Design and Synthesis of Optically Active Trans-Chelating Diphosphine Ligands. Application for Catalytic Asymmetric Synthesis
Author:
Affiliation:
1. a Department of Synthetic Chemistry and Biological Chemistry , Kyoto University , Kyoto 606–8501, Japan
2. b Department of Synthetic Chemistry and Biological Chemistry , Kyoto University , Kyoto 606–8501, Japan
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426509908546283
Reference4 articles.
1. Trans-Chelating Chiral Peralkyldiphosphine Ligands (R,R)-(S,S)-2,2″-Bis[1-(dialkylphosphino)ethyl]-1,1″-biferrocenes (AlkylTRAPs) and Their Transition Metal Complexes
2. Synthesis and Structures of Trans-Chelating Chiral Diphosphine Ligands Bearing Aromatic P-Substituents, (S,S)-(R,R)- and (R,R)-(S,S)-2,2''-Bis[1-(diarylphosphino)ethyl]-1,1''-biferrocene (ArylTRAPs) and Their Transition Metal Complexes
3. Catalytic asymmetric synthesis with trans-chelating chiral diphosphine ligand TRAP: rhodium-catalyzed asymmetric Michael addition of .alpha.-cyano carboxylates
4. Enantioselective hydrogenation of .beta.-disubstituted .alpha.-acetamidoacrylates catalyzed by rhodium complexes with TRAP trans-chelating chiral phosphine ligands.
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