Oxidative Trifluoromethylthiolation of Terminal Alkynes with AgSCF3: A Convenient Approach to Alkynyl Trifluoromethyl Sulfides

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	Oxidative Trifluoromethylthiolation of Terminal Alkynes with AgSCF3: A Convenient Approach to Alkynyl Trifluoromethyl Sulfides
	Zhu SQ(朱圣卿)1; Xu XH(徐修华)1; Qing FL(卿凤翎)1
刊名	Eur. J. Org. Chem.
	2014
期号	21 页码:4453-4456
其他题名	末端炔烃与AgSCF3的氧化三氟甲硫基化: 一个方便途径制备炔三氟甲硫基化合物
通讯作者	卿凤翎
英文摘要	A new method for the efficient synthesis of alkynyl trifluoromethyl sulfides was developed. By combining AgSCF3 and NCS in N,N-dimethylacetamide, an electrophilic active intermediate was produced, which was then treated with a variety of terminal alkynes to afford the corresponding trifluoromethanesulfenylated products in moderate to excellent yields.
学科主题	氟化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1002/ejoc.201402533
语种	英语
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/38848]
专题	上海有机化学研究所_中科院有机氟化学重点实验室
作者单位	1.中科院上海有机化学研究所 2.东华大学
推荐引用方式 GB/T 7714	Zhu SQ,Xu XH,Qing FL. Oxidative Trifluoromethylthiolation of Terminal Alkynes with AgSCF3: A Convenient Approach to Alkynyl Trifluoromethyl Sulfides[J]. Eur. J. Org. Chem.,2014(21):4453-4456.
APA	朱圣卿,徐修华,&卿凤翎.(2014).Oxidative Trifluoromethylthiolation of Terminal Alkynes with AgSCF3: A Convenient Approach to Alkynyl Trifluoromethyl Sulfides.Eur. J. Org. Chem.(21),4453-4456.
MLA	朱圣卿,et al."Oxidative Trifluoromethylthiolation of Terminal Alkynes with AgSCF3: A Convenient Approach to Alkynyl Trifluoromethyl Sulfides".Eur. J. Org. Chem. .21(2014):4453-4456.