Chincona Alkaloid-Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles

	Chincona Alkaloid-Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles
其他题名	奎宁催化的氧化吲哚的不对称三氟甲硫基化研究
	Yang T(杨涛); Shen QL(沈其龙); Lv L(吕龙)
	2014
发表期刊	Chin. J. Chem.
卷号	32 期号:8 页码:678-680
摘要	An organocatalytic asymmetric trifluoromethylthiolation of 3-aryl or 3-alkyloxindoles employing a trifluoromethyl-substituted thioperoxide as the electrophilic trifluoromethylthiolating reagent was described. Reactions occurred in good to excellent enantioselectivities to generate oxindoles with a SCF3-substituted quaternary chiral center.
学科领域	氟化学
DOI	10.1002/cjoc.201400392
URL	查看原文
收录类别	SCI
语种	英语
引用统计
文献类型	期刊论文
条目标识符	http://ir.sioc.ac.cn/handle/331003/38858
专题	中科院有机氟化学重点实验室
通讯作者	Shen QL(沈其龙); Lv L(吕龙)
作者单位	中科院上海有机化学研究所
推荐引用方式 GB/T 7714	Yang T,Shen QL,Lv L. Chincona Alkaloid-Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles[J]. Chin. J. Chem.,2014,32(8):678-680.
APA	杨涛,沈其龙,&吕龙.(2014).Chincona Alkaloid-Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles.Chin. J. Chem.,32(8),678-680.
MLA	杨涛,et al."Chincona Alkaloid-Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles".Chin. J. Chem. 32.8(2014):678-680.