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Iron-catalyzed three-component tandem process: a novel and convenient synthetic route to quinoline-2,4-dicarboxylates from arylamines, glyoxylic esters, and alpha-ketoesters
Wei, Wei1,2; Wen, Jiangwei1,2; Yang, Daoshan1,2; Sun, Xuejun1,2; You, Jinmao1,2,3; Suo, Yourui3; Wang, Hua1,2; You, JM (reprint author), Qufu Normal Univ, Key Lab Life Organ Anal, Qufu 273165, Shandong, Peoples R China.
2013-12-16
Source PublicationTETRAHEDRON
ISSN0040-4020
Volume69Issue:50Pages:10747-10751
SubtypeArticle
AbstractA 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.; 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.
KeywordIron Catalysis Tandem Reaction Arylamines Alpha-ketoesters Glyoxylic Esters Quinoline-2 4-dicarboxylates
WOS HeadingsScience & Technology ; Physical Sciences
WOS KeywordQUINOLINE DERIVATIVES ; BIOLOGICAL EVALUATION ; SUBSTITUTED QUINOLINES ; ACRIDONE ALKALOIDS ; COENZYME PQQ ; SOLVENT-FREE ; ALDEHYDES ; ALKYNES ; AMINES ; INHIBITORS
Indexed BySCI ; IC ; CCR
Language英语
WOS Research AreaChemistry
WOS SubjectChemistry, Organic
WOS IDWOS:000327692000007
Citation statistics
Cited Times:15[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://210.75.249.4/handle/363003/3888
Collection中国科学院西北高原生物研究所
Corresponding AuthorYou, JM (reprint author), Qufu Normal Univ, Key Lab Life Organ Anal, Qufu 273165, Shandong, Peoples R China.
Affiliation1.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
Recommended Citation
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.,...&You, JM .(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.
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