## Abstract~hemical interaction of quinoneimines with substituted l&dihydropyridine (Hantxsch ester) in aprotic solvents has been modelled by electrochemical mechanistic studies. Conclusions about the mechanism of the chemical reaction have been based on results of the study of electrochemical red
✦ LIBER ✦
Electrochemical reduction of N-aryl- and N-arylsulphonylbenzoquinoneimines in acetonitrile—II. Electron affinity and relationship between oxidation and reduction potentials
✍ Scribed by J. Stradiņš; V. Glezer; B. Turovska; E. Markava; J. Freimanis
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 637 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0013-4686
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## Electrochemical reduction of 1,6benzoquinonemonoimine derivatives have been studied in acetonitrile. As a rule reduction of monoimines proceeds in two steps, the lirst of them results in the formation of an anion-radical. Introduction of sulpho-group between the quinoneimine and aryl moieties l