96363-22-3

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 96363-20-1 D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoic acid 
• 96363-21-2 methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate 

Downstream Products

• 96363-23-4 (1S)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propanol 
• 96363-23-4 (1R)-D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)<1-2H>propanol 

Relevant academic research and scientific papers

Synthesis of (4R)-D,L-- and (4S)-D,L-Homoserine Lactones

The (4R)-D,L-- and (4S)-D,L-homoserine lactone hydrochloride salts were prepared from D,L-3-amino-3-(4-methoxyphenyl)propanoic acid (1) in eight steps in an overall yields of 5.0percent.Amino acid 1 was converted into D,L-3-(1,1-dimethyletho

PREPARATION OF 1-DEUTERIOALDEHYDES VIA THE USE OF DIISOBUTYLALUMINUM DEUTERIDE (DIBAL-D)

Deuterioaldehydes, essential precursors in the preparation of chiral primary deuterioalcohols, have been prepared in yields ranging from 55-75percent via reduction of methyl and ethyl esters at -78 oC with diisobutylaluminum deuteride (DIBAL-D).The stoich