511553-39-2

Upstream product

• 23356-96-9 (S)-1-Pyrrolidin-2-yl-methanol 
• 404868-18-4 2,3-dimethoxyphenyldiphenylphosphine oxide 

Downstream Products

• 848850-67-9 (R)-3-Bromo-1-[2-(diphenyl-phosphinoyl)-6-methoxy-phenyl]-piperidine 
• 848850-86-2 2-{[(S)-1-(2-Diphenylphosphanyl-6-methoxy-phenyl)-pyrrolidin-2-ylmethyl]-ethyl-amino}-ethanol 
• 848850-75-9 2-({(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-ethyl-amino)-ethanol 
• 848850-73-7 4-{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-morpholine 
• 848850-79-3 (R)-1'-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-[1,3']bipiperidinyl 

Relevant academic research and scientific papers

Development of chiral (S)-prolinol-derived ligands for palladium-catalyzed asymmetric allylic alkylation: Effect of a siloxymethyl group on the pyrrolidine backbone

A series of novel chiral aminophosphine ligands are designed and readily prepared from (S)-prolinol. The reactivity and selectivity in the palladium-catalyzed asymmetric allylic alkylation of 1,3-diphenyl-2-propenyl acetate with a dimethyl malonate-BSA-Li

Palladium-catalyzed asymmetric allylic alkylation using chiral prolinol-derived aminophosphine ligands

Palladium-catalyzed asymmetric allylic alkylation of 1,3-diphenyl-2-propenyl acetate (4) with a dimethyl malonate-BSA-LiOAc system has been successfully carried out in the presence of a new chiral prolinol-derived aminophosphine ligand (3e) in good yield