422321-75-3

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 100-39-0 benzyl bromide 
• 36438-64-9 p-benzyloxystyrene 
• 61439-59-6 2-(4-benzyloxyphenyl)ethanol 
• 40167-10-0 2-[4-(benzyloxy)phenyl]acetaldehyde 
• 4397-53-9 p-benzyloxybenzaldehyde 
• 205587-50-4 (E)-4-(4-benzyloxyphenyl)-2-butenoic acid ethyl ester 

Downstream Products

• 177959-34-1 (2S,3S)-4-(4'-benzyloxyphenyl)-2,3-O-isopropylidenedioxy-1-p-toluenesulfonyloxybutane 
• 422321-77-5 (2S,3S)-4-(4'-benzyloxyphenyl)-2,3-O-isopropylidenedioxybutan-1-ol 
• 177959-36-3 (2S,3S)-4-(4'-benzyloxyphenyl)-1,2-epoxy-3-hydroxybutane 
• 422321-76-4 ethyl (2R,3S)-4-(4'-benzyloxyphenyl)-2,3-O-isopropylidenedioxybutanoate 

Relevant academic research and scientific papers

Asymmetric dihydroxylation and regioselective C-3 indole coupling routes to the anticoccidial antibiotic (+)-diolmycin A2

A highly enantioselective synthesis of (+)-diolmycin A2 starting from 4-hydroxybenzaldehyde and employing the Sharpless asymmetric dihydroxylation and CH3NO2 solvent assisted regioselective C-3 coupling of indole as the key steps is described.