4.7 Article

Palladium-Catalyzed Direct Oxidation of Alkenes with Molecular Oxygen: General and Practical Methods for the Preparation of 1,2-Diols, Aldehydes, and Ketones

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JOURNAL OF ORGANIC CHEMISTRY
卷 75, 期 7, 页码 2321-2326

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AMER CHEMICAL SOC
DOI: 10.1021/jo100125q

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  1. National Natural Foundation of China [20625205, 20772034, 20932002]

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1,2-Diols, aldehydes, and ketones are important intermediates in chemical synthesis, and alkenes are possible precursors for 1,2-diols, aldehydes, and ketones. Herein, novel and environmentally benign methods for palladium-catalyzed dihydroxylation and oxidative cleavage of olefins with oxygen as sole oxidant are presented. The cleavage reactions were performed with acid as additive ill aqueous solution, whereas 1,2-diols were formed in the presence of base. A broad substrate scope has been demonstrated allowing monosubstituted aromatic and aliphatic terminal alkenes, 1,2-disubstituted, and 1,1-disubstituted olefins. The cleavage reactions of dioxo-Pd(II) complexes implicate 1,2-diol might act as a key intermediate of olefin cleavage.

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