Copper-Mediated Intramolecular Oxidative C-H/C-H Cross-Coupling of alpha-Oxo Ketene N,S-Acetals for Indole Synthesis
Huang, Fei1; Wu, Ping1; Wang, Liandi1; Chen, Jiping1; Sun, Chenglin1; Yu, Zhengkun1,2
刊名journal of organic chemistry
2014-11-07
卷号79期号:21页码:10553-10560
英文摘要cucl2-mediated intramolecular c-h/c-h cross-dehydrogenative coupling (cdc) of thioalkyl-substituted a-acetyl or alpha-aroyl ketene n,s-acetals afforded 2-thioalkyl indoles. tunable c-s bond transformations of the resultant indoles led to highly functionalized n-heterocyclic compounds. a beta-thioalkyl is necessary to activate the n,s-acetal substrate and enable the cdc reaction to occur, and the relevant mechanism studies revealed that the cdc reaction follows a radical pathway.
WOS标题词science & technology ; physical sciences
类目[WOS]chemistry, organic
研究领域[WOS]chemistry
关键词[WOS]n-aryl enamines ; bond activation ; cyclization ; anilines ; efficient ; functionalization ; heterocycles ; annulation ; catalysis ; oxidant
收录类别SCI ; IC
语种英语
WOS记录号WOS:000344638200056
公开日期2016-05-09
内容类型期刊论文
源URL[http://cas-ir.dicp.ac.cn/handle/321008/145747]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.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
推荐引用方式
GB/T 7714
Huang, Fei,Wu, Ping,Wang, Liandi,et al. Copper-Mediated Intramolecular Oxidative C-H/C-H Cross-Coupling of alpha-Oxo Ketene N,S-Acetals for Indole Synthesis[J]. journal of organic chemistry,2014,79(21):10553-10560.
APA Huang, Fei,Wu, Ping,Wang, Liandi,Chen, Jiping,Sun, Chenglin,&Yu, Zhengkun.(2014).Copper-Mediated Intramolecular Oxidative C-H/C-H Cross-Coupling of alpha-Oxo Ketene N,S-Acetals for Indole Synthesis.journal of organic chemistry,79(21),10553-10560.
MLA Huang, Fei,et al."Copper-Mediated Intramolecular Oxidative C-H/C-H Cross-Coupling of alpha-Oxo Ketene N,S-Acetals for Indole Synthesis".journal of organic chemistry 79.21(2014):10553-10560.
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