Pd/bisphosphines complexes are highly effective catalysts for asymmetric hydrogenation of activated imines in trifluoroethanol. The asymmetric hydrogenation of N-diphenylphosphinyl ketimines 3 with Pd(CF3CO2)/(S)-SegPhos indicated 87-99% ee, and N-tosylimines 5 could gave 88-97% ee with Pd(CF3CO2)/(S)-SynPhos as a catalyst. Cyclic N-sulfonylimines 7 and 11 were hydrogenated to afford the useful chiral sultam derivatives in 79-93% ee, which are important organic synthetic intermediates and structural units of agricultural and pharmaceutical agents
Asymmetric hydrogenation of C=C bonds is of the highest importance in organic synthesis, and such re...
A series of chiral spiroketal bisphosphine ligands containing 1,1′-spirobi(3H,3′H)isobenzofuran ba...
A series of chiral spiroketal bisphosphine ligands containing 1,1′-spirobi(3H,3′H)isobenzofuran ba...
A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)(2)/(S)-SEGPH...
Using pd(cf(3)co(2))(2)/(S,S)-f-Binaphane as the catalyst, an efficient enantioselective Synthesis o...
Catalytic asymmetric hydrogenation of imines (C=N) is efficient for preparation of chiral amines. Ho...
Enantioselective Pd-catalyzed hydrogenation of enesulfonamidesAsymmetric hydrogenation of cyclic ene...
Using Pd(CF(3)CO(2))(2)/(SS)-f-binaphane as the catalyst, an efficient enantioselective synthesis of...
Catalytic asymmetric hydrogenations of prochiral unsaturated compounds, such as olefins, ketones, an...
The research described in this thesis is directed toward the efficient, enantioselective synthesis o...
Abstract: A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)2/(...
Chiral amines are important synthetic intermediates in the preparation of many physiologically activ...
A little goes a long way: A 1 mol % loading of the chiral phosphoric acid catalyst 2 converts aromat...
Chiral molecules exist in two different forms called enantiomers, which are non-superimposable mirro...
Asymmetric hydrogenation of C=C bonds is of the highest importance in organic synthesis, and such re...
Asymmetric hydrogenation of C=C bonds is of the highest importance in organic synthesis, and such re...
A series of chiral spiroketal bisphosphine ligands containing 1,1′-spirobi(3H,3′H)isobenzofuran ba...
A series of chiral spiroketal bisphosphine ligands containing 1,1′-spirobi(3H,3′H)isobenzofuran ba...
A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)(2)/(S)-SEGPH...
Using pd(cf(3)co(2))(2)/(S,S)-f-Binaphane as the catalyst, an efficient enantioselective Synthesis o...
Catalytic asymmetric hydrogenation of imines (C=N) is efficient for preparation of chiral amines. Ho...
Enantioselective Pd-catalyzed hydrogenation of enesulfonamidesAsymmetric hydrogenation of cyclic ene...
Using Pd(CF(3)CO(2))(2)/(SS)-f-binaphane as the catalyst, an efficient enantioselective synthesis of...
Catalytic asymmetric hydrogenations of prochiral unsaturated compounds, such as olefins, ketones, an...
The research described in this thesis is directed toward the efficient, enantioselective synthesis o...
Abstract: A variety of substituted N-diphenylphosphinyl imines were hydrogenated using Pd(CF3CO2)2/(...
Chiral amines are important synthetic intermediates in the preparation of many physiologically activ...
A little goes a long way: A 1 mol % loading of the chiral phosphoric acid catalyst 2 converts aromat...
Chiral molecules exist in two different forms called enantiomers, which are non-superimposable mirro...
Asymmetric hydrogenation of C=C bonds is of the highest importance in organic synthesis, and such re...
Asymmetric hydrogenation of C=C bonds is of the highest importance in organic synthesis, and such re...
A series of chiral spiroketal bisphosphine ligands containing 1,1′-spirobi(3H,3′H)isobenzofuran ba...
A series of chiral spiroketal bisphosphine ligands containing 1,1′-spirobi(3H,3′H)isobenzofuran ba...