| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1375050 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
The hypervalent iodine-catalyzed oxylactonization of ketocarboxylic acids to ketolactones was achieved in the presence of iodobenzene (10 mol %), p-toluenesulfonic acid monohydrate (20 mol %) and meta-chloroperbenzoic acid as a stoichiometric co-oxidant.
Graphical abstractThe hypervalent iodine-catalyzed oxylactonization of ketocarboxylic acids to ketolactones was achieved in the presence of iodobenzene (10 mol %), TsOH (20 mol %) and m-CPBA as stoichiometric co-oxidant.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Muhammet Uyanik, Takeshi Yasui, Kazuaki Ishihara,