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 anal
β¦ LIBER β¦
Phosphonitrilic radical anions
β Scribed by Allcock, Harry R.; Birdsall, W. J.
- Book ID
- 126198032
- Publisher
- American Chemical Society
- Year
- 1969
- Tongue
- English
- Weight
- 302 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0002-7863
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## 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