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钴催化的通过 C-F 键活化的联芳基偶联反应,无需膦或 NHC 配体。

Cobalt-Catalyzed Biaryl Couplings via C-F Bond Activation in the Absence of Phosphine or NHC Ligands.

机构信息

College of Chemistry, Beijing Normal University , Beijing 100875, China.

出版信息

J Org Chem. 2017 Feb 3;82(3):1291-1300. doi: 10.1021/acs.joc.6b02354. Epub 2016 Oct 27.

Abstract

A highly general and selective Co-catalyzed biaryl coupling through C-F cleavage under phosphine or NHC-free conditions was described. A broad range of aryl fluorides including unactivated fluorides as well as those with sensitive functionalities could couple with various Ti(OEt)-mediated aryl Grignard reagents with high selectivity under the catalysis of CoCl/DMPU. Importantly, selective C-F bond activation couplings between two types of fluorines (difluorinated aromatics and on two different coupling partners) and in the presence of C-Cl or C-Br bonds could also be achieved.

摘要

本文报道了一种在无膦或 NHC 条件下通过 C-F 裂解实现的高通用性和高选择性的协同双芳基偶联反应。在 CoCl/DMPU 的催化作用下,各种 Ti(OEt)介导的芳基格氏试剂与广泛的芳基氟化物(包括未活化的氟化物以及具有敏感官能团的氟化物)都能以高选择性进行偶联。重要的是,两种类型的氟(二氟芳烃和两个不同的偶联伙伴之间)之间以及在 C-Cl 或 C-Br 键存在的情况下,C-F 键的选择性活化偶联也能实现。

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