Synthesis of α-trifluoromethyl ethanone oximes via the three-component reaction of aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent

文献情報

出版日 2019-10-01

DOI 10.1039/C9QO00940J

インパクトファクター 5.281

著者

Kui Lu, Quan Li, Liangshuo Ji, Erbing Hua, Yujie Dai, Xia Zhao

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要旨

A mild and simple protocol for the synthesis of α-trifluoromethylated ethanone oximes from aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent was developed under transition metal-free conditions. In this three-component reaction, tert-butyl nitrite was employed not only as the oxidant but also as the oxime source. A range of α-trifluoromethylated ethanone oximes were obtained, indicating the wide substrate scope of the reaction.

掲載誌

Organic Chemistry Frontiers

CiteScore: 7.8

自己引用率: 8.7%

年間論文数: 724

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

Synthesis of α-trifluoromethyl ethanone oximes via the three-component reaction of aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent

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