132891-83-9

Upstream product

• 34361-60-9 1,2:4,5-dicyclohexylidene-myo-inositol 
• 121702-69-0 (((2R,3S,4R)-2-(((tert-butyldimethylsilyl)oxy)methyl)-3,4-dihydro-2H-pyran-3,4-diyl)bis(oxy))bis(tert-butyldimethylsilane) 
• 13265-84-4 D-glucal 
• 111901-83-8 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-benzyl-D-myo-inositol 
• 132891-78-2 1,2;4,5-Di-O-cyclohexylidene-3-O-dibenzylphosphoryl-D-myo-inositol 
• 132915-16-3 4-O-Acetyl-2-azido-2-deoxy-3,6-di-O-tert-butyldimethylsilyl-α-D-glucopyranosyl nitrate 
• 132891-77-1 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-D-myo-inositol 
• 129094-41-3 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-dibenzylphosphoryl-D-myo-inositol 
• 132915-17-4 4-O-Acetyl-2-azido-2-deoxy-3,6-di-O-tert-butyldimethylsilyl-α-D-glucopyranosyl chloride 
• 21193-75-9 D-galactal 
• 132891-78-2 1,2;4,5-Di-O-cyclohexylidene-3-O-dibenzylphosphoryl-D-chiro-inositol 
• 132891-77-1 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-D-chiro-inositol 
• 129094-41-3 C₄₂H₅₃O₁₂P 
• 129115-29-3 6-O-Camphanoyl-1,2;4,5-di-O-cyclohexylidene-3-O-trifluoromethanesulfonyl-D-myo-inositol 

Relevant academic research and scientific papers

Synthesis and investigation of the possible insulin-like activity of 1D-4-O- and 1D-6-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-myo inositol 1-phosphate and 1D-6-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol 1,2-(cyclic phosphate)

The synthesis of the glycosyl-myo-inositol 1-phosphates 1 and 2 and of the glycosyl-myo-inositol 1,2-(cyclic phosphate) 3, starting from previously synthesized intermediates, is reported.Compound 3 was found to display proliferative effects on the early d

GLYCOSYL-INOSITOL DERIVATIVES III. SYNTHESIS OF HEXOSAMINE-INOSITOL-PHOSPHATES RELATED TO PUTATIVE INSULIN MEDIATORS

The disaccharides related to glycosyl phosphatidyl inositol anchors of membrane proteins, 4-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-D-myo-inositol-1-phosphate and 4-O-(2-amino-2-deoxy-α-D-galactopyranosyl)-D-chiro-inositol-1-phosphate, have been prepared from optically resolved myo-inositol derivatives.The chiro-inositol moiety was obtained by epimerization of a selectively blocked myo-inositol-triflate ester.The resolved inositols were subsequently phosphorylated to yield the disaccharide aglycones.The amino-sugar components were prepared by azidonitration of suitably protected glucal and galactal derivatives.The derived pyranosyl chlorides were then condensed with the inositol phosphates using silver triflate as the promoter.