154618-73-2

Upstream product

• 4163-60-4 β-D-galactose peracetate 
• 3068-32-4 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside 
• 154618-72-1 phenyl 2,3,4,6-tetra-O-acetyl-1-seleno-β-D-galactopyranoside 
• 1666-13-3 diphenyl diselenide 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 4981-97-9 phenyl 1-seleno-β-D-galactopyranoside 

Downstream Products

• 161953-89-5 phenyl 2,3,4-tri-O-benzyl-6-O-tert-butyldimethylsilyl-1-seleno-β-D-galactopyranoside 
• 143995-70-4 C₆₇H₆₂O₁₃Se 
• 143995-71-5 C₆₇H₆₂O₁₃Se 
• 143995-69-1 C₃₃H₂₈O₈Se 

Relevant academic research and scientific papers

The Use Of Selenophenyl Galactopyranosides for the Synthesis of α- and β-(1->4)-C-Disaccharides

Methyl α-C-lactoside 4)-α-D-Glcp-OMe> and its α anomer were expeditiously synthesized by radical coupling of various selenophenyl galactopyranosides onto methyl 2,3-di-O-benzyl-4-deoxy-4-C-methylene-α-D-xylo-hexopyranoside, which are tempor

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