Using pd(cf(3)co(2))(2)/(S,S)-f-Binaphane as the catalyst, an efficient enantioselective Synthesis of sultams was developed via asymmetric hydrogenation of the corresponding cyclic imines with high enantioselectivities. The hydrogenation products can be conveniently transformed to chiral homoallylic amines without loss of enantioselectivity
The transition metal catalyzed asymmetric hydrogenation of unsaturated compounds arguably presents o...
A novel palladium-catalyzed intramolecular reductive amination of ketones with weakly nucleophilic s...
Catalytic asymmetric hydrogenations of prochiral unsaturated compounds, such as olefins, ketones, an...
Using Pd(CF(3)CO(2))(2)/(SS)-f-binaphane as the catalyst, an efficient enantioselective synthesis of...
Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated ...
Enantioselective Pd-catalyzed hydrogenation of enesulfonamidesAsymmetric hydrogenation of cyclic ene...
A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)(2)/(S)-SEGPH...
Catalytic asymmetric hydrogenation of imines (C=N) is efficient for preparation of chiral amines. Ho...
Highly enantioselective palladium-catalyzed formal hydrogenolysis of racemic N-sulfonyloxaziridines ...
Chiral amines are important synthetic intermediates in the preparation of many physiologically activ...
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate gene...
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate gene...
The synthesis of cyclic sulfamides by enantioselective Pd‐catalyzed alkene carboamination reactions ...
Palladium-Catalyzed Asymmetric Hydrogenation of Simple Ketimines Using a Bronsted Acid as ActivatorU...
A palladium-catalyzed intramolecular asymmetric reductive amination of racemic -branched ketones bea...
The transition metal catalyzed asymmetric hydrogenation of unsaturated compounds arguably presents o...
A novel palladium-catalyzed intramolecular reductive amination of ketones with weakly nucleophilic s...
Catalytic asymmetric hydrogenations of prochiral unsaturated compounds, such as olefins, ketones, an...
Using Pd(CF(3)CO(2))(2)/(SS)-f-binaphane as the catalyst, an efficient enantioselective synthesis of...
Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated ...
Enantioselective Pd-catalyzed hydrogenation of enesulfonamidesAsymmetric hydrogenation of cyclic ene...
A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)(2)/(S)-SEGPH...
Catalytic asymmetric hydrogenation of imines (C=N) is efficient for preparation of chiral amines. Ho...
Highly enantioselective palladium-catalyzed formal hydrogenolysis of racemic N-sulfonyloxaziridines ...
Chiral amines are important synthetic intermediates in the preparation of many physiologically activ...
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate gene...
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate gene...
The synthesis of cyclic sulfamides by enantioselective Pd‐catalyzed alkene carboamination reactions ...
Palladium-Catalyzed Asymmetric Hydrogenation of Simple Ketimines Using a Bronsted Acid as ActivatorU...
A palladium-catalyzed intramolecular asymmetric reductive amination of racemic -branched ketones bea...
The transition metal catalyzed asymmetric hydrogenation of unsaturated compounds arguably presents o...
A novel palladium-catalyzed intramolecular reductive amination of ketones with weakly nucleophilic s...
Catalytic asymmetric hydrogenations of prochiral unsaturated compounds, such as olefins, ketones, an...