135364-12-4

Upstream product

• 463-49-0 1,2-propanediene 
• 100-51-6 benzyl alcohol 
• 33106-26-2 2-benzyloxypropanol 
• 201230-82-2 carbon monoxide 
• 100-39-0 benzyl bromide 
• 75-56-9 methyloxirane 

Downstream Products

• 6598-36-3 (2-Benzyloxy-propyl)-diethyl-amine 
• 400835-57-6 (2R,3S,4S,5R,6R)-3-(2-Benzyloxy-propoxy)-2-(3,3-diethoxy-propoxy)-6-isobutoxymethyl-4,5-dimethoxy-tetrahydro-pyran 
• 400835-54-3 (2R,3S,4S,5R,6R)-3-(2-Benzyloxy-propoxy)-2-(2,2-dimethoxy-ethoxy)-6-isobutoxymethyl-4,5-dimethoxy-tetrahydro-pyran 
• 135364-14-6 (R,S)-Diethyl-(2-benzyloxypropyl)phosphonat 

Relevant academic research and scientific papers

Regioselective synthesis of halohydrin esters from epoxides: Reaction with acyl halides and rhodium-catalyzed three-component coupling reaction with alkyl halides and carbon monoxide

Regioselective synthesis of halohydrin esters was achieved by (1) the reaction of acyl halides with epoxides and (2) the rhodium-catalyzed three-component coupling reaction of alkyl halides, carbon monoxide, and epoxides. The Royal Society of Chemistry 20

Labelled Representatives of a Possible Intermediate of Fosfomycin Biosythesis in Streptomyces fradiae: Preparation of (R,S)-(2-Hydroxypropyl)-, (R,S)-, (R)-, (S)-(2-Hydroxypropylpropyl- and (R,S)-(2-Hydroxypropyl)phosphonic acid

Racemic methyl O-benzyllactate was reduced to the alcohol, transformed into the bromide and reacted with triethylphosphite to give the diethylphosphonate.Removal of protecting groups afforded a phosphonic acid which was purified as its cyclohexylammonium