A review of the chemical literature reveals a number of addition reactions to the nitroso functional group which appear analogous in many respects to those observed for carbonyl compounds. 1 It is also recognized that nitroso compounds are excellent acceptors of electrons from anionic species to yi
The reaction of N-sulfonyl sulfilimine with cyanide ion in DMSO
β Scribed by S. Oae; T. Aida; K. Tsujihara; N. Furukawa
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 202 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Recently we reported that N-eulfonyl sulfilimines having a-protons react with D&30 or diethyl sulfoxide at elevated temperflture giving unsymmetric disulfides in substantial yields. 1) The mechanism of the above reaction is postulated to involve the initial formation of an equilibrium mixture of ylide and ylene followed by the nucleophilic attack by sulfoxide oxygen.
π SIMILAR VOLUMES
We have found that substituent groups and solvents may have striking effects on the rates of bimolecular reactions involving nucleophiles and photoexcited nitroaromatic compounds. As representative cases, data on reactions of cyanide ion and 4-nitroanisole, l-nitronaphtbalene. and 4-methoxy-1-nitron