90126-86-6

Upstream product

• 17618-04-1 2,5-di-O-benzyl-D-mannitol 
• 76-83-5 trityl chloride 
• 61490-28-6 1,3:4,6-di-O-benzylidene-D-mannitol 
• 100-39-0 benzyl bromide 
• 114978-02-8 2,5-di-O-benzyl-1,3(R):4,6(R)-di-O-benzylidene-D-mannitol 

Downstream Products

• 322468-17-7 (R)-2-O-benzyl-3-O-tritylglycerol aldehyde 
• 114935-28-3 (R)-2-benzyloxy-3-tert-butyldiphenylsilanyloxy-propan-1-ol 
• 322468-27-9 ((S)-2-O-benzyl-glyceryl)-2-bromoethyl-methylphosphate 
• 322468-25-7 ((R)-2-O-benzyl-glyceryl)-2-bromoethyl-methylphosphate 
• 322468-34-8 (3-O-[2-propyl pentanoyl]-(R)-2-O-benzylglyceryl)-2-bromoethyl-methyl phosphate 
• 322468-29-1 (3-O-[2-(4-isobutlyphenyl propanoyl)]-(R)-2-O-benzylglyceryl)-2-bromoethyl-methyl phosphate 
• 322468-31-5 (3-O-[2-(4-isobutlyphenyl propanoyl)]-(S)-2-O-benzylglyceryl)-2-bromoethyl-methyl phosphate 
• 322468-21-3 ((R)-2-O-benzyl-3-O-tritylglyceryl)-2-bromoethyl-methyl phosphate 
• 322468-23-5 ((S)-2-O-benzyl-3-O-tertbutyldiphenylsilylglyceryl)-2-bromoethyl-methylphosphate 
• 116870-24-7 (3-O-palmitoyl-(R)-2-O-benzylglyceryl)-2-bromoethyl-methyl phosphate 
• 98244-36-1 (S)-2-benzyloxy-1-hexadecyloxy-3-trityloxy-propane 
• 13383-07-8 (S)-2-O-benzyl-3-O-tritylglycerol aldehyde 

Relevant academic research and scientific papers

Drug-phospholipid conjugates as potential prodrugs: Synthesis, characterization, and degradation by pancreatic phospholipase A2

The aim of the present study was the synthesis of phospholipids containing a drug molecule instead of a fatty acid. Valproic acid and ibuprofen served as model compounds. The target molecules were synthesized either starting from sn-glycero-3-phosphocholi