138223-67-3

Upstream product

• 81577-69-7 [2R,4R,5R]-5-hydroxy-2-phenyl-[1,3]dioxane-4-carbaldehyde 
• 132697-84-8 (2R,3S)-1,3-O-benzylidene-4-octadecene-1,2,3-triol 
• 132697-85-9 (2R,3S)-1,3-O-benzylidene-2-O-methanesulfonyl-4-octadecene-1,2,3-triol 
• 3006-41-5 4,6-O-benzylidene-D-glucose 
• 25791-20-2 (n-tetradecyl)triphenylphosphonium bromide 
• 112-71-0 1-Bromotetradecane 
• 138223-65-1 (2S,3S,4E)-1,3-O-benzylidene-2-azido-4-octadecene-1,3-diol 

Relevant academic research and scientific papers

Enantiospecific Synthesis of Sphingosine and Ceramide Stereoisomers with 3S Configuration from D-Glucose

Utilizing the carbon framework (C3-C6) and chirality (at C4 and C5) of D-glucose, (2S,3S,4E and 2R,3S,4E)-2-amino-4-octadecene-1,3-diol (sphingosine analogues) and four stereoisomers (2S,3S,4E-,2S,3S,4Z-,2R,3S,4E-,and 2R,3S,4Z-) of the ceramide derivatives were synthesized in a stereocontrolled way.