Formation of 4,5-dihydro-1,2,4-triazoles during rearrangement of O-acetyl derivatives of 1,2-hydroxylaminohydrazones and thiosemicarbazones Научная публикация
| Журнал |
Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353 |
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| Вых. Данные | Год: 1986, Том: 22, Номер: 3, Страницы: 287-291 Страниц : DOI: 10.1007/BF00514996 | ||
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Реферат:
Acylation of phenylhydrazone, semicarbazone, and thiosemicarbazones of 1,2-hydroxyl-amino-ketones containing a hydroxylamine group at the tertiary carbon atom, by acetic anhydride, leads to products of O-acylation at the hydroxylamine group, which in alkali medium rearrange to form 4,5-dihydro-1,2,4-triazoles. © 1986 Plenum Publishing Corporation.
Библиографическая ссылка:
Belova N.V.
, Volodarskii L.B.
, Tikhonov A.Y.
Formation of 4,5-dihydro-1,2,4-triazoles during rearrangement of O-acetyl derivatives of 1,2-hydroxylaminohydrazones and thiosemicarbazones
Chemistry of Heterocyclic Compounds. 1986. V.22. N3. P.287-291. DOI: 10.1007/BF00514996 Scopus РИНЦ OpenAlex
Formation of 4,5-dihydro-1,2,4-triazoles during rearrangement of O-acetyl derivatives of 1,2-hydroxylaminohydrazones and thiosemicarbazones
Chemistry of Heterocyclic Compounds. 1986. V.22. N3. P.287-291. DOI: 10.1007/BF00514996 Scopus РИНЦ OpenAlex
Даты:
| Опубликована в печати: | 1 мар. 1986 г. |
Идентификаторы БД:
| Scopus: | 2-s2.0-34250124270 |
| РИНЦ: | 30839845 |
| OpenAlex: | W2025691744 |
Цитирование в БД:
Пока нет цитирований