Nitroylides 2. Reaction of sulfonium dinitroylides with electrophiles Научная публикация
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Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science
ISSN: 2376-8444 , E-ISSN: 0568-5230 |
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| Вых. Данные | Год: 1977, Том: 26, Номер: 1, Страницы: 120-125 Страниц : 6 DOI: 10.1007/bf00921507 | ||
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Реферат:
1. Sulfonium dinitroylides are cleaved at the bond by electrophiles such as halogens (chlorine, bromine, bromine chloride), sulfuryl chloride, hydrogen halides (chloride and bromide), giving the corresponding di- or monohalodinitromethanes. 2. Phenylsulfenyl chloride reacts with , forming dinitrobis(phenylthio)methane and dtnitrophenylthiomethane. 3. Compounds containing a positive halogen (N-haloamides, N-chloroalkylnitramines, BrONO2, SO2FCl, CH3CO2C1) react with to give the corresponding dihalodinitromethanes. 4. Electrophiles (chlorine, bromine, phenylsulfenyl chloride) are capable of cleaving the bond of dinitromethylsulfonium salts, forming the corresponding monosubstituted dinitromethane, ClCH(NO2)2, BrCH(NO2)2, and PhSCH(NO2)2. On the basis of our results we propose a scheme for the reaction of with phenylsulfenyl chloride and compounds containing a positive halogen.
Библиографическая ссылка:
Shevelev S.A.
, Semenov V.V.
, Fainzil'berg A.A.
Nitroylides 2. Reaction of sulfonium dinitroylides with electrophiles
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1977. Т.26. №1. С.120-125. DOI: 10.1007/bf00921507 OpenAlex
Nitroylides 2. Reaction of sulfonium dinitroylides with electrophiles
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1977. Т.26. №1. С.120-125. DOI: 10.1007/bf00921507 OpenAlex
Идентификаторы БД:
| OpenAlex: | W2328722392 |
Цитирование в БД:
| БД | Цитирований |
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| OpenAlex | Нет цитирований |