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铜催化的烯烃的三氟甲基芳基化反应:芳基硼酸和 CF3+试剂的相互活化。

Copper-catalyzed intermolecular trifluoromethylarylation of alkenes: mutual activation of arylboronic acid and CF3+ reagent.

机构信息

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , 345 Lingling Road, Shanghai, China , 200032.

出版信息

J Am Chem Soc. 2014 Jul 23;136(29):10202-5. doi: 10.1021/ja504458j. Epub 2014 Jul 8.

Abstract

A novel copper-catalyzed intermolecular trifluoromethylarylation of alkenes is developed using less active ether-type Togni's reagent under mild reaction conditions. Various alkenes and diverse arylboronic acids are compatible with these conditions. Preliminary mechanistic studies reveal that a mutual activation process between arylboronic acid and CF3(+) reagent is essential. In addition, the reaction might involve a rate-determining transmetalation, and the final aryl C-C bond is derived from reductive elimination of the aryl(alkyl)Cu(III) intermediate.

摘要

发展了一种新颖的铜催化的烯烃的三氟甲基芳基化反应,使用不太活泼的醚型 Togni 试剂,在温和的反应条件下进行。各种烯烃和不同的芳基硼酸都与这些条件兼容。初步的机理研究表明,芳基硼酸和 CF3(+)试剂之间的相互活化过程是必不可少的。此外,反应可能涉及一个速率决定的转金属过程,最终的芳基 C-C 键来自芳基(烷基)Cu(III)中间体的还原消除。

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