147118-44-3

Upstream product

• 147118-43-2 2-((S)-2-Benzyloxy-3-butoxy-propoxy)-tetrahydro-pyran 
• 119870-20-1 (R)-(-)-3-tosyloxy-2-benzyloxy-1-propanol 
• 147200-16-6 (R)-2-Benzyloxy-3-butoxy-propan-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 146797-75-3 (R)-2-O-benzyl-3-O-tetrahydropyranyl-1-O-tosylglycerol 

Downstream Products

• 147118-50-1 (R)-3-<2-(R)-<(aminocarbonyl)oxy>-3-butoxypropyl>-5-ethyl-5-phenyl-1-propionyloxymethylbarbital 
• 147118-48-7 (S)-3-<2-(R)-<(aminocarbonyl)oxy>-3-butoxypropyl>-5-ethyl-5-phenyl-1-propionyloxymethylbarbital 
• 146727-93-7 (S)-1-O-butyl-3-O-tosylglycerol 

Relevant academic research and scientific papers

Lipase-catalyzed enantioselective synthesis of optically active mephrobarbital, hexobarbital and febarbamate

Chiral 5,5-disubstituted N-acyloxymethylbarbiturates have been obtained in 40-99% optical yields by lipase-catalyzed hydrolyses of 5,5-disubstituted N,N'-bisacyloxymethylbarbiturates in H2O-saturated diisopropyl ether. These chiral barbiturates