The oxygenation of cyclopalladated N,N-dimethylbenzylamine derivatives with tert-butyl hydroperoxide
β Scribed by Paul L. Alsters; Herman T. Teunissen; Jaap Boersma; Gerard van Koten
- Book ID
- 104589231
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 184 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0165-0513
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β¦ Synopsis
Abstract
Cyclopalladated N,Nβdimethylbenzylamine complexes can be oxygenated with tertβbutyl hydroperoxide to the corresponding phenolates in good yield (> 80%); the rate of oxygenation is highly enhanced by increasing the nucleophilicity of the metal center or by addition of a vanadium catalyst.
π SIMILAR VOLUMES
The Reactions of 3,6-Di-tert-butyl-1,2-benzoquinone and 3,6-Ditert-butylcatechol with tert-Butyl Hydroperoxide. -The reaction of the title quinone (I) as well as its corresponding catechol with tert-butyl hydroperoxide in aprotic solvents results in ring oxidation accompanied by ring expansion furn