Direct ortho-Acylation of Azoxybenzenes with Aldehydes via Palladium-Catalyzed Regioselective C-H Bond Activation

被引:22
作者
Yi, Meiling [1 ]
Cui, Xiuling [1 ,2 ]
Zhu, Chongwei [1 ]
Pi, Chao [1 ]
Zhu, Weimin [1 ]
Wu, Yangjie [1 ]
机构
[1] Zhengzhou Univ, Henan Univ, Henan Key Lab Chem Biol & Organ Chem, Key Lab Appl Chem,Dept Chem, Zhengzhou 450052, Peoples R China
[2] Huaqiao Univ, Inst Mol Med, Sch Biomed Sci, Xiamen Key Lab Ocean & Gene Drugs, Xiamen 361021, Fujian, Peoples R China
基金
美国国家科学基金会;
关键词
aldehydes; azoxybenzenes; CH activation; ortho-acylation; palladium; DECARBOXYLATIVE ORTHO-ACYLATION; ALPHA-OXOCARBOXYLIC ACIDS; O-METHYL OXIMES; OXIDATIVE ORTHO-ACYLATION; LIQUID-CRYSTAL; DIRECT ACCESS; ORTHO-ALKOXYLATION; COMPOSITE FILMS; AZOBENZENE; ARYL;
D O I
10.1002/ajoc.201402251
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly efficient and convenient palladium catalyzed the ortho-acylation of azoxybenzenes has been developed. Easily available aldehydes were used as a cheap and ideal aroyl sources. This method provides a practical and direct pathway to synthesize 2-acylated azoxybenzenes in chemo- and regioselective manners via palladium-catalyzed CH bond activation. Various substituents on both coupling partners are tolerated well.
引用
收藏
页码:38 / 41
页数:4
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