Solvent- and Catalyst-Free Synthesis of gem -Difluorinated and Polyfluoroarylated Compounds with Nucleophilic or Electrophilic Fluorine-Containing Reaction Partners, Respectively.
Lingheng LiJinshan LiPublished in: Molecules (Basel, Switzerland) (2024)
A novel, efficient and environmentally friendly solvent-free and catalyst-free approach for the synthesis of structurally diverse gem -difluorinated and polyfluoroarylated derivatives with readily available nucleophilic and electrophilic fluorine-containing reaction partners, difluoroenoxysilane and pentafluorobenzaldehyde, is described. This neat protocol is induced by the direct hydrogen-bond interactions between fluorinated and non-fluorinated reactants without the use of heavy metal catalysts or volatile organic solvents and with no need for column chromatographic separation for most cases.
Keyphrases
- ionic liquid
- heavy metals
- highly efficient
- room temperature
- positron emission tomography
- metal organic framework
- randomized controlled trial
- liquid chromatography
- reduced graphene oxide
- pet imaging
- risk assessment
- computed tomography
- carbon dioxide
- mass spectrometry
- high resolution
- gas chromatography
- hepatitis c virus
- solid phase extraction
- structure activity relationship