Selective cathodic reductions of 2,2%-furil in an aprotic medium, under constant potential, in the presence of equimolecular amounts of N-arylcarbonimidoyl dichlorides provide previously unknown 2-arylimino-4,5-di-2-furyl-1,3-dioxoles in high yields. These compounds were formed accompanied by minor
Electrochemical reduction of diaryl-1,2-diketones in the presence of carbonimidoyl dichlorides. A new method for the synthesis of enediol iminocarbonates
✍ Scribed by Antonio Guirado; Andrés Zapata; Jesús Gálvez
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 280 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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