66221-50-9

Upstream product

• 139058-56-3 [(2S,3R)-3-((S)-1-Methoxy-1-phenyl-ethyl)-oxiranyl]-methanol 
• 912646-23-2 (2S,3R,4R,5S)-2,5-dimethoxy-2,5-diphenylhexane-3,4-diol 
• 912646-22-1 (4R,5R)-4,5-bis((S)-1-methoxy-1-phenylethyl)-2,2-dimethyl-1,3-dioxolane 
• 167640-32-6 (αS,α'S,4R,5R)-2,2,α,α'-tetramethyl-α,α'-diphenyl-1,3-dioxolane-4,5-dimethanol 
• 139058-51-8 [(2R,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-oxiranyl]-phenyl-methanone 
• 139058-55-2 (S)-1-[(2R,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-oxiranyl]-1-phenyl-ethanol 

Downstream Products

• 24190-10-1 (S)-(+)-2-methoxy-2-phenylpropionic acid 

Relevant academic research and scientific papers

Asymmetric synthesis of both enantiomers of α-methyl-α-methoxyphenylacetic acid from l-(+)-tartaric acid: formal enantioselective synthesis of insect pheromone (-)-frontalin

Both antipodes of α-methyl-α-methoxyarylacetic acid derivatives were prepared from a common chiralpool precursor l-(+)-tartaric acid. The key step involves the addition of Grignard reagents to 1,4-diketones derived from tartaric acid. The utility of this

A new preparative route to chiral 2,3-epoxy-1,4-butanediols

Chiral 2,3-epoxy-1,4-butanediols including those have a quaternary carbon center have been prepared from optically active 3-cyano-2,3-epoxy-1-propanol.