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Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles Научная публикация

Журнал Mendeleev Communications
ISSN: 0959-9436
Вых. Данные Год: 1994, Том: 4, Номер: 2, Страницы: 50-51 Страниц : 2 DOI: 10.1070/MC1994v004n02ABEH000343
Авторы Oleinik I.V. 1 , Zagulyaeva O.A. 1
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation

Реферат: An approach to the synthesis of previously unknown dihydroazinylidene nitroacetonitriles (derivatives of pyridine, pyrimidine, pyrazine and pyridazine) has been developed involving nitration of the corresponding dihydroazinylidene cyanoacetic esters at the side chain α-C-atom and dealkoxycarbonylation of the resulting products. © 1994, jointly by The Russian Academy of Sciences and The Royal Society of Chemistry (Turpion Ltd). All rights reserved.
Библиографическая ссылка: Oleinik I.V. , Zagulyaeva O.A.
Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles
Mendeleev Communications. 1994. V.4. N2. P.50-51. DOI: 10.1070/MC1994v004n02ABEH000343 WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 янв. 1994 г.
Идентификаторы БД:
Web of science: WOS:A1994NR82700007
Scopus: 2-s2.0-84930940046
РИНЦ: 30970584
OpenAlex: W2950995925
Цитирование в БД:
БД Цитирований
Scopus 4
Web of science 3
РИНЦ 3
OpenAlex 5
Альметрики: