131919-44-3

Upstream product

• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 40653-32-5 methyl 2,3,4-tri-O-benzyl-β-D-galactopyranoside 
• 143995-68-0 2,3,4,6-tetra-O-benzoyl-β-D-selenogalactopyranoside 
• 4163-60-4 β-D-galactose peracetate 
• 154618-72-1 phenyl 2,3,4,6-tetra-O-acetyl-1-seleno-β-D-galactopyranoside 
• 4981-97-9 phenyl 1-seleno-β-D-galactopyranoside 
• 98-88-4 benzoyl chloride 

Relevant academic research and scientific papers

Iodonium Ion-Mediated Glycosidations of Phenyl Selenoglycosides

Fully benzylated or benzoylated phenyl selenoglycosides can be activated by the promoters iodonium di-sym-collidine perchlorate (IDCP) or N-iodosuccinimide and catalytic triflic acid (NIS/TfOH cat.).The potential of the iodonium ion-mediated glycosidation

A Highly Efficient Synthesis of Tri-O-Acyl-α-D-Glucopyranose 1,2-(Orthoesters) under High Pressure

High pressure-assisted condensation reaction of acylated glucosyl bromides with complex alcohols in the presence of diisopropylethylamine and tetrabutylammonium bromide gave the corresponding 1,2-orthoesters in good to excellent yields without using heavy