The synthesis of imidazo[1,5-a]quinolines via a decarboxylative cyclization under metal-free conditions

被引：23
|
作者：
Yan, Zicong [1 ,2 ,3 ,4 ]
Wan, Changfeng [5 ]
Yang, Yu [1 ,2 ,3 ,4 ]
Zha, Zhenggen [1 ,2 ,3 ,4 ]
Wang, Zhiyong [1 ,2 ,3 ,4 ]
机构：
[1] Chinese Acad Sci, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Soft Matter Chem, Hefei 230026, Anhui, Peoples R China
[2] Chinese Acad Sci, Ctr Excellence Mol Synth, Hefei 230026, Anhui, Peoples R China
[3] Univ Sci & Technol China, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Hefei 230026, Anhui, Peoples R China
[4] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei 230026, Anhui, Peoples R China
[5] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China
来源：
RSC ADVANCES | 2018年 / 8卷 / 41期
基金：
中国国家自然科学基金;
关键词：
ALPHA-AMINO-ACIDS; C-H BONDS; OXIDATIVE AMINATION; HETEROCYCLIC CARBENES; CRIBROSTATIN; 6; HIGHLY POTENT; TRANSANNULATION; LIGANDS; IMIDAZO; CASCADE;
D O I：
10.1039/c8ra03786h
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
An iodine-mediated decarboxylative cyclization was developed from -amino acids and 2-methyl quinolines under metal-free conditions, affording a variety of imidazo[1,5-a]quinolines with moderate to good yields.
引用
收藏
页码：23058 / 23065
页数：8
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