## 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
Regiochemistry and mechanism of oxidation of N-benzyl-N-alkylhydroxylamines to nitrones
β Scribed by Azfar Hassan; Mohammed I. M. Wazeer; Mohammed T. Saeed; Mohammad N. Siddiqui; Sk. Asrof Ali
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 111 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0894-3230
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π SIMILAR VOLUMES
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
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The kinetics of the oxidation of aspirin (ASP) by bromamine-T (BAT), N-bromosuccinimide (NBS), and N-bromophthalimide (NBP) has been studied in aqueous perchloric acid at The oxidation reaction follows identical kinetics with first-order in [oxidant], 303 K. fractional-order in [ASP], and inverse f