Alkene Syn- and Anti-Oxyamination with Malonoyl Peroxides
Jonathan M Curle1, Marina C Perieteanu1, Philip G Humphreys2
1Department of Pure and Applied Chemistry, WestCHEM, Thomas Graham Building , University of Strathclyde , 295 Cathedral Street , Glasgow G1 1XL , U.K.
Abstract:
Malonoyl peroxide 6 is an effective reagent for the syn- or anti-oxyamination of alkenes. Reaction of 6 and an alkene in the presence of O-tert-butyl-N-tosylcarbamate (R3 = CO2Bu) leads to the anti-oxyaminated product in up to 99% yield. Use of O-methyl-N-tosyl carbamate (R3 = CO2Me) as the nitrogen nucleophile followed by treatment of the product with trifluoroacetic acid leads to the syn-oxyaminated product in up to 77% yield. Mechanisms consistent with the observed selectivities are proposed.
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Radical Autoxidation


