352219-99-9

Upstream product

• 352219-98-8 (3R,4S,5R)-3,4-O-isopropylidene-1-tert-butyldiphenylsilyloxy-2,6-dioxotricosan-5-yl acetate 
• 352219-97-7 (3R,4R,5S,6R)-2-heptadecyl-tetrahydro-2-hydroxy-4,5-O-isopropylidene-6-tert-butyldiphenylsilyloxy-methyl-2H-pyran-3-yl acetate 
• 352219-96-6 (3R,4R,5S,6R)-2-heptadecyl-tetrahydro-4,5-O-isopropylidene-6-tert-butyldiphenylsilyloxy-methyl-2H-pyran-2,3-diol 
• 224324-95-2 tert-butyl-(6-heptadecyl-2,2-dimethyl-3a,7a-dihydro-4H-[1,3]dioxolo[4,5-c]pyran-4-ylmethoxy)-diphenyl-silane 
• 57-11-4 stearic acid 

Relevant academic research and scientific papers

C-Glycoside analogues of β-galactosylceramide with a simple ceramide substitute: Synthesis and binding to HIV-1 gp120

The synthesis and HIV-1 gp120 binding of C- and aza-C-glycoside analogues of β-galactosylceramide (GalCer) that contain a simple C-17 hydrocarbon chain as a ceramide substitute are described. Both compounds originate from stearic acid, and a carbohydrate-

Synthesis of aza-C-galacto disaccharides from C1-substituted galactals

C1-substituted galactals are transformed via the double reductive amination on their 1,5-diketone derivatives, to aza-β-C-galacto-disaccharides.