| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223058 | Tetrahedron | 2010 | 6 Pages |
Abstract
The oxidation of some substituted monohydric phenols, containing electron-withdrawing substituents at the ortho position to the phenolic group, with [hydroxy(tosyloxy)iodo]benzene (HTIB, Koser's reagent) leads to novel tosyloxylation of aromatic ring, thereby offering a convenient synthesis of hitherto unknown 4-tosyloxy-2-substituted phenols.
Graphical abstractThe oxidation of some substituted monohydric phenols, containing electron-withdrawing substituents at the ortho position to the phenolic group, with [hydroxy(tosyloxy)iodo]benzene (HTIB, Koser's reagent) leads to novel tosyloxylation of aromatic ring, thereby offering a convenient synthesis of hitherto unknown 4-tosyloxy-2-substituted phenols.Download full-size image
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Physical Sciences and Engineering
Chemistry
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![A novel and convenient approach for tosyloxylation of aromatic ring of some ortho-substituted phenolic compounds using [hydroxy(tosyloxy)iodo]benzene](/preview/png/5223058.png "First Page Preview: A novel and convenient approach for tosyloxylation of aromatic ring of some ortho-substituted phenolic compounds using [hydroxy(tosyloxy)iodo]benzene")
Authors
Om Prakash, Manoj Kumar, Rajesh Kumar,