Enantioselective organocatalytic conjugate addition of fluorocarbon nucleophiles to α,β-unsaturated aldehydes
Highly chemo- and enantioselective organocatalytic conjugate additions of fluorocarbon nucleophiles to a,b-unsaturated aldehydes and the construction of a quaternary carbon stereocenter bearing a fluorine atom with high enantioselectivity was reported. Af
Catalytic enantioselective conjugate addition of fluorobis(phenylsulfonyl) methane to enals: Synthesis of chiral monofluoromethyl compounds
A new highly catalytic enantioselective Michael addition of fluorobis(phenylsulfonyl)methane to α,β-unsaturated aldehydes has been developed for the preparation of chiral monofluoromethyl compounds under mild reaction conditions.