210993-14-9

Upstream product

• 1027270-14-9 C₂₆H₄₀N₂O₂Si₂ 
• 492-41-1 (1R,2S)-norephedrine 
• 106-93-4 ethylene dibromide 
• 151528-61-9 (1S,2R)-N,N'-bis-<(2-hydroxy-1-methyl-2-phenyl)ethyl>oxamide 

Downstream Products

• 226215-76-5 (5R,4S,2S,5'S,4'S,2'S)-N,N'-ethylene(5,5'-diphenyl-4,4',2,2'-tetramethyl)-2,2'-bisoxazolidine 
• 1108617-17-9 (-)-1,3-bis[(1S,2R)-2-hydroxy-1-methyl-2-phenylethyl]imidazolinium iodide 
• 1108617-16-8 (-)-1,3-bis[(1S,2R)-2-hydroxy-1-methyl-2-phenylethyl]imidazolinium bromide 
• 136021-21-1 1,4-bis<(1'S,2'R)-(2'-hydroxy-1'-methyl-2'-phenyl)>ethylpiperazine 
• 226215-77-6 (2R,4S,5R,17S,19S,20R)-N,N'-ethylene(2,4,19-trimethyl-5,17,20-triphenyl)-2,17-bisoxazolidine 
• 226215-74-3 (4S,5R,2S,4'S,5'R,2'S)-N,N'-ethylene(4,4'-dimethyl-5,5'-diphenyl)-2,2'-bisoxazolidine 

Relevant academic research and scientific papers

Asymmetric nanocatalysis: N-heterocyclic carbenes as chiral modifiers of Fe3O4/Pd nanoparticles

Superficial success: A chiral N-heterocyclic carbene (NHC *) is used to modify Fe3O4/Pd nanoparticles, which then catalyze asymmetric α-arylations. This successful synthesis of a heterogeneous catalyst and its appliation i

New enantiopure imidazolinium carbene ligands incorporating two hydroxy groups for Lewis acid-catalyzed diethyl zinc addition to aldehydes

New enantiopure imidazolinium carbene ligands incorporating two hydroxy functions have been synthesized from commercially available chiral amino alcohols and diamines. These ligands in combination with different metallic salts have been investigated in th

A convenient preparation of (1R,2S,7S,8R)-3,5-diaza-2,7-dimethyl-1,8- diphenyloctan-1,8-diol and its enantiomer

The synthesis of (1R,2S,7S,8R)-3,5-diaza-2,7-dimethyl-1,8-diphenyloctan-1, 8-diol 6 and its enantiomer 7 are described utilising (-)-(1R,2S)- or (+)-(1S,2R)-norephedrine, respectively.

A new method for the preparation of unsymmetrical 1,4-substituted piperazine derivatives

Symmetrical and unsymmetrical N,N'-piperazine derivatives of (-)- norephedrine and o-aminophenol were synthesized stereoselectively in yields >70% by reduction of the corresponding N,N'-ethylenebisoxazolidine heterocycles. The stereochemistry at the ring fusion carbons was established by NMR spectroscopy and X-ray crystallography.

Amino alcohol coordination in ruthenium(II)-catalysed asymmetric transfer hydrogenation of ketones

The nature of ruthenium-amino alcohol precursors in the catalytic cycle of asymmetric hydrogen transfer reactions was studied using two C2- symmetrical tetradentate ligands (1 and 2) that were synthesised from (nor)ephedrine. The structure of t