International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kocienski olefination reaction. The required homochiral fluorosulfone is synthesized by a Mitsunobu reaction from readily available enantiopure secondary alcohols
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
An unprecedented direct fluorocyclopropanation of allylic alcohols is reported. This simple method i...
International audienceThe selective synthesis of fluoroalkenoates is reported from a pyrimidinyl flu...
International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kociens...
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...
Homochiral beta-fluorinated gamma,delta-unsaturated carboxylic acids with an allylic fluorinated ste...
We are pursuing an approach of asymmetricsynthesis of fluorinated analogues of biologically active c...
Enantiopure N-fluorocinchona alkaloids promoted the electrophilic fluorodesilylation of allyl silane...
The reduction of (Z)-3-fluoro-4-phenyl-1-(p-tolylsulphonyl)but-3-en-2-one with growing cultures of G...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
The combination of a practical and highly enantioselective organocatalytic reaction, which allows th...
α-Fluoro α′-sulphinyl ketones carrying an α′-alkyl or α′-aryl substituent have been reduced with hig...
The α-fluoroalkyl ketones (3–7) carrying an alkyl, alkenyl, hydroxymethyl, or formyl residue were ob...
Organic compounds containing a gem-difluoromethylene group are useful for a variety of applications ...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
An unprecedented direct fluorocyclopropanation of allylic alcohols is reported. This simple method i...
International audienceThe selective synthesis of fluoroalkenoates is reported from a pyrimidinyl flu...
International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kociens...
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...
Homochiral beta-fluorinated gamma,delta-unsaturated carboxylic acids with an allylic fluorinated ste...
We are pursuing an approach of asymmetricsynthesis of fluorinated analogues of biologically active c...
Enantiopure N-fluorocinchona alkaloids promoted the electrophilic fluorodesilylation of allyl silane...
The reduction of (Z)-3-fluoro-4-phenyl-1-(p-tolylsulphonyl)but-3-en-2-one with growing cultures of G...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
The combination of a practical and highly enantioselective organocatalytic reaction, which allows th...
α-Fluoro α′-sulphinyl ketones carrying an α′-alkyl or α′-aryl substituent have been reduced with hig...
The α-fluoroalkyl ketones (3–7) carrying an alkyl, alkenyl, hydroxymethyl, or formyl residue were ob...
Organic compounds containing a gem-difluoromethylene group are useful for a variety of applications ...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
An unprecedented direct fluorocyclopropanation of allylic alcohols is reported. This simple method i...
International audienceThe selective synthesis of fluoroalkenoates is reported from a pyrimidinyl flu...