The α-fluoroalkyl ketones (3–7) carrying an alkyl, alkenyl, hydroxymethyl, or formyl residue were obtained in enantiomerically pure form by removing, by various methods, the auxiliary sulphinyl group from the α-fluoro α′-sulphinyl ketones (1) and (2) derived from chiral sulphoxides and commercially available α-fluorocarboxylic acids
We are pursuing an approach of asymmetricsynthesis of fluorinated analogues of biologically active c...
International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kociens...
Optically-active sulphenyl or sulphonyl fluorohydrins were obtained by reduction of ketones with bak...
The α-fluoroalkyl ketones (3–7) carrying an alkyl, alkenyl, hydroxymethyl, or formyl residue were ob...
α-Fluoro α′-sulphinyl ketones carrying an α′-alkyl or α′-aryl substituent have been reduced with hig...
The reduction of (Z)-3-fluoro-4-phenyl-1-(p-tolylsulphonyl)but-3-en-2-one with growing cultures of G...
optically pure α′-monofluoro-α-sulphinyl ketones have been reduced with high diastereoselection to g...
Convenient access to homochiral fluoroalkenes is described via a Julia-Kocienski olefination reactio...
Convenient access to homochiral fluoroalkenes is described via a Julia–Kocienski olefination reactio...
optically active sulphenyl and sulphonyl fluorohydrins were obtained by reduction of ketones with ba...
We are pursuing an approach of asymmetricsynthesis of fluorinated analogues of biologically active c...
International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kociens...
Optically-active sulphenyl or sulphonyl fluorohydrins were obtained by reduction of ketones with bak...
The α-fluoroalkyl ketones (3–7) carrying an alkyl, alkenyl, hydroxymethyl, or formyl residue were ob...
α-Fluoro α′-sulphinyl ketones carrying an α′-alkyl or α′-aryl substituent have been reduced with hig...
The reduction of (Z)-3-fluoro-4-phenyl-1-(p-tolylsulphonyl)but-3-en-2-one with growing cultures of G...
optically pure α′-monofluoro-α-sulphinyl ketones have been reduced with high diastereoselection to g...
Convenient access to homochiral fluoroalkenes is described via a Julia-Kocienski olefination reactio...
Convenient access to homochiral fluoroalkenes is described via a Julia–Kocienski olefination reactio...
optically active sulphenyl and sulphonyl fluorohydrins were obtained by reduction of ketones with ba...
We are pursuing an approach of asymmetricsynthesis of fluorinated analogues of biologically active c...
International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kociens...
Optically-active sulphenyl or sulphonyl fluorohydrins were obtained by reduction of ketones with bak...