The successful design and application of a new type of <i>N</i>-phenyl-imidazole-modified α-heteroatom ketones in asymmetric <i>anti</i>-selective Michael reactions with β-<i>trans</i>-nitroalkenes is reported. High yields and enantioselectivities could be obtained, and the corresponding conjugate adducts could be further transformed into related chiral esters and cyclopropane derivatives with excellent enantioselectivities
The aza-Michael addition reaction is a vital transformation for the synthesis of functionalized chir...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
Organocatalytic asymmetric reactions have proved to be efficient and powerful tools in organic synth...
The successful design and application of a new type of <i>N</i>-phenyl-imidazole-modified α-heteroat...
Michael addition is an important reaction because it can be used to synthesize a wide range of natur...
Michael addition is one of the most important carbon–carbon bond formation reactions. In this study,...
International audienceDespite tremendous efforts towards the development of organocatalytic enantios...
A <i>tert</i>-leucine-derived chiral diamine catalyzes the asymmetric Michael addition of nitrometha...
Azaarenes are of widespread chemical significance, being present in numerous chiral, biologically a...
The asymmetric organocatalyzed Michael addition of aldehydes to alpha,beta-gamma,delta-unsaturated n...
A novel bifunctional organocatalytic Michael addition of a succinimide-derived pronucleophile to nit...
International audienceThe first organocatalytic enantio- and diastereoselective conjugate addition o...
Primary amine-guanidines derived from trans-cyclohexane-1,2-diamines are used as organocatalysts for...
Herein, an asymmetric organocatalytic aza-Michael addition reaction of ketimines to nitroolefins is ...
The first asymmetric synthesis of 1,3-dinitro compounds through Michael addition of nitroalkanes to ...
The aza-Michael addition reaction is a vital transformation for the synthesis of functionalized chir...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
Organocatalytic asymmetric reactions have proved to be efficient and powerful tools in organic synth...
The successful design and application of a new type of <i>N</i>-phenyl-imidazole-modified α-heteroat...
Michael addition is an important reaction because it can be used to synthesize a wide range of natur...
Michael addition is one of the most important carbon–carbon bond formation reactions. In this study,...
International audienceDespite tremendous efforts towards the development of organocatalytic enantios...
A <i>tert</i>-leucine-derived chiral diamine catalyzes the asymmetric Michael addition of nitrometha...
Azaarenes are of widespread chemical significance, being present in numerous chiral, biologically a...
The asymmetric organocatalyzed Michael addition of aldehydes to alpha,beta-gamma,delta-unsaturated n...
A novel bifunctional organocatalytic Michael addition of a succinimide-derived pronucleophile to nit...
International audienceThe first organocatalytic enantio- and diastereoselective conjugate addition o...
Primary amine-guanidines derived from trans-cyclohexane-1,2-diamines are used as organocatalysts for...
Herein, an asymmetric organocatalytic aza-Michael addition reaction of ketimines to nitroolefins is ...
The first asymmetric synthesis of 1,3-dinitro compounds through Michael addition of nitroalkanes to ...
The aza-Michael addition reaction is a vital transformation for the synthesis of functionalized chir...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
Organocatalytic asymmetric reactions have proved to be efficient and powerful tools in organic synth...