252272-71-2

Upstream product

• 962-39-0 L-Phenylalanine benzyl ester 
• 252272-62-1 (S)-5-(benzyloxymethyl)-3-[2-methoxy-3-(2-naphthylmethoxy)propoxy]-2-methylpyridine-4-carbaldehyde 
• 252272-52-9 (S)-5-(benzyloxymethyl)-3-[2-methoxy-3-(2-naphthylmethoxy)propoxy]-2-methylpyridine-4-carbaldehyde dimethyl acetal 
• 252272-36-9 (S)-1-(t-butyldiphenylsiloxy)-2-methoxy-3-(2-naphthylmethoxy)propane 
• 252272-30-3 (S)-1-(t-butyldiphenylsiloxy)-3-(2-naphthylmethoxy)-2-propanol 
• 252272-47-2 (S)-1-bromo-2-methoxy-3-(2-naphthylmethoxy)propane 
• 252272-41-6 (R)-2-methoxy-3-(2-naphthylmethoxy)-1-propanol 

Downstream Products

• 178457-42-6 benzyl (R)-2-amino-2-methyl-3-phenylpropanoate 

Relevant academic research and scientific papers

Asymmetric α-alkylation of α-amino esters using pyridoxal model compounds with a chiral ionophore function; dependence of stereoselectivity on a chelated metal ion

Asymmetric α-alkylation of α-amino esters by use of novel pyridoxal model compounds having a chiral ionophore function is studied; the stereoselectivity is specifically induced by Na+ and the most effective asymmetric induction occurs with a co