Using Pd(CF(3)CO(2))(2)/(SS)-f-binaphane as the catalyst, an efficient enantioselective synthesis of cyclic sulfamidates was developed via asymmetric hydrogenation of the corresponding cyclic imines in 2,2,2-trifluoroethanol at room temperature with high enantioselectivities (up to 99% ee)
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate gene...
An enantioselective palladium-catalyzed addition of arylboronic acids to seven-membered cyclic N-sul...
Chiral amines are important synthetic intermediates in the preparation of many physiologically activ...
Using pd(cf(3)co(2))(2)/(S,S)-f-Binaphane as the catalyst, an efficient enantioselective Synthesis o...
Enantioselective Pd-catalyzed hydrogenation of enesulfonamidesAsymmetric hydrogenation of cyclic ene...
Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated ...
The synthesis of cyclic sulfamides by enantioselective Pd‐catalyzed alkene carboamination reactions ...
(Figure Presented) Open for business: The enantio- and diastereoselective nucleophilic ring opening ...
A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)(2)/(S)-SEGPH...
This paper describes the catalytic asymmetric diamination of alkyl dienes using <i>N</i>,<i>N</i>′-d...
Catalytic asymmetric hydrogenation of imines (C=N) is efficient for preparation of chiral amines. Ho...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate gene...
An enantioselective palladium-catalyzed addition of arylboronic acids to seven-membered cyclic N-sul...
Chiral amines are important synthetic intermediates in the preparation of many physiologically activ...
Using pd(cf(3)co(2))(2)/(S,S)-f-Binaphane as the catalyst, an efficient enantioselective Synthesis o...
Enantioselective Pd-catalyzed hydrogenation of enesulfonamidesAsymmetric hydrogenation of cyclic ene...
Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated ...
The synthesis of cyclic sulfamides by enantioselective Pd‐catalyzed alkene carboamination reactions ...
(Figure Presented) Open for business: The enantio- and diastereoselective nucleophilic ring opening ...
A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)(2)/(S)-SEGPH...
This paper describes the catalytic asymmetric diamination of alkyl dienes using <i>N</i>,<i>N</i>′-d...
Catalytic asymmetric hydrogenation of imines (C=N) is efficient for preparation of chiral amines. Ho...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
Dynamic kinetic resolution driven, asymmetric transfer hydrogenation of 4-substituted cyclic sulfami...
An efficient palladium-catalyzed asymmetric hydrogenation via capture of an active intermediate gene...
An enantioselective palladium-catalyzed addition of arylboronic acids to seven-membered cyclic N-sul...
Chiral amines are important synthetic intermediates in the preparation of many physiologically activ...
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