Advancements in Aminofluorination of Alkenes and Alkynes: Convenient Access to beta-Fluoroamines
Chen PH(陈品红); Liu GS(刘国生)
刊名Eur. J. Org. Chem.
2015
期号20页码:4295-4309
其他题名烯烃和炔烃的胺氟化反应: 快速合成β-氟代胺
通讯作者陈品红 ; 刘国生
英文摘要Direct aminofluorination of alkenes enables the convenient synthesis of beta-fluorinated amine compounds, which are important and valuable skeletons in medicinal chemistry. In recent years this research field has received much attention and significant advancements have been made by different approaches. In this review, recently disclosed methodologies for the production of beta-fluorinated amines, based on electrophilic and metal-catalyzed processes, are summarized and discussed. Finally, the outlook and perspectives for aminofluorination are also discussed.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/ejoc.201500231
语种英语
WOS记录号WOS:000358085100002
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/39621]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位中科院上海有机化学研究所, 金属有机化学国家重点实验室
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GB/T 7714
Chen PH,Liu GS. Advancements in Aminofluorination of Alkenes and Alkynes: Convenient Access to beta-Fluoroamines[J]. Eur. J. Org. Chem.,2015(20):4295-4309.
APA 陈品红,&刘国生.(2015).Advancements in Aminofluorination of Alkenes and Alkynes: Convenient Access to beta-Fluoroamines.Eur. J. Org. Chem.(20),4295-4309.
MLA 陈品红,et al."Advancements in Aminofluorination of Alkenes and Alkynes: Convenient Access to beta-Fluoroamines".Eur. J. Org. Chem. .20(2015):4295-4309.
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