Cu(II)-Mediated C-H Amidation and Amination of Arenes: Exceptional Compatibility with Heterocycles

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	Cu(II)-Mediated C-H Amidation and Amination of Arenes: Exceptional Compatibility with Heterocycles
	Shang M(商明)1; Sun SZ(孙尚政)1; Dai HX(戴辉雄)1; Yu JQ(余金权)1
刊名	J. Am. Chem. Soc.
	2014
卷号	136 期号:9 页码:3354-3357
其他题名	对杂环异常兼容的二价铜参与的对芳烃的胺化及酰胺化
通讯作者	戴辉雄 ; 余金权
英文摘要	A Cu(OAc)(2)-mediated C-H amidation and amination of arenes and heteroarenes has been developed using a readily removable directing group. A wide range of sulfonamides, amides, and anilines function as amine donors in this reaction. Heterocycles present in both reactants are tolerated, making this a broadly applicable method for the synthesis of a family of inhibitors including 2-benzamidobenzoic acids and N-phenylaminobenzoates.
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/ja412880r
语种	英语
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/39044]
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.中科院上海有机化学研究所 2.美国斯克利普斯研究所
推荐引用方式 GB/T 7714	Shang M,Sun SZ,Dai HX,et al. Cu(II)-Mediated C-H Amidation and Amination of Arenes: Exceptional Compatibility with Heterocycles[J]. J. Am. Chem. Soc.,2014,136(9):3354-3357.
APA	商明,孙尚政,戴辉雄,&余金权.(2014).Cu(II)-Mediated C-H Amidation and Amination of Arenes: Exceptional Compatibility with Heterocycles.J. Am. Chem. Soc.,136(9),3354-3357.
MLA	商明,et al."Cu(II)-Mediated C-H Amidation and Amination of Arenes: Exceptional Compatibility with Heterocycles".J. Am. Chem. Soc. 136.9(2014):3354-3357.