858127-27-2

Upstream product

• 858127-26-1 p-methoxyphenyl 3,4,6-tri-O-benzyl-2-O-methoxycarbonyl-β-D-galactopyranosyl-(1->3)-4,6-O-benzylidene-2-deoxy-2-azido-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 247027-79-8 p-methoxyphenyl 2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 858127-24-9 p-methoxyphenyl 3,4,6-tri-O-acetyl-2-deoxy-2-azido-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-β-D-galactopyranoside 
• 858127-25-0 (2S,4aR,6S,7R,8R,8aR)-7-Azido-6-[(2R,3S,4S,5R,6S)-3,5-bis-benzyloxy-2-benzyloxymethyl-6-(4-methoxy-phenoxy)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-ol 
• 858127-20-5 2,2,2-Trifluoro-N-phenyl-acetimidic acid (2S,3R,4S,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-methoxycarbonyloxy-tetrahydro-pyran-2-yl ester 

Relevant academic research and scientific papers

Versatile use of ytterbium(III) triflate and acid washed molecular sieves in the activation of glycosyl trifluoroacetimidate donors. Assemblage of a biologically relevant tetrasaccharide sequence of Globo H

The nonreducing tetrasaccharide terminus of Globo H has been assembled in good yield and excellent stereocontrol exclusively by using mild and moisture stable agents such as Yb(OTf)3 and acid washed molecular sieves for the activation of glycos