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镍催化α-卤代羰基化合物与芳基硼酸的温和芳基化反应。

Ni-catalyzed mild arylation of alpha-halocarbonyl compounds with arylboronic acids.

作者信息

Liu Chao, He Chuan, Shi Wei, Chen Mao, Lei Aiwen

机构信息

College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei 430072, China.

出版信息

Org Lett. 2007 Dec 20;9(26):5601-4. doi: 10.1021/ol702456z. Epub 2007 Dec 4.

DOI:10.1021/ol702456z
PMID:18052180
Abstract

A simple yet powerful Ni catalyst can be used to promote direct arylations of alpha-halocarbonyl compounds, including a range of esters, amides, and ketones, with various arylboronic acids under mild conditions. The method tolerates beta-hydrogens and functional groups in the substrates and offers reactivity and selectivity profiles that are complementary to those found in the well-established Buchwald-Hartwig approach.

摘要

一种简单却强大的镍催化剂可用于在温和条件下促进α-卤代羰基化合物(包括一系列酯、酰胺和酮)与各种芳基硼酸的直接芳基化反应。该方法能耐受底物中的β-氢和官能团,并提供与成熟的布赫瓦尔德-哈特维希方法互补的反应活性和选择性特征。

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