New Strategy for the Synthesis of Heterocycles via Copper-Catalyzed Oxidative Decarboxylative Amination of Glyoxylic Acid

被引:5
|
作者
Niu, Bin [1 ]
Li, Shaoqing [1 ]
Cui, Chang [1 ]
Yan, Yizhe [1 ]
Tang, Lin [3 ]
Wang, Jianyong [2 ]
机构
[1] Zhengzhou Univ Light Ind, Henan Key Lab Cold Chain Food Qual & Safety Contr, Henan Collaborat Innovat Ctr Food Prod & Safety, Sch Food & Biol Engn, Zhengzhou 450000, Henan, Peoples R China
[2] Qilu Univ Technol, Shandong Acad Sci, Sch Light Ind & Engn, Jinan 250353, Shandong, Peoples R China
[3] Xinyang Normal Univ, Coll Chem & Chem Engn, Xinyang 464000, Peoples R China
基金
中国国家自然科学基金;
关键词
Glyoxylic acid; Copper; Decarboxylation; C-N coupling; Heterocycles; BOND FORMATION; ARYL HALIDES; FUNCTIONALIZATION; QUINAZOLINONES; FORMYLATION; 1,3,5-TRIAZINES; HYDROFORMYLATION; ACTIVATION; INHIBITORS; QUINOLINE;
D O I
10.1002/ejoc.201901538
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A copper-catalyzed oxidative decarboxylative amination of glyoxylic acid with substrates having two nitrogen-nucleophilic sites was first demonstrated. Using this novel approach, 1,3,5-triazines, quinazolinones and quinazolines were obtained in up to 93 % yields. Notably, glyoxylic acid was employed as the C1 synthon for heterocycles. This strategy enriches the application of glyoxylic acid for the synthesis of valuable heterocycles.
引用
收藏
页码:7800 / 7803
页数:4
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