Homochiral beta-fluorinated gamma,delta-unsaturated carboxylic acids with an allylic fluorinated stereogenic center are available from the corresponding enantiopure allylsilanes. The key step for introduction of the fluorine substituent is an electrophilic fluorodesilylation reaction carried out in the presence of Selectfluor. Reduction of the resulting beta-fluorinated pentenoic acid into the corresponding fluorinated alcohol was also performed leading to the formation of an enantiopure second-generation fluorinated building block
An enantioselective fluorination of allylic alcohols under chiral anion phase-transfer conditions is...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...
Enantiopure N-fluorocinchona alkaloids promoted the electrophilic fluorodesilylation of allyl silane...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
Convenient access to homochiral fluoroalkenes is described via a Julia-Kocienski olefination reactio...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
ABSTRACT: An enantioselective fluorination of allylic alcohols under chiral anion phase-transfer con...
Convenient access to homochiral fluoroalkenes is described via a Julia–Kocienski olefination reactio...
The combination of a practical and highly enantioselective organocatalytic reaction, which allows th...
International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kociens...
Selectively mono-fluorinated sugars have been acknowledged as useful molecular tools for the study o...
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...
Background: Asymmetric introduction of fluorine alpha- to a carbonyl has become popular recently, la...
An enantioselective fluorination of allylic alcohols under chiral anion phase-transfer conditions is...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...
Enantiopure N-fluorocinchona alkaloids promoted the electrophilic fluorodesilylation of allyl silane...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
Convenient access to homochiral fluoroalkenes is described via a Julia-Kocienski olefination reactio...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
Acyclic allylic monofluorides were prepared by electrophilic fluorination of branched (E)-allylsilan...
ABSTRACT: An enantioselective fluorination of allylic alcohols under chiral anion phase-transfer con...
Convenient access to homochiral fluoroalkenes is described via a Julia–Kocienski olefination reactio...
The combination of a practical and highly enantioselective organocatalytic reaction, which allows th...
International audienceConvenient access to homochiral fluoroalkenes is described via a Julia-Kociens...
Selectively mono-fluorinated sugars have been acknowledged as useful molecular tools for the study o...
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...
Background: Asymmetric introduction of fluorine alpha- to a carbonyl has become popular recently, la...
An enantioselective fluorination of allylic alcohols under chiral anion phase-transfer conditions is...
Fluorine is the most electronegative element in the periodic table, and the introduction of one or m...
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...