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学科主题: 氟化学 ; 金属有机化学
题名: Efficient Synthesis of 2-Fluoromethylated Quinolines via Copper-Catalyzed Alkynylation and Cyclization of Fluorinated Imidoyl Iodides
其他题名: 通过铜催化的亚胺酰卤的炔基化和环化反应高效合成2-氟烷基取代的喹啉化合物
作者: Li S(李珊) ; Yuan YF(袁雅芬) ; Zhu JT(祝江涛) ; Xie HB(谢海波) ; Chen ZX(陈资衔) ; Wu YM(吴永明)
通讯作者: 吴永明
刊名: Adv. Synth. Catal.
发表日期: 2010
卷: 352, 期:10, 页:1582-1586
收录类别: SCI
部门归属: 中国科学院上海有机化学研究所; 华中科技大学
英文摘要: 2-Fluoromethylated quinolines were synthesized through the reaction of N-aryl-fluorinated imidoyl iodides with terminal alkynes in good yields by the catalysis of copper(I) iodide (CuI) alone.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000280657900003
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/25145
Appears in Collections:中科院有机氟化学重点实验室_期刊论文

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Recommended Citation:
Li S,Yuan YF,Zhu JT,et al. Efficient Synthesis of 2-Fluoromethylated Quinolines via Copper-Catalyzed Alkynylation and Cyclization of Fluorinated Imidoyl Iodides[J]. Adv. Synth. Catal.,2010,352(10):1582-1586.
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