143446-81-5

Upstream product

• 143446-80-4 D-2,4,5,6-Tetra-O-benzyl-3-deoxy-3-fluoro-myo-inositol 1- 
• 143446-79-1 D-2,4,5,6-Tetra-O-benzyl-3-deoxy-3-fluoro-myo-inositol 1-(O-benzyl-N,N-diisopropylphosphoramidite) 
• 143446-78-0 D-2,4,5,6-Tetra-O-benzyl-3-deoxy-3-fluoro-1-O-(methoxymethyl)-myo-inositol 
• 142544-21-6 D-2,4,5,6-Tetra-O-benzyl-3-deoxy-3-fluoro-myo-inositol 
• 151071-93-1 D-4,5,6-Tri-O-benzyl-3-deoxy-3-fluoro-1-O-(methoxymethyl)-myo-inositol 
• 151071-90-8 D-4,5,6-Tri-O-benzyl-3-deoxy-3-fluoro-1,2-O-isopropylidene-myo-inositol 
• 143446-77-9 D-4,5,6-Tri-O-benzyl-3-deoxy-3-fluoro-myo-inositol 
• 143446-76-8 D-3-Deoxy-3-fluoro-1,2-O-isopropylidene-myo-inositol 
• 642-38-6 quebrachitol 
• 125290-99-5 (1S,2S,3R,4S,5S,6S)-1-fluoro-2-O-(methyl)cyclohexane-2,3,4,5,6-pentol 
• 120444-24-8 D-3-deoxy-3-fluoro-myo-inositol 
• 30334-71-5 1,2-dipalmitoyl-sn-glycerol 

Relevant academic research and scientific papers

Synthesis and biological activity of the D-3-deoxy-3-fluoro and D-3-chloro-3-deoxy analogues of phosphatidylinositol

The naturally occurring inositol derivative, L-quebrachitol (1), serves as starting material for the synthesis of D-3-deoxy-3-fluoro- and D-3-chloro-3-deoxy-myo-inositol (4, 28). Their transformation into the title compounds 22 and 40 (abbreviated as FPI