Copper-Catalyzed Trifluoromethylthiolation of Aryl Halides with Diverse Directing Groups

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	Copper-Catalyzed Trifluoromethylthiolation of Aryl Halides with Diverse Directing Groups
	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
刊名	Org. Lett.
	2014
卷号	16 期号:15 页码:3942-3945
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
通讯作者	叶金星 ; 刘国生
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.
学科主题	金属有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1021/ol501742a
语种	英语
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/39086]
专题	上海有机化学研究所_金属有机化学国家重点实验室
作者单位	1.华东理工大学 2.中科院上海有机化学研究所
推荐引用方式 GB/T 7714	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.
APA	徐佳斌,慕欣,陈品红,叶金星,&刘国生.(2014).Copper-Catalyzed Trifluoromethylthiolation of Aryl Halides with Diverse Directing Groups.Org. Lett.,16(15),3942-3945.
MLA	徐佳斌,et al."Copper-Catalyzed Trifluoromethylthiolation of Aryl Halides with Diverse Directing Groups".Org. Lett. 16.15(2014):3942-3945.