146797-75-3

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 119870-20-1 (R)-(-)-3-tosyloxy-2-benzyloxy-1-propanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 128223-59-6 (R)-1-O-Acetyl-2-O-benzyl-3-tosylglycerol 
• 109429-01-8 (S)-2-(benzyloxy)-3-hydroxypropyl acetate 

Downstream Products

• 147118-43-2 2-((S)-2-Benzyloxy-3-butoxy-propoxy)-tetrahydro-pyran 
• 147118-44-3 (S)-2-O-benzyl-1-O-butyl-3-O-tosylglycerol 
• 147200-16-6 (R)-2-Benzyloxy-3-butoxy-propan-1-ol 
• 146797-77-5 (S)-3-O-hexadecyl-2-O-(4-nitrobenzenesulfonyl)-1-O-tetrahydropyranylglycerol 
• 146923-48-0 (S)-2-O-benzyl-3-O-hexadecyl-1-O-tetrahydropyranylglycerol 

Relevant academic research and scientific papers

New synthesis of 2-thio-PAF and related compounds as substrates of PAF acetylhydrolase and phospholipase A2

2-Thio PAF and related compounds (1 a-c) as substrates of PAF acetylhydrolase and phospholipase A2 were synthesized stereoselectively from optically active 2-O-benzylglycerol monoacetate.

Synthesis of 2-Thio-platlet-activating factor and related compounds

2-Thio-platlet-activating factor and related compounds as substrates of platlet activating factor acetylhydrolase and phospholipase A2 were synthesized from optically active 2-O-benzylglycerol monoacetate.

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