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Nickel-Catalyzed Cross-Coupling of Functionalized Difluoromethyl Bromides and Chlorides with Aryl Boronic Acids: A General Method for Difluoroalkylated Arenes

机译:镍催化的功能化二氟甲基溴化物和氯化物与芳基硼酸的交叉偶联:二氟烷基化芳烃的通用方法

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摘要

Transition-metal-catalyzed difluoroalkylation of aromatics remains challenging despite the importance of difluoroalkylated arenes in medicinal chemistry. Herein, the first successful example of nickel-catalyzed difluoroalkylation of aryl boronic acids is described. The reaction allows access to a variety of functionalized difluoromethyl bromides and chlorides, and paves the way to highly cost-efficient synthesis of a wide range of difluoroalkylated arenes. The notable features of this protocol are its high generality, excellent functional-group compatibility, low-cost nickel-catalyst, and practicality for gram-scale production, thus providing a facile method for applications in drug discovery and development.
机译:尽管二氟烷基化的芳烃在药物化学中很重要,但过渡金属催化的芳烃的二氟烷基化仍然具有挑战性。在此,描述了镍催化的芳基硼酸的二氟烷基化的第一个成功实例。该反应允许获得各种官能化的二氟甲基溴化物和氯化物,并为高成本效益的各种二氟烷基化芳烃的合成铺平了道路。该协议的显着特征是它的通用性强,出色的官能团兼容性,低成本的镍催化剂以及克级生产的实用性,因此为药物发现和开发中的应用提供了一种简便的方法。

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