4201-63-2

Upstream product

• 112-67-4 n-hexadecanoyl chloride 
• 4201-58-5 (2S,3R,4E)-2-(hexadecanoylamido)-4-octadecene-1,3-diol 
• 7143-01-3 Methanesulfonic anhydride 
• 108283-58-5 (2S,3R,4E)-2-azido-3-benzoyl-1-(triphenylmethyl)-4-octadecene-1,3-diol 
• 103348-52-3 C₄₉H₇₈Cl₃NO₁₈ 
• 103348-50-1 (2S,3R,4E)-2-azido-3-benzoyloxy-4-octadecen-1-ol 
• 108283-57-4 (2S,3R,4E)-2-azido-1-(triphenylmethyl)-4-octadecene-1,3-diol 
• 103348-49-8 2-azido-sphingosine 
• 167871-75-2 (2S,3R,4E)-[2',3',6'-tri-O-benzoyl-4'-O-(2'',3'',4'',6''-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-(1'->1)-2-(hexadecanoylamido)-3-O-benzoyl-4-octadecene-1,3-diol 

Relevant academic research and scientific papers

Borinic acid-catalyzed stereo- and site-selective synthesis of β-glycosylceramides

A method for activation of unprotected ceramides towards stereo- and site-selective glycosylation is described. Two-point binding of a diarylborinic acid catalyst to the ceramide accelerates its reactions with 'armed' glycosyl methanesulfonate donors, resulting in the formation of a β-glycosidic linkage at the primary OH group.

Efficient syntheses of a series of glycosphingolipids with 1,2-trans-glycosidic linkages

A series of glycosphingolipids with 1,2-trans-glycosidic linkages were synthesized in the presence of neighboring group participation using trichloroacetimidates as glycosyl donors and an azido-sphingosine as the glycosyl acceptor. During the preparation