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Acylation of 1-hydroxyamino-2-hydroxyiminoethanes with α-halo acid chlorides and the preparation of 1-hydroxy-2-oxotetrahydropyrazine 4-oxides Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1984, Том: 20, Номер: 1, Страницы: 97-102 Страниц : DOI: 10.1007/BF00505860
Авторы Tikhonov A. Ya. , Volodarskii L. B. , Belova N. V.
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Novosibirsk, Russian Federation

Реферат: The acylation of 1-hydroxyamino-2-hydroxyiminoethanes with α-halo acid chlorides has given the products of N- and O-acylation at the hydroxyamino group. The action of bases on the products of N-acylation - N-(2-hydroxyiminoalkyl)-2-halohydroxamic acids - has given, depending on the conditions, 1-hydroxy-2-oxo-1,2,3,6- or -1,2,5,6-tetrahydropyrazine 4-oxides and 1,2-oxazetidin-3-ones. © 1984 Plenum Publishing Corporation.
Библиографическая ссылка: Tikhonov A.Y. , Volodarskii L.B. , Belova N.V.
Acylation of 1-hydroxyamino-2-hydroxyiminoethanes with α-halo acid chlorides and the preparation of 1-hydroxy-2-oxotetrahydropyrazine 4-oxides
Chemistry of Heterocyclic Compounds. 1984. V.20. N1. P.97-102. DOI: 10.1007/BF00505860 Scopus РИНЦ OpenAlex
Идентификаторы БД:
Scopus: 2-s2.0-34250132238
РИНЦ: 30918860
OpenAlex: W176820531
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Scopus 1
OpenAlex 2
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