SIOC OpenIR  > 中科院有机氟化学重点实验室
Iron-mediated Markovnikov-selective hydro-trifluoromethylthiolation of unactivated alkenes
Alternative Title铁促进的未活化烯烃马氏选择性的氢三氟甲硫基反应
Yang T(杨涛); Lv L(吕龙); Shen QL(沈其龙)
Source PublicationChem. Commun.
AbstractAn iron-mediated hydro-trifluoromethylthiolation of unactivated olefins under mild conditions was described for the first time. The reaction occurred to full conversion within 30 min at 0 degrees C and tolerates a variety of functional groups. Preliminary mechanistic studies suggested that the reaction proceeds via a free-radical pathway.
Subject Area氟化学
Indexed BySCI
WOS IDWOS:000351393600069
Citation statistics
Cited Times:56[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Corresponding AuthorLv L(吕龙); Shen QL(沈其龙)
Affiliation中科院上海有机化学研究所, 有机氟化学重点实验室
Recommended Citation
GB/T 7714
Yang T,Lv L,Shen QL. Iron-mediated Markovnikov-selective hydro-trifluoromethylthiolation of unactivated alkenes[J]. Chem. Commun.,2015,51(25):5479-5481.
APA 杨涛,吕龙,&沈其龙.(2015).Iron-mediated Markovnikov-selective hydro-trifluoromethylthiolation of unactivated alkenes.Chem. Commun.,51(25),5479-5481.
MLA 杨涛,et al."Iron-mediated Markovnikov-selective hydro-trifluoromethylthiolation of unactivated alkenes".Chem. Commun. 51.25(2015):5479-5481.
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