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- W2736545116 abstract "There have been significant developments in the area of perfluoroalkyl group transfer using silicon reagents, specifically in nucleophilic trifluoromethylation. The mild and versatile activation conditions bestow significant synthetic prowess to the silicon reagents in the area of fluoroalkylations. Owing to the importance of difluoromethylene (CF2) containing compounds in pharmaceuticals, materials, and agrochemicals, several CF2 group transfer methods using related silicon reagents have been developed and studied in detail. This review summarizes the recent developments and trends in this area. 1 Introduction 2 Trimethyl(trifluoromethyl)silane (Me3SiCF3) 3 (Difluoromethyl)trimethylsilane (Me3SiCF2H) 3.1 Nucleophilic Addition 3.2 Nucleophilic Substitution 3.3 Nucleophilic Difluoromethylation of Electron-Deficient Heterocycles 3.4 Metal-Mediated Cross Coupling 3.5 Oxidative Coupling of Terminal Alkynes 4 Post-functionalizable Difluoromethyl Transfer Reagents 4.1 (Chlorodifluoromethyl)trimethylsilane (Me3SiCF2Cl) 4.2 (Bromodifluoromethyl)trimethylsilane (Me3SiCF2Br) 4.3 [Difluoro(iodo)methyl]trimethylsilane (Me3SiCF2I) 4.4 [Difluoro(phenylthio)methyl]trimethylsilane (Me3SiCF2SPh) 4.5 [Difluoro(phenylsulfonyl)methyl]trimethylsilane (Me3SiCF2SO2Ph) 4.6 Diethyl [Difluoro(trimethylsilyl)methyl]phosphonate [Me3SiCF2P(O)(OEt)2] 4.7 Ethyl Difluoro(trimethylsilyl)acetate (Me3SiCF2CO2Et) 4.8 Difluoro(trimethylsilyl)acetamides (Me3SiCF2CONR2) 4.9 Difluoro(trimethylsilyl)acetonitrile (Me3SiCF2CN) 5 Others 6 Conclusions" @default.
- W2736545116 created "2017-07-31" @default.
- W2736545116 creator A5047158225 @default.
- W2736545116 creator A5079269161 @default.
- W2736545116 date "2017-07-17" @default.
- W2736545116 modified "2023-10-10" @default.
- W2736545116 title "Silicon-Based Reagents for Difluoromethylation and Difluoromethylenation Reactions" @default.
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- W2736545116 doi "https://doi.org/10.1055/s-0036-1588489" @default.
- W2736545116 hasPublicationYear "2017" @default.
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