98244-36-1

Upstream product

• 96093-53-7 (S)-3-(1-hexadecyloxy)-1-(trityloxy)propan-2-ol 
• 100-39-0 benzyl bromide 
• 13383-07-8 (S)-2-O-benzyl-3-O-tritylglycerol aldehyde 
• 112-82-3 hexadecanyl bromide 
• 36653-82-4 1-Hexadecanol 
• 17618-04-1 2,5-di-O-benzyl-D-mannitol 
• 90126-86-6 2,5-di-O-benzyl-1,6-di-O-trityl-D-mannitol 
• 114978-02-8 2,5-di-O-benzyl-1,3(R):4,6(R)-di-O-benzylidene-D-mannitol 
• 76-83-5 trityl chloride 
• 20779-14-0 methanesulfonic acid hexadecyl ester 
• 100-44-7 benzyl chloride 

Downstream Products

• 84415-90-7 (R)-2-benzyloxy-3-hexadecyloxy-propan-1-ol 
• 96022-71-8 2-O-Benzyl-3-O-hexadecyl-1-O-<2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranosyl>-sn-glycerin 
• 96998-53-7 3-O-hexadecyl-2-O-benzyl-sn-glycero-1-phosphocholine 
• 90130-75-9 3-O-hexadecyl-2-lyso-sn-glycero-1-phosphocholine 

Relevant academic research and scientific papers

Stereoselective Synthesis of Long-chain 1-O-(β-D-Maltosyl)-3-O-alkyl-sn-glycerols (Alkyl Glyceryl Ether Lysoglycolipids)

The synthesis of long-chain 2-O-benzyl-3-O-alkyl-sn-glycerols 5 was improved, making these compounds easily accessible for glycosylation experiments.Glycosylation with α-acetobromomaltose following a modified Koenings-Knorr procedure after removal of the protective groups yielded the title compound 9 in good yields.These compounds represent examples of alkyl glyceryl ether lysoglycolipids.Some properties of these amphiphilic compounds with a nonionic carbohydrate head-group differ not much (critical micell concentration, hemolytic activity), other properties differ very much (antitumor efficiency) from the properties of the analogous compounds with a zwitterionic phosphorylcholine head-group.