Copper-catalyzed aerobic oxidative coupling of ketones with P(O)–H compounds leading to β-ketophosphine oxides

Literature Information

Publication Date 2017-04-17
DOI 10.1039/C7QO00202E
Impact Factor 5.281
Authors

Qiang Zhang, Jianxin Ji, Wei Wei


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Abstract

A facile and efficient copper-catalyzed one-pot method for the construction of β-ketophosphine oxides has been developed via aerobic oxidative coupling of various ketones with P(O)–H compounds assisted by TBSOTf (t-butyldimethylsilyl triflate). Through this methodology, a series of β-ketophosphine oxides can be easily obtained in moderate to good yields with favorable functional group tolerance under very mild conditions. Isotope-labeling experiments suggested that the carbonyl oxygen atom of β-ketophosphine oxides originated from dioxygen.

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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