Organic hydroperoxides

Organic hydroperoxides

Organic compounds that contain a carbon bonded to an oxygen atom that is bonded to an alcohol functional group in the following structure: C-O-OH. Hydroperoxides are also known as peroxols.
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This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
tert-Butyl hydroperoxide is used as an initiator for radical polymerization and in various oxidation process such as sharpless epoxidation. It is involved in osmium catalyzed vicinal hydroxylation of olefins under alkaline conditions.
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In 1980, K.B. Sharpless and T. Katsuki discovered that the combination of titanium (IV) tetraisopropoxide, optically active diethyl tartrate, and tert-butyl hydroperoxide caused a wide variety of allylic alcohols to epoxidize in high yields.
While exploring the ring cleavage of cyclic ketones in 1899, A. Baeyer and V. Villiger discovered that ketones could be transformed into esters, and cyclic ketones into lactones or hydroxy acids, by using peroxyacids. This reaction became known as the Baeyer-Villiger oxidation.
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Generating and Detecting Reactive Oxygen Species—Section 18.2
Click Chemistry—Section 3.1