691407-72-4

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 18982-54-2 o-bromobenzyl alcohol 
• 691407-89-3 [2'-(tert-butyl-diphenyl-silanyloxymethyl)-biphenyl-3-yl]-methanol 

Downstream Products

• 692736-67-7 (CH₃)2(C₆H₅)4C₅H₂O₄POCH₂C₆H₄C₆H₄CH₂CH(C₃H₃NOC₆H₅)2 
• 691407-76-8 (CH₃)2(C₆H₅)4C₅H₂O₄POCH₂C₆H₄C₆H₄CH₂CH(C₃H₃NOC₆H₅)2 
• 691407-75-7 {3'-[2,2-Bis-((S)-4-phenyl-4,5-dihydro-oxazol-2-yl)-ethyl]-biphenyl-2-yl}-methanol 
• 691407-74-6 {3'-[2,2-Bis-((R)-4-phenyl-4,5-dihydro-oxazol-2-yl)-ethyl]-biphenyl-2-yl}-methanol 
• 691407-90-6 C₄₉H₄₈N₂O₃Si 
• 691407-91-7 C₄₉H₄₈N₂O₃Si 

Relevant academic research and scientific papers

Self-assembled heteroleptic chiral ligands, assymetric catalyst systems and methods

A method of synthesizing a heteroleptic, multiple metal-containing metallocyclic catalyst, particularly suited for asymmetric catalysis, comprising combining a plurality of plural functional group-containing, monodentate ligands of complementary chirality

Asymmetric Catalysis Using Self-Assembled Chiral Bidentate P,P-Ligands

A strategy is described for modular catalyst development based upon metal-directed self-assembly of bifunctional subunits around a structural metal to form a heteroleptic complex in which a second set of ligating groups are now suitably disposed to bind a