Iron-catalyzed three-component tandem process: a novel and convenient synthetic route to quinoline-2,4-dicarboxylates from arylamines, glyoxylic esters, and alpha-ketoesters
文献类型：期刊论文
| 作者 | Wei, Wei1,2; Wen, Jiangwei1,2; Yang, Daoshan1,2; Sun, Xuejun1,2; You, Jinmao1,2,3; Suo, Yourui3; Wang, Hua1,2 |
| 刊名 | tetrahedron
 |
| 出版日期 | 2013-12-16 |
| 卷号 | 69期号:50页码:10747-10751 |
| 关键词 | Iron catalysis Tandem reaction Arylamines alpha-Ketoesters Glyoxylic esters Quinoline-2,4-dicarboxylates |
| ISSN号 | 0040-4020 |
| 通讯作者 | you, jm (reprint author), qufu normal univ, key lab life organ anal, qufu 273165, shandong, peoples r china. |
| 中文摘要 | a new and convenient iron-catalyzed three-component tandem reaction of aromatic amines, glyoxylic esters, and alpha-ketoesters has been developed for the synthesis of quinoline-2,4-dicarboxylates under mild conditions. the present protocol, which utilizes cheap catalysts, readily-available starting materials and mild reaction conditions, provides an attractive approach to a series of functionalized quinoline derivatives with promising unique pharmaceutical, biological, and fluorescence-labeling applications. (c) 2013 elsevier ltd. all rights reserved. |
| 英文摘要 | a new and convenient iron-catalyzed three-component tandem reaction of aromatic amines, glyoxylic esters, and alpha-ketoesters has been developed for the synthesis of quinoline-2,4-dicarboxylates under mild conditions. the present protocol, which utilizes cheap catalysts, readily-available starting materials and mild reaction conditions, provides an attractive approach to a series of functionalized quinoline derivatives with promising unique pharmaceutical, biological, and fluorescence-labeling applications. (c) 2013 elsevier ltd. all rights reserved. |
| WOS标题词 | science & technology ; physical sciences |
| 类目[WOS] | chemistry, organic |
| 研究领域[WOS] | chemistry |
| 关键词[WOS] | quinoline derivatives ; biological evaluation ; substituted quinolines ; acridone alkaloids ; coenzyme pqq ; solvent-free ; aldehydes ; alkynes ; amines ; inhibitors |
| 收录类别 | SCI ; IC ; CCR |
| 语种 | 英语 |
| WOS记录号 | WOS:000327692000007 |
| 公开日期 | 2014-05-09 |
| 源URL | [http://ir.nwipb.ac.cn/handle/363003/3888]  |
| 专题 | 西北高原生物研究所_中国科学院西北高原生物研究所 |
| 作者单位 | 1.Qufu Normal Univ, Key Lab Life Organ Anal, Qufu 273165, Shandong, Peoples R China 2.Qufu Normal Univ, Key Lab Pharmaceut Intermediates & Anal Nat Med, Qufu 273165, Shandong, Peoples R China 3.Chinese Acad Sci, Northwest Inst Plateau Biol, Key Lab Evolut & Adaptat Plateau Biota, Xining 810001, Peoples R China |
| 推荐引用方式 GB/T 7714 | Wei, Wei,Wen, Jiangwei,Yang, Daoshan,et al. Iron-catalyzed three-component tandem process: a novel and convenient synthetic route to quinoline-2,4-dicarboxylates from arylamines, glyoxylic esters, and alpha-ketoesters[J]. tetrahedron,2013,69(50):10747-10751. |
| APA | Wei, Wei.,Wen, Jiangwei.,Yang, Daoshan.,Sun, Xuejun.,You, Jinmao.,...&Wang, Hua.(2013).Iron-catalyzed three-component tandem process: a novel and convenient synthetic route to quinoline-2,4-dicarboxylates from arylamines, glyoxylic esters, and alpha-ketoesters.tetrahedron,69(50),10747-10751. |
| MLA | Wei, Wei,et al."Iron-catalyzed three-component tandem process: a novel and convenient synthetic route to quinoline-2,4-dicarboxylates from arylamines, glyoxylic esters, and alpha-ketoesters".tetrahedron 69.50(2013):10747-10751. |
入库方式： OAI收割
来源：西北高原生物研究所
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