191276-09-2

Upstream product

• 627466-84-6 2,3,4,6-tetra-O-benzoyl-D-galactose 
• 545-06-2 trichloroacetonitrile 
• 188435-38-3 bromide 2,3,4,6-tetra-O-Bz-α-D-galactopyranosyl bromide 
• 98-88-4 benzoyl chloride 
• 7296-64-2 β-D-galactopyranoside 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-β-D-galactopyranose 
• 2592-58-7 1,2,3,4,6-Penta-O-benzoyl-α-D-galactopyranose 

Downstream Products

• 152088-86-3 benzyl 2,4,6-tri-O-benzoyl-3-O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-β-D-galactopyranoside 
• 191276-11-6 C₃₈H₃₄O₁₁ 
• 353233-17-7 C₃₉H₃₄O₁₂ 
• 143520-25-6 cholesteryl 2,3,4,6-tetra-O-benzoyl-D-β-galactopyranoside 
• 791834-89-4 C₅₈H₇₃NO₁₆Si 
• 1137149-74-6 C₉₀H₉₄O₁₉ 
• 1303970-43-5 7-O-(2',3',4',6'-tetra-O-benzoyl-β-D-galactopyranosyl)-4-deoxy-ε-rhodomycinone 
• 125367-09-1 pent-4-enyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranoside 
• 1228755-39-2 allyl 2,3,4,6-tetra-O-benzoyl-β-D-galactopyranoside 
• 1574563-68-0 C₃₅H₃₀O₉Se 
• 483362-46-5 benzyl 2-(2,3,4,6-O-tetra-benzoyl-β-D-galactopyranosyloxy)ethylcarbamate 
• 1381857-89-1 methyl (2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Sugar/Steroid/Sugar Conjugates: Sensitivity of Lipid Binding to Sugar Structure

(Equation presented) Three steroids, each bearing a sugar on rings A and D, have been synthesized. Their effect on the "melting" behavior of a lipid bilayer depends on whether the sugar is glucose, galactose, or mannose. Packing constraints dictate how th

ENDOSOMAL CLEAVABLE LINKERS

The present disclosure relates generally to cleavable linkers and uses thereof.

Cross metathesis assisted solid-phase synthesis of glycopeptoids

A solid-phase synthesis of glycopeptoids was explored through olefin cross metathesis (CM). Peptoids and sugar derivatives with appropriate olefin moieties were coupled in the presence of an olefin metathesis catalyst to afford glycopeptoids in good yield