A highly diastereo- and enantioselective silver-catalyzed azomethine ylide–imine (AYI) cycloaddition reaction of glycine aldimino esters with imines was developed in which the Xing-Phos-controlled <i>syn</i>-selective or DTBM-Segphos-induced <i>anti</i>-selective AYI cycloaddition reaction could be applied to the synthesis of a variety of stereodivergent 1-alkyl-2,5-substituted imidazolidines with high yields and excellent enantioselectivities (up to 99% ee) as well as good diastereoselectivities (up to 99:1 dr) under mild reaction conditions
A Ni–Al bimetallic catalyzed enantioselective C–H <i>exo</i>-selective cyclization of imidazoles wit...
Chiral amines bearing a stereocenter in the α position are ubiquitous compounds with many applicatio...
Copper-catalyzed reactions of glycine ester arylimines and methacrylonitrile provide selective acces...
N-Metallated azomethine ylides 5 were generated by the reaction of arylidene glycine imines 1 with A...
A series of chiral ferrocene-based phosphine-phosphoramidite ligands (PPFAPhos) have been employed i...
Catalytic enantioselective 1,3-dipolar cycloaddition between imino esters and electrophilic alkenes,...
The first catalytic asymmetric inverse electron demand 1,3-dipolar cycloaddition of azomethine imine...
Copper-catalyzed reactions of glycine ester arylimines and methacrylonitrile provide selective acces...
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
The diastereoselectively switchable enantioselective Mannich reaction of isatin imines with hydroxya...
1,3-Dipolar cycloadditions of <i>C,N</i>-cyclic azomethine imines with α,β-unsaturated aldehydes can...
Tuning of diastereoselectivity was realized in the Mannich reaction of glycine derivatives with arom...
The reaction of azomethine ylide 1,3-dipoles with olefinic dipo-larophiles forms highly substituted ...
Intensive research over the last few decades in the area of the cycloaddition reactions of metallo-a...
Stereoselective cyclo-addition reactions of azomethine ylides promoted by in situ generated Ag(I)/bi...
A Ni–Al bimetallic catalyzed enantioselective C–H <i>exo</i>-selective cyclization of imidazoles wit...
Chiral amines bearing a stereocenter in the α position are ubiquitous compounds with many applicatio...
Copper-catalyzed reactions of glycine ester arylimines and methacrylonitrile provide selective acces...
N-Metallated azomethine ylides 5 were generated by the reaction of arylidene glycine imines 1 with A...
A series of chiral ferrocene-based phosphine-phosphoramidite ligands (PPFAPhos) have been employed i...
Catalytic enantioselective 1,3-dipolar cycloaddition between imino esters and electrophilic alkenes,...
The first catalytic asymmetric inverse electron demand 1,3-dipolar cycloaddition of azomethine imine...
Copper-catalyzed reactions of glycine ester arylimines and methacrylonitrile provide selective acces...
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
The diastereoselectively switchable enantioselective Mannich reaction of isatin imines with hydroxya...
1,3-Dipolar cycloadditions of <i>C,N</i>-cyclic azomethine imines with α,β-unsaturated aldehydes can...
Tuning of diastereoselectivity was realized in the Mannich reaction of glycine derivatives with arom...
The reaction of azomethine ylide 1,3-dipoles with olefinic dipo-larophiles forms highly substituted ...
Intensive research over the last few decades in the area of the cycloaddition reactions of metallo-a...
Stereoselective cyclo-addition reactions of azomethine ylides promoted by in situ generated Ag(I)/bi...
A Ni–Al bimetallic catalyzed enantioselective C–H <i>exo</i>-selective cyclization of imidazoles wit...
Chiral amines bearing a stereocenter in the α position are ubiquitous compounds with many applicatio...
Copper-catalyzed reactions of glycine ester arylimines and methacrylonitrile provide selective acces...