1447464-00-7

Upstream product

• 1447463-96-8 bis((R)-2-cyano-1-phenylethyl) diisopropylphosphoramidite 
• 1447463-99-1 (1R,2r,3S,4R,5r,6S)-2,4,5,6-tetrakis((4-methoxybenzyl)oxy)cyclohexane-1,3-diol 
• 824-94-2 p-methoxybenzyl chloride 
• 73627-97-1 (R)-3-phenyl-3-hydroxypropanenitrile 

Downstream Products

• 1447464-03-0 bis((R)-2-cyano-1-phenylethyl) ((1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl)phosphate 
• 106032-59-1 D-myo-inositol 1-phosphate biscyclohexylammonium salt 

Relevant academic research and scientific papers

Desymmetrization of myo-inositol derivatives by lanthanide catalyzed phosphitylation with C2-symmetric phosphites

Desymmetrization by phosphorylation represents a promising method with potential impact in many different areas of research. C2-Symmetric phosphoramidites have been used to desymmetrize myo-inositol derivatives by functionalization at different

Synthesis of unsymmetric diphospho-inositol polyphosphates

One to rule them all: A novel C2-symmetric phosphoramidite was developed that can be used to prepare all four unsymmetric diphospho inositol pentaphosphates (PP-InsP5). The target structures were synthesized in few steps and high enantiomeric ratios. With the obtained compounds, specificity of Ddp1 from yeast (a PP-InsP5 phosphatase) was studied. Copyright