Manganese dioxide oxidation of aryl 1,2-diaminoimidazoles
โ Scribed by Nakajima, Masayuki; Hisada, Ryuki; Anselme, Jean Pierre
- Book ID
- 126790888
- Publisher
- American Chemical Society
- Year
- 1978
- Tongue
- English
- Weight
- 464 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Cyclopentenolones of type (1) constitute the alcohol fragment of the natural rethrins. Knowledge of their oxidation reactions is of general interest in connection with the rapid and little understood deterioration of such insecticidal films. During a study of the reaction between manganese dioxide a
Several structurally differentiated N,N-dialkylhydroxylamines were oxidised to the corresponding nitrones using MnO 2 . Manganese dioxide revealed an efficient and mild reagent for oxidation of hydroxylamines, showing a level of regioselectivity comparable to HgO. Its non-toxicity makes MnO 2 the re