期刊
JOURNAL OF FLUORINE CHEMISTRY
卷 161, 期 -, 页码 134-141出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2014.01.016
关键词
Nucleophilic trifluoromethylation; Fluoroform; Trimethylsilyltrifluoromethane; Fluorinated sulfones; Fluorinated sulfoxides; Fluorinated sulfides
资金
- Argentine Research National Council (Conicet)
- University of Buenos Aires
- Agencia Nacional de Promocion Cientifica y Tecnica (ANPCyT)
Nucleophilic trifluoromethylation and perfluoroalkylation reactions have been the outstanding approach during the last few decades to effect fluoroalkyl group addition or substitution reactions. In most instances, perfluoroalkyl-metal species participate at the beginning of the reactions. In this account, however, the latest nucleophilic non-metal assisted or uncatalyzed trifluoromethylation and perfluoroalkylation reactions of substrates bearing biological relevance will be discussed. (C) 2014 Elsevier B.V. All rights reserved.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据