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Oxidation of N-benzyl groups

✍ 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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✦ Synopsis


Abstract

The additive reactivity of 2,6,8,12‐tetraacetyl‐4, 10‐dibenzyl‐2,4,6,8,10,12‐hexazatetracyclo [5.5.0.0^5.9^. 0^3.11^] dodecane (3) in several conditions was studied. It was found that the N‐benzyl 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.


πŸ“œ SIMILAR VOLUMES


Improved Preparation of Ξ±,N-Diphenylnitr
✍ John W. Gorrod; Nigel J. Gooderham πŸ“‚ Article πŸ“… 1986 πŸ› John Wiley and Sons 🌐 English βš– 346 KB πŸ‘ 1 views

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