208184-51-4

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 88099-67-6 methyl (2S)-2-(dibenzylamino)-3-hydroxypropanoate 
• 352530-50-8 methyl (S)-3-(tert-butyldimethylsilyloxy)-2-(dibenzylamino)propanoate 
• 239437-14-0 N,N-dibenzyl-O-tert-butyldimethylsilyl serinol 
• 925-90-6 ethylmagnesium bromide 
• 125654-82-2 (S)-3-(tert-Butyl-dimethyl-silanyloxy)-2-dibenzylamino-propionaldehyde 

Downstream Products

• 208184-60-5 (3R,5R)-4-Dibenzylamino-heptane-3,5-diol 
• 208184-54-7 (2R,3R)-2-Dibenzylamino-3-(2-methoxy-ethoxymethoxy)-pentanal 
• 208184-53-6 (2S,3R)-2-Dibenzylamino-3-(2-methoxy-ethoxymethoxy)-pentan-1-ol 
• 208184-52-5 Dibenzyl-[(1S,2R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-(2-methoxy-ethoxymethoxy)-butyl]-amine 

Relevant academic research and scientific papers

Stereodivergent synthesis of all diastereomers of 4-aminoheptane-3,5- diol from (L)-serine

The synthesis of the two diasteromeric meso forms of 4-amino-3,5- heptanediol (3R,4r,5S)-1a and (35,4s,5R)-1b and the two pseudo C2-symmetric enantiomers (3S,5S)-1c and (3R,5R)-ent-1c is described by stereocontrolled ethylmagnesium bromide or d