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Reaction of 1,3- hydroxylamino oximes with formaldehyde, acetaldehyde, and acetone Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1977, Том: 13, Номер: 2, Страницы: 201-207 Страниц : DOI: 10.1007/BF00497878
Авторы Tikhonov A. Ya. , Volodarskii L. B.
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Реферат: The products of condensation of 1,3-hydroxylamino oximes with formaldehyde have 1-hydroxy-1,2,5,6-tetrahydropyrimidine 3-oxide (cyclic form) structures, the products of condensation with acetone have N-(3-oximino-substituted)-α,α-dimethylnitrone (open form) structures, and the products of condensation with acetaldehyde exist in solution in the form of a tautomeric mixture of the open and cyclic forms. The products of condensation of alkyl-aromatic 1,3-hydroxylamino oximes with acetaldehyde have N-(3-oximino-substituted)-α-nitrone (open form) structures. © 1977 Plenum Publishing Corporation.
Библиографическая ссылка: Tikhonov A.Y. , Volodarskii L.B.
Reaction of 1,3- hydroxylamino oximes with formaldehyde, acetaldehyde, and acetone
Chemistry of Heterocyclic Compounds. 1977. V.13. N2. P.201-207. DOI: 10.1007/BF00497878 Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 февр. 1977 г.
Идентификаторы БД:
Scopus: 2-s2.0-34250292654
РИНЦ: 30992365
OpenAlex: W1981076022
Цитирование в БД:
БД Цитирований
Scopus 1
РИНЦ 1
OpenAlex 1
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