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Fluorination Reagents [Synthetic Reagents]
Introduction of fluorine into a certain position of bioactive compound such as a pharmaceutical and an agricultural chemical may remarkably reduce the toxicity of the compound, or improve the efficiency of medicine. This is due to the mimic and blocking effect characterized by fluorine. Many compounds, such as 5-fluorouracil, have been reported as success case. Attempts to efficiently synthesize fluorine-containing compounds are performed in many fields. Methods to introduce fluorine into a certain position through the use of fluorinating agents have been reported.
Fluorine, difluoromethyl group, trifluoromethyl group, trifluoromethlythio group and etc. are known as below. This page shows fluorinating agents categorized by functional group insertion.
Topics and Information on Fluorination
References
- Substituted phenylsulfur trifluoride and other like fluorinating agents
- T. Umemoto, Y. Xu, U.S. Patent 7265247, 2007.
- T. Umemoto, R. P. Singh, U.S. Patent 7381846, 2008.
- Triethyl 2-Fluoro-2-phosphonoacetate
- Synthesis and properties of 12-fluororetinal and 12-fluororhodopsin. Model system for fluorine-19 NMR studies of visual pigments
- Fluorinated retinoic acids and their analogs. 3. Synthesis and biological activity of aromatic 6-fluoro analogs
- Synthesis of dienic fluorinated analogs of insect sex pheromones
- 2-Diethoxyphosphoryl alcanoic acid dianions (lithium α-lithiocarboxylates): IV. A direct route to 2-fluoro-2-alkenoic acids by the Horner synthesis. Application in the field of pyrethroids
- Fluorinated Johnson Reagent for Transfer-Trifluoromethylation to Carbon Nucleophiles
New Stable Nucleophilic Fluorinating Reagent (FLUOLEAD)Trifluoromethylating ReagentsDifluorocarbene PrecursorsTrifluoromethylthiolation Reagents3,3,3-Trifluoropropenylation Reagent: Ikeda-Omote ReagentSulfinate Salt for Trifluoromethylation via C-H Bond ActivationUnique Fluorinating Reagent with Various ReactivitiesTrifluoromethylating Reagents Used in Nucleophilic ReactionsCopper Complexes for Trifluoromethylation via Oxidative Cross-couplingDeoxyfluorination Reagents by the Ritter GroupStable Hydrogen Fluoride (HF) Complex for Nucleophilic Fluorination: DMPU-HFDifluoromethylation Reagents, Difluoromethylenation ReagentsMorpholine Derivative Usable for TrifluoromethylationHypervalent Iodine Reagentfor Photoredox TrifluoromethylationSulfonium Salt for Photo-catalytic DifluoromethylationSulfonium Salt for Both Trifluoromethylation and MesitylationPowerful, Electrophilic Trifluoromethylating Agent: Umemoto Reagent IVEasy-to-handle and Mild Electrophilic Fluorinating Agent: NFBBSafe and Easy-to-handle Trifluoromethoxylating Agent: TFNfHighly Versatile and Atom-Efficient Trifluoromethylthiolating Agent: TTSTFluorination Reagents, Fluorinated Building BlocksEasy-to-Handle Trifluoromethylating Agent for Multiple UsesCyanodifluoromethylation Reagent: TMSCF2CNEfficient, Easy-to-Handle, and Environmentally Benign Difluoromethylating AgentReagent for the Introduction of Fluorine‑Containing Groups such as gem-Fluorovinyl Group