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Tautomerism of derivatives of azines. 16. Tautomerism of acylmethylpyrazines and -quinoxalines Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Вых. Данные Год: 1987, Том: 23, Номер: 12, Страницы: 1339-1342 Страниц : 4 DOI: 10.1007/BF00472261
Авторы Mainagashev I.Ya. 1 , Lapachev V.V. 1 , Fedotov M.A. 1 , Mamaev V.P. 1
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Реферат: The tautomeric equilibria of acylmethylpyrazines and -quinoxalines in chloroform were studied by 1H, 14N, and 17O NMR spectroscopy. It was shown that keto-enol tautomerism is realized in the acylmethylpyrazine series. Annelation leads to the development of an ylidene tautomer in the acylmethylquinoxaline series. A marked dependence of the position of the intrachelate equilibrium on the character of the solvent was observed. © 1988 Plenum Publishing Corporation.
Библиографическая ссылка: Mainagashev I.Y. , Lapachev V.V. , Fedotov M.A. , Mamaev V.P.
Tautomerism of derivatives of azines. 16. Tautomerism of acylmethylpyrazines and -quinoxalines
Chemistry of Heterocyclic Compounds. 1987. V.23. N12. P.1339-1342. DOI: 10.1007/BF00472261 Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 дек. 1987 г.
Идентификаторы БД:
Scopus: 2-s2.0-34250092627
РИНЦ: 30867102
OpenAlex: W1987709918
Цитирование в БД: Пока нет цитирований
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