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Pyrimidines. 73. Synthesis of acetylpyrimidines Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1981, Том: 17, Номер: 7, Страницы: 710-714 Страниц : DOI: 10.1007/BF00506042
Авторы Naumenko I. I. , Mikhaleva M. A. , Mamaev V. P.
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Реферат: It is shown that the use of benzene as the solvent in the preparation of 2- and 4-acetylpyrimidines from cyanopyrimidines via the Grignard reaction makes this reaction a practical method for the preparation of pyrimidinyl ketones. Preparatively convenient methods for the preparation of 4-acetylpyrimidine from 4-ethylpyrimidine through the α-oximino derivative and 5-acetylpyrimidine from 4,6-dichloro derivatives of pyrimidine are proposed. © 1982 Plenum Publishing Corporation.
Библиографическая ссылка: Naumenko I.I. , Mikhaleva M.A. , Mamaev V.P.
Pyrimidines. 73. Synthesis of acetylpyrimidines
Chemistry of Heterocyclic Compounds. 1981. V.17. N7. P.710-714. DOI: 10.1007/BF00506042 Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 июл. 1981 г.
Идентификаторы БД:
≡ Scopus: 2-s2.0-34250224523
≡ РИНЦ: 30992338
≡ OpenAlex: W2950960399
Альметрики: