The installation of fluorine atoms in reactants or catalysts has a dramatic impact on reactivity, regioselectivity and stereoselectivity. Several effects account for the modified stereochemical outcome of reactions with fluorinated versus non-fluorinated molecules. These effects are inherent to the specific properties of fluorine such as the size, the electronegativity, the chelation with metal cations, the hydrogen-bonding ability, the electrostatic and stereoelectronic interactions with neighbouring groups. The use of the effects of fluorine for a desirable goal in asymmetric synthesis is exemplified hereafter
Organofluorine and organometallic chemistry by themselves constitute two potent areas in organic syn...
Even though carbon-fluorine bonds are uncommon in nature, fluorination of organic molecules is well...
The development of new general methods for the synthesis of chiral fluorine-containing molecules is ...
International audienceAll domains of society are impacted by fluorine chemistry. In particular, fluo...
Asymmetric synthesis of fluorine-containing compounds using organocatalysts has been extensively inv...
The chemistry of organic fluorine compounds is a rapidly developing area of research because of thei...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
Fluorinated compounds can exhibit interesting biological properties. The importance of these species...
The number of compounds with fluorine or trifluoromethyl groups present on a stereogenic carbon in p...
The stereoselective incorporation of fluorine atoms into N-heterocycles can lead to dramatic changes...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
One of the most challenging topics in organofluorine chemistry is the asymmetric introduction of flu...
The number of compounds with fluorine or trifluoromethyl groups present on a stereogenic carbon in p...
Even though carbon-fluorine bonds are uncommon in nature, fluorination of organic molecules is well-...
One of the most challenging topics in organofluorine chemistry is the asymmetric introduction of flu...
Organofluorine and organometallic chemistry by themselves constitute two potent areas in organic syn...
Even though carbon-fluorine bonds are uncommon in nature, fluorination of organic molecules is well...
The development of new general methods for the synthesis of chiral fluorine-containing molecules is ...
International audienceAll domains of society are impacted by fluorine chemistry. In particular, fluo...
Asymmetric synthesis of fluorine-containing compounds using organocatalysts has been extensively inv...
The chemistry of organic fluorine compounds is a rapidly developing area of research because of thei...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
Fluorinated compounds can exhibit interesting biological properties. The importance of these species...
The number of compounds with fluorine or trifluoromethyl groups present on a stereogenic carbon in p...
The stereoselective incorporation of fluorine atoms into N-heterocycles can lead to dramatic changes...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
One of the most challenging topics in organofluorine chemistry is the asymmetric introduction of flu...
The number of compounds with fluorine or trifluoromethyl groups present on a stereogenic carbon in p...
Even though carbon-fluorine bonds are uncommon in nature, fluorination of organic molecules is well-...
One of the most challenging topics in organofluorine chemistry is the asymmetric introduction of flu...
Organofluorine and organometallic chemistry by themselves constitute two potent areas in organic syn...
Even though carbon-fluorine bonds are uncommon in nature, fluorination of organic molecules is well...
The development of new general methods for the synthesis of chiral fluorine-containing molecules is ...