A new enantioselective desymmetrizing Mizoroki–Heck reaction is reported. The process affords high yields and enantioselectivities of tricyclic structures containing all-carbon quaternary stereocenters. The substrates for the reaction are efficiently synthesized from Birch reduction–alkylation of benzoic acid and benzoate esters
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
An efficient synthetic method for establishing chiral α-thio-α-quaternary stereogenic center was suc...
The enantioselective conjugate alkynylation of β-aryl-β-trifluoromethyl enones has been carried out ...
A new enantioselective desymmetrizing Mizoroki–Heck reaction is reported. The process affords high y...
Novel phenanthridinone analogues with an all-carbon quaternary stereocenter have been enantioselecti...
The Birch reduction – alkylation is an effective way to form all-carbon quaternary centers from inex...
Quaternary carbon stereocentres-carbon atoms to which four distinct carbon substituents are attached...
A catalytic enantioselective synthesis of α-arylaminocyclobutanones from racemic α-hydroxycyclobutan...
Enantiopure carbonyl compounds bearing tetrasubstituted α-stereogenic centers are versatile building...
A highly enantioselective Friedel–Crafts alkylation reaction of indoles with β-CF<sub>3</sub>-β-disu...
An organocatalytic enantioselective synthesis of α-(benzylamino)cyclobutanones has been achieved by ...
Highly enantioselective catalytic asymmetric reactions of rationally designed α-alkylidene β-keto im...
An enantioselective desymmetric aryl C–O coupling reaction was demonstrated under the catalysis of C...
A <i>tert</i>-leucine-derived chiral diamine catalyzes the asymmetric Michael addition of nitrometha...
A tandem Michael–Henry reaction of 2-mercaptoquinoline-3-carbaldehydes with nitroolefins using hydr...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
An efficient synthetic method for establishing chiral α-thio-α-quaternary stereogenic center was suc...
The enantioselective conjugate alkynylation of β-aryl-β-trifluoromethyl enones has been carried out ...
A new enantioselective desymmetrizing Mizoroki–Heck reaction is reported. The process affords high y...
Novel phenanthridinone analogues with an all-carbon quaternary stereocenter have been enantioselecti...
The Birch reduction – alkylation is an effective way to form all-carbon quaternary centers from inex...
Quaternary carbon stereocentres-carbon atoms to which four distinct carbon substituents are attached...
A catalytic enantioselective synthesis of α-arylaminocyclobutanones from racemic α-hydroxycyclobutan...
Enantiopure carbonyl compounds bearing tetrasubstituted α-stereogenic centers are versatile building...
A highly enantioselective Friedel–Crafts alkylation reaction of indoles with β-CF<sub>3</sub>-β-disu...
An organocatalytic enantioselective synthesis of α-(benzylamino)cyclobutanones has been achieved by ...
Highly enantioselective catalytic asymmetric reactions of rationally designed α-alkylidene β-keto im...
An enantioselective desymmetric aryl C–O coupling reaction was demonstrated under the catalysis of C...
A <i>tert</i>-leucine-derived chiral diamine catalyzes the asymmetric Michael addition of nitrometha...
A tandem Michael–Henry reaction of 2-mercaptoquinoline-3-carbaldehydes with nitroolefins using hydr...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
An efficient synthetic method for establishing chiral α-thio-α-quaternary stereogenic center was suc...
The enantioselective conjugate alkynylation of β-aryl-β-trifluoromethyl enones has been carried out ...