Oxidation of N-benzyl groups
β Scribed by Wen-Ge Qiu; Shu-Sen Chen; Yong-Zhong Yu
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 218 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0256-7660
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β¦ Synopsis
Abstract
The additive reactivity of 2,6,8,12βtetraacetylβ4, 10βdibenzylβ2,4,6,8,10,12βhexazatetracyclo [5.5.0.0^5.9^. 0^3.11^] dodecane (3) in several conditions was studied. It was found that the Nβbenzyl groups in compound 3 could be oxidized to benzoyl groups by Cr(VI) reagents, and could be removed by cerium ammonium nitrate (CAN), meanwhile nitroamine products were given.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
A simple and rapid method for the oxidation of secondary anilines to a,N-diphenylnitrones and the subsequent reduction to secondary N-benzyl-N-phenylhydroxylamines is described. Verbesserte Synthese von a,N.Diphenylnitronen und N-Benzyi-N-phenylhydroxylaminen durch direkte Oxidation von sekundΓ€ren