600738-29-2

Upstream product

• 199393-31-2 (R)-2-(tert-butoxycarbonyl)amino-2-(4-benzyloxyphenyl)ethanol 
• 600738-27-0 N₁,N₃-di{(1R)-1-[4-(benzyloxy)phenyl]-2-hydroxyethyl}-2,2-diethylmanonamide 
• 289051-79-2 (R)-2-hyrdoxy-1-(4-benzyloxyphenyl)ethylamine 
• 54505-72-5 diethylmalonyl chloride 
• 69489-40-3 D-2-[p-(benzyloxy)phenyl]glycine 
• 22818-40-2 D-4-hydroxyphenylglycine 
• 100-39-0 benzyl bromide 
• 127526-64-1 (R)-(4-benzyloxyphenyl)(tert-butoxycarbonylamino)acetic acid 

Downstream Products

• 468732-53-8 2,2'-(1-ethylpropylidene)bis[(4R)-4-(4-benzyloxy)phenyl-4,5-dihydro-1,3-oxazole] 

Relevant academic research and scientific papers

Syntheses of amino alcohols and chiral C2-symmetric bisoxazolines derived from O-alkylated R-4-hydroxyphenylglycine and S-tyrosine

Chiral C2-symmetric bisoxazolines 1b-f and 2b,c, derived from 4′-O-alkylated R-4-hydroxyphenylglycine or S-tyrosine, were prepared. As intermediates, a series of chiral amino alcohols possessing substituted phenolic groups was prepared and fully characterized.