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Silylation as a new strategy of the use of aliphatic nitro compounds in organic synthesis Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2001, Том: 50, Номер: 11, Страницы: 1936-1948 Страниц : 13 DOI: 10.1023/a:1015056024675
Авторы Tartakovsky V.A. 1 , Ioffe S.L. 1 , Dilman A.D. 1 , Tishkov A.A. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 119991, Moscow, Russian Federation

Реферат: Silylation of aliphatic nitro compounds is considered as a versatile multistage process. Due to activation of the β- and γ-carbon atoms of the initial nitro substrates, these reactions give rise to a series of products untypical of the traditional chemistry of nitro compounds. A new redox process proposed in the present study involves controlled incomplete reduction of the nitro group with simultaneous oxidation of the carbon skeleton of the initial aliphatic nitro compound.
Библиографическая ссылка: Tartakovsky V.A. , Ioffe S.L. , Dilman A.D. , Tishkov A.A.
Silylation as a new strategy of the use of aliphatic nitro compounds in organic synthesis
Russian Chemical Bulletin. 2001. V.50. N11. P.1936-1948. DOI: 10.1023/a:1015056024675 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000175056400004
Scopus: 2-s2.0-0035541759
OpenAlex: W2952494721
Цитирование в БД:
БД Цитирований
OpenAlex 13
Scopus 17
Web of science 19
Альметрики: