The use of a BINOL-derived phosphate as a chiral anionic phase-transfer catalyst in a nonpolar solvent allows the enantioselective fluorination of enamides using Selectfluor as the fluorinating reagent. We demonstrate that a wide range of stable and synthetically versatile α-(fluoro)benzoylimines can be readily accessed with high enantioselectivity. These compounds have the potential to be readily elaborated into a range of highly stereodefined β-fluoroamines, compounds that constitute highly valuable building blocks of particular importance in the synthesis of pharmaceuticals
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...
Ammonium salts are used as phase-transfer catalysts for fluorination with alkali metal fluoride. We ...
The incorporation of fluorine atom into a stereogenic center is a highly challenging transformation ...
The use of a BINOL-derived phosphate as a chiral anionic phase-transfer catalyst in a nonpolar solve...
ABSTRACT: An enantioselective fluorination of allylic alcohols under chiral anion phase-transfer con...
A highly π-facial selective and regioselective fluorination of chiral enamides is described. The rea...
We report a catalytic enantioselective electrophilic fluorination of alkenes to form tertiary and qu...
We report a study involving the successful merger of two separate chiral catalytic cycles: a chiral ...
We report a study involving the successful merger of two separate chiral catalytic cycles: a chiral ...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
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 catalytic asymmetric synthesis of alkyl fluorides, particularly α-fluorocarbonyl compounds, has ...
Potassium fluoride (KF) is an ideal reagent for fluorination because it is safe, easy to handle and ...
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...
Ammonium salts are used as phase-transfer catalysts for fluorination with alkali metal fluoride. We ...
The incorporation of fluorine atom into a stereogenic center is a highly challenging transformation ...
The use of a BINOL-derived phosphate as a chiral anionic phase-transfer catalyst in a nonpolar solve...
ABSTRACT: An enantioselective fluorination of allylic alcohols under chiral anion phase-transfer con...
A highly π-facial selective and regioselective fluorination of chiral enamides is described. The rea...
We report a catalytic enantioselective electrophilic fluorination of alkenes to form tertiary and qu...
We report a study involving the successful merger of two separate chiral catalytic cycles: a chiral ...
We report a study involving the successful merger of two separate chiral catalytic cycles: a chiral ...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
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 catalytic asymmetric synthesis of alkyl fluorides, particularly α-fluorocarbonyl compounds, has ...
Potassium fluoride (KF) is an ideal reagent for fluorination because it is safe, easy to handle and ...
The synthesis of chiral fluorine containing motifs, in particular, chiral fluorine molecules with tw...
Ammonium salts are used as phase-transfer catalysts for fluorination with alkali metal fluoride. We ...
The incorporation of fluorine atom into a stereogenic center is a highly challenging transformation ...