119835-80-2

Upstream product

• 1074-82-4 potassium phtalimide 
• 23214-66-6 (R)-3-(benzyloxy)-2-hydroxypropyl 4-methylbenzene sulfonate 
• 50-00-0 formaldehyd 
• 119835-79-9 R-(+)-1-benzyloxy-3-phtalimidopropanol 

Downstream Products

• 119835-81-3 R-(+)-5-benzyl-1-<(1'-phtalimidomethyl-2'-benzyloxyethoxy)methyl>-2-oxo-4-methoxypyrimidine 
• 119835-84-6 R-(+)-5-(3'-hydroxybenzyl)-1-<(1'-phtalimidomethyl-2'-hydroxyethoxy)methyl>-2-oxo-4-methoxypyrimidine 
• 119835-82-4 R-(+)-5-benzyl-1-<(1'-phtalimidomethyl-2'-benzyloxyethoxy)methyl>uracil 
• 119835-85-7 R-(+)-5-(3'-benzyloxybenzyl)-1-<(1'-phtalimidomethyl-2'-hydroxyethoxy)methyl>-2-oxo-4-methoxypyrimidine 
• 119835-86-8 R-(+)-5-(3'-benzyloxybenzyl)-1-<(1'-phtalimidomethyl-2'-hydroxyethoxy)methyl>uracil 
• 119835-83-5 R-(+)-5-(3'-benzyloxybenzyl)-1-<(1'-phtalimidomethyl-2'-benzyloxyethoxy)methyl>-2-oxo-4-methoxypyrimidine 

Relevant academic research and scientific papers

Synthesis of enantiomers of 2'-aminomethyl-5-benzylacyclouridine (AM-BAU) and 2'-aminomethyl-5-benzyloxybenzylacyclouridine (AM-BBAU). Potent inhibitors of uridine phosphorylase

Racemic 2'-aminomethyl-5-benzyl-acyclouridine (AM-BAU, 5) and 2'-aminomethyl-5-benzyloxybenzylacyclouridine (AM-BBAU, 6) have been found to be very active inhibitors of uridine phosphorylase [1]. Their enantiomers were synthesized from chiral 2,2-dimethyl