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Copper-mediated intramolecular oxidative C-H/N-H cross-coupling of alpha-alkenoyl ketene N,S-acetals to synthesize pyrrolone derivatives
Huang, Fei1; Wu, Ping1; Wang, Liandi1; Chen, Jiping1; Sun, Chenglin1; Yu, Zhengkun1,2
Source PublicationCHEMICAL COMMUNICATIONS
2014
DOI10.1039/c4cc05837b
Volume50Issue:83Pages:12479-12481
Indexed BySCI ; IC ; CCR
SubtypeArticle
WOS HeadingsScience & Technology ; Physical Sciences
WOS SubjectChemistry, Multidisciplinary
WOS Research AreaChemistry
WOS KeywordSUBSTITUTED PYRROLIN-4-ONES ; BOND ACTIVATION ; HETEROCYCLES ; CYCLIZATION ; ACCESS ; AMIDES ; OXYGEN ; ACIDS
AbstractCuCl2 and CuBr2-mediated intramolecular oxidative C-H/N-H cross-coupling/halogenation of beta-thioalkyl-substituted alpha-alkenoyl ketene N,S-acetals occurred efficiently, affording 4-halo-5-thioalkyl-3-pyrrolones. Tunable C-S and C-halo bond transformations of the resultant pyrrolone derivatives led to highly functionalized N-heterocyclic compounds.
Language英语
WOS IDWOS:000342992000013
Citation statistics
Cited Times:24[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://cas-ir.dicp.ac.cn/handle/321008/145737
Collection中国科学院大连化学物理研究所
Affiliation1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
Recommended Citation
GB/T 7714
Huang, Fei,Wu, Ping,Wang, Liandi,et al. Copper-mediated intramolecular oxidative C-H/N-H cross-coupling of alpha-alkenoyl ketene N,S-acetals to synthesize pyrrolone derivatives[J]. CHEMICAL COMMUNICATIONS,2014,50(83):12479-12481.
APA Huang, Fei,Wu, Ping,Wang, Liandi,Chen, Jiping,Sun, Chenglin,&Yu, Zhengkun.(2014).Copper-mediated intramolecular oxidative C-H/N-H cross-coupling of alpha-alkenoyl ketene N,S-acetals to synthesize pyrrolone derivatives.CHEMICAL COMMUNICATIONS,50(83),12479-12481.
MLA Huang, Fei,et al."Copper-mediated intramolecular oxidative C-H/N-H cross-coupling of alpha-alkenoyl ketene N,S-acetals to synthesize pyrrolone derivatives".CHEMICAL COMMUNICATIONS 50.83(2014):12479-12481.
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