The development of an efficient and mild synthetic methodology for the construction
of bioactive fluorine-containing molecules represents one of the hot research topics
in general synthetic organic chemistry. In this review, some recent progresses achieved
in the development of detrifluoroacetylatively generated mono-fluorinated enolates via CC
bond cleavage and their asymmetric nucleophilic reactions for assembly of chiral quaternary
C-F center containing compounds.
Use of Ionic Liquids for Synthetic Organic Chemistry
