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Updated: Jan 30, 2026

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Published on: August 27, 2015
Aza-Rubottom Oxidation: Synthetic Access to Primary α-Aminoketones
Zhe Zhou1, Qing-Qing Cheng1, László Kürti1
1Department of Chemistry , Rice University BioScience Research Collaborative , 6500 Main Street , Houston , Texas 77030 , United States.
Abstract:
An aza analogue of the Rubottom oxidation is reported. This facile transformation takes place at ambient temperature and directly converts silyl enol ethers to the corresponding primary α-aminoketones. The use of hexafluoroisopropanol (HFIP) as the solvent is essential for the success of this reaction. Overall this process is well-suited for the aza-functionalization and derivatization of complex organic molecules.
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