215869-70-8

Upstream product

• 100-39-0 benzyl bromide 
• 824-94-2 p-methoxybenzyl chloride 
• 215869-20-8 (1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol 
• 202798-29-6 3,4,5,6-tetra-O-benzyl-D-chiro-inositol 

Downstream Products

• 79391-04-1 O-α-D-galactopyranosyl-(1->2)-D-chiroinositol 
• 215869-71-9 (2R,3S,4S,5R,6R)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-6-((2S,3R,5R,6S)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyloxy)-tetrahydro-pyran 

Relevant academic research and scientific papers

Stereoselective α-glycosylation of C(6)-hydroxyl myo-inositols via nickel catalysis - Application to the synthesis of GPI anchor pseudo-oligosaccharides

Glycosylphosphatidyl inositol (GPI) anchors play a key role in many eukaryotic biological pathways. Stereoselective synthesis of GPI anchor analogues have proven to be critical for probing the biosynthesis, structure, and biological properties of these co

Synthesis of a jojoba bean disaccharide

A synthesis of the disaccharide recently isolated from jojoba beans, 2-O-α-D-galactopyranosyl-D-chiro-inositol, has been achieved. The suitably protected chiro-inositol unit was prepared by an enantiospecific synthesis from L-xylose utilizing SmI2-mediated pinacol coupling as a key step. Copyright (C) 1998 Elsevier Science Ltd.