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学科主题: 金属有机化学
题名: Copper-Catalyzed Trifluoromethylthiolation of Aryl Halides with Diverse Directing Groups
其他题名: 铜催化含各种导向基团的芳基卤化物的硫三氟甲基化反应
作者: Xu JB(徐佳斌)1; Mu X(慕欣)1; Chen PH(陈品红)1; Ye JX(叶金星)1; Liu GS(刘国生)1
通讯作者: 叶金星 ; 刘国生
刊名: Org. Lett.
发表日期: 2014
DOI: 10.1021/ol501742a
卷: 16, 期:15, 页:3942-3945
收录类别: SCI
英文摘要: The expansion of cross-coupling components in Cu-catalyzed C-X bond forming reactions have received much attention recently. A novel Cu-catalyzed trifluoromethylthioladon of aryl bromides and iodides with the assistance of versatile directing groups such as pyridyl, methyl ester, amide, imine and oxime was reported. CuBr was used as the catalyst, and 1,10-phenanthroline as the ligand. By changing the solvent from acetonitrile to DMF, the coupling process could even take place at room temperature.
语种: 英语
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/39086
Appears in Collections:金属有机化学国家重点实验室_期刊论文

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作者单位: 1.华东理工大学
2.中科院上海有机化学研究所

Recommended Citation:
Xu JB,Mu X,Chen PH,et al. Copper-Catalyzed Trifluoromethylthiolation of Aryl Halides with Diverse Directing Groups[J]. Org. Lett.,2014,16(15):3942-3945.
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