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/20.500.12258/18095| Title: | Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion |
| Authors: | Demidov, O. P. Демидов, О. П. |
| Keywords: | Recyclization;Azepino[4; benzo[d ]azepines;5-b]indoles;Azepinones;Betaines;Dithiocarboxylates;Iminium salts;Isoquinolinium salts;Thioamides |
| Issue Date: | 2021 |
| Publisher: | Elsevier Ltd |
| Citation: | Zubenko, A. A.; Sochnev, V. S.; Kartsev, V. G.; Divaeva L. N.; Demidov, O. P.; Klimenko A. I.; Bodryakov A. N.; Bodryakova M. A.; Borodkin, G. S.; Morkovnik, A. S. Systems with annulated thioxo azepinone moiety: an access through heterocyclic carbodithioate ring expansion // Mendeleev Communications. - 2021. - Том 31. - Выпуск 4. - Стр.: 545 - 547 |
| Series/Report no.: | Mendeleev Communications |
| Abstract: | New 1-oxo-2-thioxo-1,2,4,5-tetrahydrobenz[d]azepine and 1-oxo-2-thioxo-1,2,4,5-tetrahydroazepino[4,5-b]indole derivatives were conveniently obtained by the novel recyclization reaction of (methylthio) carbonothioylsubstituted heterocyclic quaternary salts with expansion of the dihydropyridine ring |
| URI: | http://hdl.handle.net/20.500.12258/18095 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| scopusresults 1857 .pdf Restricted Access | 234.54 kB | Adobe PDF | View/Open | |
| WoS 1228 .pdf Restricted Access | 189.15 kB | Adobe PDF | View/Open |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.