Cinchona alkaloids-derived bifunctional thioureas efficiently catalyse the enantioselective conjugate addition of nitroalkanes to alkylidenemalonates with syn-diastereopreference, opening a route to the synthesis of optically active ?-amino acid derivatives
The asymmetric Michael addition of Meldrum’s acid to nitroalkenes was studied using a novel type of ...
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs...
The enantioselective organocatalytic conjugate addition of a-aminoketone to nitroolefins is reported
Cinchona alkaloids-derived bifunctional thioureas efficiently catalyse the enantioselective conjugat...
The enantioselective conjugate addition of nitromethane to electron-poor alkenes is a powerful synth...
none5siAn easy and simple synthetic approach to optically active alpha,alpha-quaternary alpha-amino ...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
A kind of simple primary amine thiourea organocatalysts was developed. And their application in asym...
International audienceAn unprecedented enantioselective conjugate addition reaction of sodium bisulf...
An efficient bifunctional cinchona alkaloid derived thiourea-promoted enantioselective conjugate add...
An efficient and highly enantioselective Michael addition of nitroalkanes to 3-ylidene oxindoles is ...
Cinchona alkaloid derived primary amine thioureas organo catalyzed Michael addition of nitroalkanes ...
An efficient and highly enantioselective Michael addition of nitroalkanes to 3-ylidene oxindoles is ...
A new class of Michael acceptors based on α,β-unsaturated amino acids has been prepared and applied ...
AbstractEnantio- and Diastereoselective Additions to Nitroalkenes via N-Sulfinyl Urea Organocatalysi...
The asymmetric Michael addition of Meldrum’s acid to nitroalkenes was studied using a novel type of ...
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs...
The enantioselective organocatalytic conjugate addition of a-aminoketone to nitroolefins is reported
Cinchona alkaloids-derived bifunctional thioureas efficiently catalyse the enantioselective conjugat...
The enantioselective conjugate addition of nitromethane to electron-poor alkenes is a powerful synth...
none5siAn easy and simple synthetic approach to optically active alpha,alpha-quaternary alpha-amino ...
A series of new thiourea catalysts prepared from natural amino acids have been applied in organocata...
A kind of simple primary amine thiourea organocatalysts was developed. And their application in asym...
International audienceAn unprecedented enantioselective conjugate addition reaction of sodium bisulf...
An efficient bifunctional cinchona alkaloid derived thiourea-promoted enantioselective conjugate add...
An efficient and highly enantioselective Michael addition of nitroalkanes to 3-ylidene oxindoles is ...
Cinchona alkaloid derived primary amine thioureas organo catalyzed Michael addition of nitroalkanes ...
An efficient and highly enantioselective Michael addition of nitroalkanes to 3-ylidene oxindoles is ...
A new class of Michael acceptors based on α,β-unsaturated amino acids has been prepared and applied ...
AbstractEnantio- and Diastereoselective Additions to Nitroalkenes via N-Sulfinyl Urea Organocatalysi...
The asymmetric Michael addition of Meldrum’s acid to nitroalkenes was studied using a novel type of ...
Highly enantioselective biomimetic Michael addition reactions of malonic acid half thioesters (MAHTs...
The enantioselective organocatalytic conjugate addition of a-aminoketone to nitroolefins is reported