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Facile oxidation of aldehydes to acids and esters with Oxone
Benjamin R Travis1, Meenakshi Sivakumar, G Olatunji Hollist
1Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, USA.
Organic Letters
|March 28, 2003
Abstract:
[reaction: see text] A highly efficient, mild, and simple protocol is presented for the oxidation of aldehydes to carboxylic acids utilizing Oxone as the sole oxidant. Direct conversion of aldehydes in alcoholic solvents to their corresponding ester products is also reported. These reactions may prove to be valuable alternatives to traditional metal-mediated oxidations.