Transition-Metal-Free TEMPO Catalyzed Aerobic Oxidation of Alcohols to Carbonyls Using an Efficient Br2 Equivalent under Mild Conditions

An effective transition-metal-free catalytic system is developed for aerobic oxidations of alcohols. Using catalytic amount of bromide-bromate coupling, H2SO4, and NaNO2, together with 2,2,6,6-tetramethylpiperidine N-oxyl radical (TEMPO) in the presence of air, various alcohols could be converted in...

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Veröffentlicht in:Chinese journal of chemistry 2013-06, Vol.31 (6), p.794-798
Hauptverfasser: Zhang, Jie, Jiang, Zengqiang, Zhao, Dan, He, Guozhen, Zhou, Shuangli, Han, Shiqing
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Sprache:eng
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Zusammenfassung:An effective transition-metal-free catalytic system is developed for aerobic oxidations of alcohols. Using catalytic amount of bromide-bromate coupling, H2SO4, and NaNO2, together with 2,2,6,6-tetramethylpiperidine N-oxyl radical (TEMPO) in the presence of air, various alcohols could be converted into the corresponding aldehydes or ketones in good to excellent isolated yields under mild conditions.
ISSN:1001-604X
1614-7065
DOI:10.1002/cjoc.201300052