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Reactions catalyzed by a binuclear copper complex: selective oxidation of alkenes to carbonyls with O2

Abstract

Terminal alkenes were selectivitely cleavaged into ketones and aldehydes catalysed by a binuclear copper catalyst bearing simple salicylate ligand with O2 as oxidant. The reaction was carried out under an atmosphere of O2 balloon with 0.5 mol% of catalyst and could be performed at a gram scale, providing a convenient and practical method for the cleavage of terminal alkenes into carbonyl compounds.

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Publication details

The article was received on 27 Aug 2017, accepted on 06 Oct 2017 and first published on 06 Oct 2017


Article type: Communication
DOI: 10.1039/C7CY01757J
Citation: Catal. Sci. Technol., 2017, Accepted Manuscript
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    Reactions catalyzed by a binuclear copper complex: selective oxidation of alkenes to carbonyls with O2

    Y. Liu, D. Xue, C. Li, J. Xiao and C. Wang, Catal. Sci. Technol., 2017, Accepted Manuscript , DOI: 10.1039/C7CY01757J

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