Cyanarylation of Fluorinated Benzonitriles with Terephthalonitrile Dianion | Sciact

Cyanarylation of Fluorinated Benzonitriles with Terephthalonitrile Dianion Научная публикация

Журнал

ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ
ISSN: 0869-8538 , E-ISSN: 1817-1818

Вых. Данные

Год: 2022, Том: 30, Номер: 6, Страницы: 617-624 Страниц : 8 DOI: 10.15372/csd2022425

Ключевые слова

DICYANOBIPHENYLS, CYANARYLATION, FLUORINATED BENZONITRILES, NUCLEOPHILIC SUBSTITUTION OF FLUORINE

Авторы

PANTELEEVA E.V. ^1,2 , PESHKOV R.YU. ^1,2

Организации

1	Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences
2	Novosibirsk State University

The dianion generated by the reduction of terephthalonitrile with sodium in liquid ammonia arylates di- and trifluorobenzonitrites replacing the ortho- and para-fluorine atoms, as well as the para-hydrogen atom, with the para-cyanophenyl fragment. The orientation of the interaction, the structure of the resulting fluorinated 4,4′- and 2,4′-dicyanobiphenyls, and reaction productivity are determined by the location and number of fluorine atoms in the starting benzonitrile.

PANTELEEVA E.V. , PESHKOV R.Y.
Cyanarylation of Fluorinated Benzonitriles with Terephthalonitrile Dianion
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2022. V.30. N6. P.617-624. DOI: 10.15372/csd2022425 WOS РИНЦ OpenAlex

Пантелеева Е.В. , Пешков Р.Ю.
Цианарилирование фторированных бензонитрилов дианионом терефталонитрила
ХИМИЯ В ИНТЕРЕСАХ УСТОЙЧИВОГО РАЗВИТИЯ. 2022. DOI: 10.15372/KhUR2022425 РИНЦ OpenAlex

Web of science:	WOS:000899572500001
РИНЦ:	49923491
OpenAlex:	W4312690701

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