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Reductive activation of arenes: XIX. Mechanism and some synthetic applications of the alkylation of phthalodinitrile radical anion Научная публикация

Журнал Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Вых. Данные Год: 2006, Том: 42, Номер: 9, Страницы: 1280-1288 Страниц : DOI: 10.1134/S1070428006090053
Авторы Panteleeva E. V. , Vaganova T. A. , Luk'yanets E. A. , Shteingarts V. D.
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Div, Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
3 (Данные Web of science) State Res Ctr, Res Inst Organ Intermediate Prod & Dyes, Moscow, Russia

Реферат: Using cyclopropylmethyl bromide as mechanism-sensitive reagent, it was shown that the reaction of phthalonitrile radical anion with alkyl halides in liquid ammonia involves electron transfer. The effects of the nature of alkyl bromide and counterion in the radical anion salt and reaction conditions on the ratio of 2-alkylbenzonitrile, 4-alkylphthalonitrile, and 2,5-dialkylbenzonitrile were studied. Phthalodinitrile radical anion was found to undergo dimerization with formation of biphenyl-2,'3',4'-tricarbonitrile. The examined transformations may underlie syntheses of phthalonitriles modified at the 4-position.
Библиографическая ссылка: Panteleeva E.V. , Vaganova T.A. , Luk'yanets E.A. , Shteingarts V.D.
Reductive activation of arenes: XIX. Mechanism and some synthetic applications of the alkylation of phthalodinitrile radical anion
Russian Journal of Organic Chemistry. 2006. V.42. N9. P.1280-1288. DOI: 10.1134/S1070428006090053 WOS Scopus РИНЦ OpenAlex
Оригинальная: Пантелеева Е.В. , Ваганова Т.А. , Лукьянец Е.А. , Штейнгарц В.Д.
Восстановительная активация аренов xix/ механизм и некоторые синтетические приложения алкилирования анион-радикала фталодинитрила
Журнал органической химии (RUSS J ORG CHEM+). 2006. Т.42. №9. С.1301-1309. РИНЦ
Даты:
Опубликована в печати: 1 сент. 2006 г.
Идентификаторы БД:
Web of science: WOS:000241615500005
Scopus: 2-s2.0-33750001163
РИНЦ: 13519640
OpenAlex: W1971277993
Цитирование в БД:
БД Цитирований
Web of science 10
Scopus 8
РИНЦ 7
OpenAlex 7
Альметрики: