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直接三氟甲硫基化反应研究进展
Alternative TitleRecent Advances of Direct Trifluoromethylthiolation
张柯1; 徐修华1; 卿凤翎1
2015
Source Publication有机化学
Volume35Issue:3Pages:556-569
Other AbstractCompounds containing trifluoromethylthio group (SCF3) play an important role in pharmaceuticals, agrochemicals and materials due to its strong electron-withdrawing effect and extremely high lipophilicity. Very recently, trifluoromethylthiolation has received a great attention. In this review, the new progress of direct trifluoromethylthiolation is described. Furthermore, the synthetic challenge for trifluoromethylthiolation is also discussed.
Subtype论文
Subject Area氟化学
DOI10.6023/cjoc201501017
URL查看原文
Indexed BySCI
Language中文
WOS IDWOS:000353081600005
Citation statistics
Cited Times:52[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39721
Collection中科院有机氟化学重点实验室
Corresponding Author卿凤翎
Affiliation1.东华大学
2.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
张柯,徐修华,卿凤翎. 直接三氟甲硫基化反应研究进展[J]. 有机化学,2015,35(3):556-569.
APA 张柯,徐修华,&卿凤翎.(2015).直接三氟甲硫基化反应研究进展.有机化学,35(3),556-569.
MLA 张柯,et al."直接三氟甲硫基化反应研究进展".有机化学 35.3(2015):556-569.
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