中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Structure-Reactivity Relationship of Trifluoromethanesulfenates: Discovery of an Electrophilic Trifluoromethylthiolating Reagent

文献类型:期刊论文

作者Shao XX(邵欣欣); Xu CF(徐春发); Lv L(吕龙); Shen QL(沈其龙)
刊名J. Org. Chem.
出版日期2015
卷号80期号:6页码:3012-3021
其他题名结构活性相关-三氟甲基次磺酸酯: 新型亲电三氟甲硫基化试剂的研制
通讯作者吕龙 ; 沈其龙
英文摘要A family of electrophilic trifluoromethanesulfenates was prepared. Structure-reactivity relationship studies showed that the substituted groups on the aryl ring of the trifluoromethylthiolating reagent did not have an obvious influence on their reactivities. A simplified electrophilic trifluoromethylthiolating reagent 1c was then identified that can react with a wide range of nucleophiles such as Grignard reagents, arylboronic acids, alkynes, indoles, beta-ketoesters, oxindoles, and sodium sulfinates under mild reaction conditions. A variety of functional groups were tolerated under these conditions.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/jo502645m
语种英语
WOS记录号WOS:000351558400006
源URL[http://ir.sioc.ac.cn/handle/331003/39716]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
作者单位中科院上海有机化学研究所, 有机氟化学重点实验室
推荐引用方式
GB/T 7714
Shao XX,Xu CF,Lv L,et al. Structure-Reactivity Relationship of Trifluoromethanesulfenates: Discovery of an Electrophilic Trifluoromethylthiolating Reagent[J]. J. Org. Chem.,2015,80(6):3012-3021.
APA 邵欣欣,徐春发,吕龙,&沈其龙.(2015).Structure-Reactivity Relationship of Trifluoromethanesulfenates: Discovery of an Electrophilic Trifluoromethylthiolating Reagent.J. Org. Chem.,80(6),3012-3021.
MLA 邵欣欣,et al."Structure-Reactivity Relationship of Trifluoromethanesulfenates: Discovery of an Electrophilic Trifluoromethylthiolating Reagent".J. Org. Chem. 80.6(2015):3012-3021.

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来源:上海有机化学研究所

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