02583nam 22006615 450 991042095030332120230822200449.0981-10-3896-110.1007/978-981-10-3896-9(CKB)4100000011435750(DE-He213)978-981-10-3896-9(MiAaPQ)EBC6347279(EXLCZ)99410000001143575020200907d2020 u| 0engurnn#008mamaatxtrdacontentcrdamediacrrdacarrierFluorination /edited by Jinbo Hu, Teruo Umemoto1st ed. 2020.Singapore :Springer Nature Singapore :Imprint: Springer,2020.1 online resource (946 illus., 351 illus. in color. eReference.)Synthetic Organofluorine Chemistry981-10-3895-3 Monofluorination (synthesis of –CF and XF compounds) -- Synthesis of alkyl fluorides -- Synthesis of alkenyl fluorides -- Synthesis of aryl fluorides -- Synthesis of X-F compounds (X = heteroatom) -- Difluorination (synthesies of -CF2- and -CF2H compounds) -- Trifluorination -- Other polyfluorination [synthesies of –CF3, -CmFn (n > 3) and -XFn compounds].This volume reviews the recent advances in formation of C-F bonds and X-F bonds (X = heteroatom) to produce useful fluorinated molecules for pharmaceuticals, materials and more. Reactions and methods associated with fluorination, including monofluorination, difluorination, trifluorination and other polyfluorination that have emerged within the past few years are systematically discussed.Synthetic Organofluorine ChemistryChemistry, OrganicCatalysisPharmaceutical chemistryPolymersMedicinal chemistryOrganic ChemistryCatalysisPharmaceuticsPolymersMedicinal ChemistryChemistry, Organic.Catalysis.Pharmaceutical chemistry.Polymers.Medicinal chemistry.Organic Chemistry.Catalysis.Pharmaceutics.Polymers.Medicinal Chemistry.547Hu JinboUmemoto TeruoMiAaPQMiAaPQMiAaPQBOOK9910420950303321Fluorination1576447UNINA