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Fluoroalkylative Aryl Migration of Conjugated N-Arylsulfonylated Amides Using Easily Accessible Sodium Di- and Monofluoroalkanesulfinates
Alternative Title用易得的二氟和一氟烷基亚磺酸钠试剂对共轭N-芳基磺酰胺的氟烷基化-芳基迁移反应
He ZB(何正标); Tan P(谭平); Ni CF(倪传法); Hu JB(胡金波)
2015
Source PublicationOrg. Lett.
Volume17Issue:8Pages:1838-1841
AbstractFluorinated sulfinate salts RfSO2Na (R-f = CF2H, CF2Ph, and CH2F) have been prepared via NaBH4-mediated reduction of the corresponding benzo[d]thiazol-2-yl sulfones, and their synthetic application as di- and monofluoroalkyl radical precursors is demonstrated in the silver-catalyzed cascade fluoroalkylation/aryl migration/SO2 extrusion of conjugated N-arylsulfonylated amides.
Subtype论文
Subject Area氟化学
DOI10.1021/acs.orglett.5b00308
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000353314800006
Citation statistics
Cited Times:61[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39718
Collection中科院有机氟化学重点实验室
Corresponding AuthorHu JB(胡金波)
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
He ZB,Tan P,Ni CF,et al. Fluoroalkylative Aryl Migration of Conjugated N-Arylsulfonylated Amides Using Easily Accessible Sodium Di- and Monofluoroalkanesulfinates[J]. Org. Lett.,2015,17(8):1838-1841.
APA 何正标,谭平,倪传法,&胡金波.(2015).Fluoroalkylative Aryl Migration of Conjugated N-Arylsulfonylated Amides Using Easily Accessible Sodium Di- and Monofluoroalkanesulfinates.Org. Lett.,17(8),1838-1841.
MLA 何正标,et al."Fluoroalkylative Aryl Migration of Conjugated N-Arylsulfonylated Amides Using Easily Accessible Sodium Di- and Monofluoroalkanesulfinates".Org. Lett. 17.8(2015):1838-1841.
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