154459-83-3

Upstream product

• 23393-20-6 D-1-O-benzyl-2,3:5,6-di-O-cyclohexylidene-myo-inositol 
• 154459-93-5 1L-6-O-allyl-3-O-benzyl-1,2:4,5-di-O-cyclohexylidene-myo-inositol 

Downstream Products

• 164904-89-6 6-O-allyl-3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-L-myo-inositol 
• 131233-71-1 1D-4-O-allyl-1,5,6-tri-O-benzyl-myo-inositol 
• 154459-84-4 1L-6-O-allyl-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzoyl)-myo-inositol 
• 170900-79-5 3,4,5,6-tetra-O-benzyl-2-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->2)-L-myo-inositol 
• 154459-85-5 1L-2,3,4,5-tetra-O-benzyl-1-O-(4-methoxybenzoyl)-myo-inositol 

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

Parasite Glucoconjugates. Part 1. The Synthesis of Some Early and Related Intermediates in the Biosynthetic Pathway of Glycosyl-phosphatidylinositol Membrane Anchors

The enantio-pure 1D- and 1L-myo-inositol derivative 3D and 3L have been used to prepare sodium 1D-6-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol sn-2,3-dipalmitoyloxypropyl phosphate 21 and a related 1,6-disubstituted 1L-myo-inositol 28, respective