170900-79-5

Upstream product

• 23393-20-6 D-1-O-benzyl-2,3:5,6-di-O-cyclohexylidene-myo-inositol 
• 154459-84-4 1L-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzoyl)-myo-inositol 
• 164904-89-6 6-O-allyl-3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-L-myo-inositol 
• 154459-83-3 1L-6-O-allyl-3-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 131233-71-1 1D-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 
• 100-39-0 benzyl bromide 
• 579494-16-9 3,4,5,6-tetra-O-benzyl-1-O-(4-methoxybenzyl)-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->2)-L-myo-inositol 
• 169106-94-9 2-O-acetyl-3,4,6-tri-O-benzyl-α/β-D-mannopyranosyl fluoride 

Relevant academic research and scientific papers

Synthesis of phosphatidylinositol mannosides (PIMs)

Two strategies towards the synthesis of phosphatidylinositol mannosides (PIMs) were elaborated which permit selective access to the O-1-, O-2-, and the O-6 position of the myo-inositol residue. Starting materials are 1,2:5,6- and 1,2:4,5-di-O-cyclohexylid

The synthesis of 1-O-(2-N-stearoyl-D-erythro-sphinganine-1-phosphoryl)-2-O-(α-D-mannopyranosyl-D-myo-inositol: a fragment of the naturally occurring inositol-containing glycophosphosphingolipids

Chiral mannosylinositol containing sphingophospholipid was synthesized from D-erythro ceramide and optically active mannosyl-myo-inositol with the use of phosphite triester coupling procedure.The optical resolution of racemic 3,4,5,6-tetra-O-benzyl-myo-in