The reaction of benzofuroxan with p-anisylazide: Trapping of the o-dinitroso-intermediate
β Scribed by A.B. Bulacinski; E.F.V. Scriven; H. Suschitzky
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 107 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
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 could apply this method to demonstrate chemicallv the intermediacy of the c-dinitrosocompound.
π SIMILAR VOLUMES
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