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Electrooxidative coupling of salts of nitro compounds with halide, nitrite, cyanide, and phenylsulfinate anions Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2005, Том: 54, Номер: 7, Страницы: 1585-1592 Страниц : 8 DOI: 10.1007/s11172-006-0007-7
Авторы Ilovaisky A.I. 1 , Merkulova V.M. 1 , Ogibin Yu.N. 1 , Nikishin G.I. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Реферат: Electrolysis of salts of primary and secondary nitro compounds (nitroethane, 1- and 2-nitropropanes, nitrocyclohexane, and nitrocycloheptane) in the presence of excess halide, nitrite, cyanide, and phenylsulfinate anions under undivided and divided amperostatic electrolysis conditions in a two-phase medium (CH2Cl2/H2O) produces geminal nitrohalides (35–85% yields), dinitro compounds (15–51%), nitronitriles (6–27%), and nitrosulfones (50–70%). The salts of secondary nitro compounds form the products of oxidative coupling with halide and phenylsulfinate anions under the undivided electrolysis conditions. In all other cases, divided electrolysis is required.
Библиографическая ссылка: Ilovaisky A.I. , Merkulova V.M. , Ogibin Y.N. , Nikishin G.I.
Electrooxidative coupling of salts of nitro compounds with halide, nitrite, cyanide, and phenylsulfinate anions
Russian Chemical Bulletin. 2005. V.54. N7. P.1585-1592. DOI: 10.1007/s11172-006-0007-7 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000234790700007
Scopus: 2-s2.0-31344470243
OpenAlex: W1970375953
Цитирование в БД:
БД Цитирований
OpenAlex 4
Scopus 6
Web of science 5
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