| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219746 | Tetrahedron | 2012 | 6 Pages |
Abstract
Oxidation of benzyl alcohols, benzyl halides, and alkylbenzenes to their corresponding oxidation products has been shown to be accomplished directly with oxone. The methodology that involves mere stirring/heating of the reactants and oxone in acetonitrile/water (1:1, v/v) is simple and practical, but is limited to substrates that do not contain sensitive functionalities and heteroaromatic rings.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Keshaba Nanda Parida, Samik Jhulki, Susovan Mandal, Jarugu Narasimha Moorthy,