In this review, recent advances over the past decade in the preparation of fluorinated stereogenic quaternary centers on β-keto esters compounds are analyzed. Since the incorporation of fluorine and fluorinated groups is of special interest in pharmaceutical chemistry, a range of metal-catalyzed and organocatalyzed methods have been developed. Herein, we review the enantioselective fluorination, trifluoromethylation and trifluoromethylthiolation of 3-oxo esters. The scope, the induction of enantioselectivity and mechanistic investigations are presented
The enantioselective synthesis of fluorinated molecules has drawn much attention within the chemical...
International audienceMethods to introduce fluorine atoms or fluoroalkyl groups are highly valuable ...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
In this review, recent advances over the past decade in the preparation of fluorinated stereogenic qu...
Asymmetric synthesis of fluorine-containing compounds using organocatalysts has been extensively inv...
International audienceAll domains of society are impacted by fluorine chemistry. In particular, fluo...
This thesis details the development of a novel catalytic asymmetric route to α-fluorinated ketones. ...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
The chemistry of organic fluorine compounds is a rapidly developing area of research because of thei...
The development of new approaches to the construction of fluorine-containing target molecules is imp...
Due to the unique steric and electronic nature of the fluorine atom, organofluorine compounds have r...
2012-11-20This dissertation is primarily focused on two topics, namely asymmetric nucleophilic fluor...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
A highly enantioselective catalytic method for the synthesis of quaternary α-fluoro derivatives of 3...
One of the most challenging topics in organofluorine chemistry is the asymmetric introduction of flu...
The enantioselective synthesis of fluorinated molecules has drawn much attention within the chemical...
International audienceMethods to introduce fluorine atoms or fluoroalkyl groups are highly valuable ...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
In this review, recent advances over the past decade in the preparation of fluorinated stereogenic qu...
Asymmetric synthesis of fluorine-containing compounds using organocatalysts has been extensively inv...
International audienceAll domains of society are impacted by fluorine chemistry. In particular, fluo...
This thesis details the development of a novel catalytic asymmetric route to α-fluorinated ketones. ...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
The chemistry of organic fluorine compounds is a rapidly developing area of research because of thei...
The development of new approaches to the construction of fluorine-containing target molecules is imp...
Due to the unique steric and electronic nature of the fluorine atom, organofluorine compounds have r...
2012-11-20This dissertation is primarily focused on two topics, namely asymmetric nucleophilic fluor...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
A highly enantioselective catalytic method for the synthesis of quaternary α-fluoro derivatives of 3...
One of the most challenging topics in organofluorine chemistry is the asymmetric introduction of flu...
The enantioselective synthesis of fluorinated molecules has drawn much attention within the chemical...
International audienceMethods to introduce fluorine atoms or fluoroalkyl groups are highly valuable ...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...