908003-49-6

Upstream product

• 163493-02-5 (R)-2-(N,N-dibenzylamino)-3-O-benzyl-1,3-propanediol 
• 100-39-0 benzyl bromide 
• 58577-87-0 O-benzyl-L-serinol 

Relevant academic research and scientific papers

Highly enantioselective synthesis of β-amino alcohols: A catalytic version

(Chemical Equation Presented) Highly enantioselective rearrangement of β-amino alcohols was realized by using a catalytic amount of trifluoroacetic anhydride.

Stereospecific rearrangement of β-amino alcohols catalyzed by H 2SO4

Highly enantioselective rearrangement of β-amino alcohols was realized by using a catalytic amount of H2SO4. Georg Thieme Verlag Stuttgart.

Highly enantioselective synthesis of β-amino alcohols

N,N-Dialkyl-β-amino alcohols derived from α-amino acids can be rearranged enantiospecifically by using TFAA/Et3N/NaOH to give 1,2-amino alcohols with enantiomeric excess up to 99%.