Conversion of non-terminal alkenes into secondary alkyl t-butyl peroxides by peroxymercuriation and reduction with tributyltin hydride

Abstract
S-Butyl, 3-hexyl, cyclopentyl, and cyclohexyl t-butyl peroxides have been prepared in yields of 63, 24, 59, and 61%, respectively, by reducing with tributyltin hydride the peroxymercurials derived from the corresponding symmetrical alkenes.

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