Trapping an intermediate of the polonovski reaction
β Scribed by Y. Hayashi; Y. Nagano; S. Hongyo; K. Teramura
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 179 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Previous studies using n.m.r. have indicated that benzofuroxan may tautomerise via g-dinitrosobenzene as shown, and the activation energy of this process has been measured'. We recently reported the trapping of triplet arvlnitrenes bv some nitrosoarenes in boilino bromobenzeneL and thought that we
The deearboxylafion of 1,3-dimethylorotic acid was investigated to study the nature of the reaction intermediate. 6-Benzyl-l,3-dimethyluracil was isolated when the deearboxylation was carried out in benzyl bromide, indicating.the involvement of a carbon-6 centered nucleophilic intermediate in the re