1573119-89-7

Upstream product

• 545-06-2 trichloroacetonitrile 

Downstream Products

• 1573119-87-5 allyl 2-O-acetyl-4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-β-D-glucopyranosyl-(1→2)-6-O-tert-butyldimethylsilyl-3,4-O-isopropylidene-α-D-galactopyranoside 
• 1573119-90-0 allyl 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-β-D-glucopyranosyl-(1→2)-6-O-tert-butyldimethylsilyl-3,4-O-isopropylidene-α-D-galactopyranoside 
• 1573119-91-1 allyl 4,6-O-benzylidene-2-O-tert-butyldimethylsilyl-β-D-glucopyranosyl-(1→2)-6-O-tert-butyldimethylsilyl-3,4-O-isopropylidene-α-D-galactopyranoside 
• 1573119-92-2 allyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl (1→2)-4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-β-D-glucopyranosyl-(1→2)-6-O-tert-butyldimethylsilyl-3,4-O-isopropylidene-α-D-galactopyranoside 
• 1573120-03-2 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl (1→2)-4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-β-D-glucopyranosyl(1→2)-6-O-tert-butyldimethylsilyl-3,4-O-isopropylidene-α-D-galactopyranose 

Relevant academic research and scientific papers

Synthesis of the trisaccharide moiety and a cholesteryl analog of phyteumosides

A first synthesis of the trisaccharide moiety of the phyteumosides and its cholesteryl analog is described using easily accessible and regioselectively protected d-glucose, l-rhamnose and d-galactose building blocks via a linear glycosylation approach. Th