## Abstract Several representatives of natural flavonoids and their synthetic nitroβderivatives have been investigated by polarography and electron paramagnetic resonance (EPR) spectroscopy under electrochemical reduction in acetonitrile, dimethylformamide (DMF), dimethylsulfoxide (DMSO) or 1,2βdim
β¦ LIBER β¦
Polyhalogenated Radical-anions
β Scribed by R.D. Chambers; D.T. Clark; C.R. Sargent; F.G. Drakesmith
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 148 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Electrochemical reduction of polyhalogenopyridines gives products from which structures of intermediate radical anions are inferred; the results agree with calculations. Fully halogenated aromatic compounds provide interesting orientation problems in nucleophilic aromatic substitution, that are analogous to the well known orientation problems of electrophilic aromatic substitution.
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