., Aksenov, N. A., Akulova, A. S., Makieva, D. C., Aksenova, I. V., Arutiunov, N. A., Aksenov, D. A. Synthesis of 2,4-Disubstituted Quinolines by the Reaction of Propargylic Alcohols with Anilines in a Polyphosphoric Acid Medium // Russian Journal of Organic Chemistry. - 2025. - 61 (6). - pp. 1141 – 1147. - DOI: 10.1134/S1070428025602687 |
| Series/Report no.: | Russian Journal of Inorganic Chemistry |
| Abstract: | A novel method for quinoline synthesis based on the interaction of propargylic alcohols with anilines in the presence of polyphosphoric acid (PPA) has been developed. It has been discovered that propargylic alcohols in a PPA medium are capable of hydrolyzing into chalcones. The use of PPA in ethyl acetate solution has been demonstrated for the first time. |
| URI: | https://dspace.ncfu.ru/handle/123456789/31842 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| scopusresults 3648.pdf Restricted Access | 126.56 kB | Adobe PDF | View/Open | |
| WoS 2183.pdf Restricted Access | 114.14 kB | Adobe PDF | View/Open |
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