Nickel-Catalyzed Intramolecular Nucleophilic Addition of Aryl Halides to Aryl Ketones for the Synthesis of Benzofuran Derivatives

被引：3
|
作者：
Zhu, Xiao-Rui [1 ]
Deng, Chen-Liang [1 ,2 ]
机构：
[1] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Peoples R China
[2] Wenzhou Univ, Inst New Mat & Ind Technol, Wenzhou 325035, Peoples R China
来源：
SYNTHESIS-STUTTGART | 2021年 / 53卷 / 10期
基金：
中国国家自然科学基金;
关键词：
nickel; zinc powder; intramolecular addition; cyclization; benzofuran; CROSS-COUPLING REACTION; GRIGNARD-REAGENTS; FUNCTIONALIZATION; ACTIVATION; EFFICIENT; INSERTION; INDOLES;
D O I：
10.1055/s-0040-1706662
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A nickel-catalyzed intramolecular nucleophilic addition reaction of aryl halides to aryl ketones for the formation of benzofuran derivatives has been developed. A number of substrates bearing electron-donating or electron-withdrawing groups were subjected to the standard reaction conditions, giving the corresponding products in moderate to good yields.
引用
收藏
页码：1842 / 1848
页数：7
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