SIOC OpenIR  > 中科院有机氟化学重点实验室
Chincona Alkaloid-Catalyzed Enantioselective Trifluoromethylthiolation of Oxindoles
Alternative Title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
Source PublicationChin. J. Chem.
Volume32Issue:8Pages:678-680
AbstractAn 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.
Subject Area氟化学
DOI10.1002/cjoc.201400392
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Indexed BySCI
Language英语
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Cited Times:27[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38858
Collection中科院有机氟化学重点实验室
Corresponding AuthorShen QL(沈其龙); Lv L(吕龙)
Affiliation中科院上海有机化学研究所
Recommended Citation
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.
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