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镍催化双亲性 α-溴代烷基硼酸酯的反转芳基化反应。

Nickel-Catalyzed Umpolung Arylation of Ambiphilic α-Bromoalkyl Boronic Esters.

机构信息

Institute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology, Av. Països Catalans 16, 43007, Tarragona, Spain.

Catalan Institution for Research and Advanced Studies (ICREA), Passeig Lluïs Companys, 23, 08010, Barcelona, Spain.

出版信息

Angew Chem Int Ed Engl. 2018 Mar 26;57(14):3622-3625. doi: 10.1002/anie.201712428. Epub 2018 Mar 1.

Abstract

A nickel-catalyzed reductive arylation of ambiphilic α-bromoalkyl boronic esters with aryl halides is described. This platform provides an unrecognized opportunity to promote the catalytic umpolung reactivity of ambiphilic reagents with aryl halides, thus unlocking a new cross-coupling strategy that complements existing methods for the preparation of densely functionalized alkyl-substituted organometallic reagents from simple and readily accessible precursors.

摘要

本文描述了镍催化的双亲性α-溴代烷基硼酸酯与芳基卤化物的还原芳基化反应。该平台提供了一个未被认识到的机会,可以促进双亲性试剂与芳基卤化物的催化反转反应性,从而解锁一种新的交叉偶联策略,为从简单易得的前体制备稠合官能化的烷基取代有机金属试剂提供了补充现有方法。

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