918334-61-9

Upstream product

• 53008-62-1 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl iodide 
• 799267-94-0 2,3,4,6-tetra-O-benzyl-1-deoxy-α-D-galactopyranosylethene 
• 3396-99-4 methyl α-D-galactopyranoside 
• 53008-63-2 methyl 2,3,4,6-tetra-O-benzyl-α-D-galactopyranoside 
• 918334-60-8 4-C-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-3-E-butene-1,2(S)-di-O-acetate 
• 57-10-3 1-hexadecylcarboxylic acid 

Downstream Products

• 918334-62-0 4-C-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-1-O-palmitoyl-2(S)-O-stearoyl-3-E-butene 

Relevant academic research and scientific papers

Glycosyl iodides. History and recent advances

The use of glycosyl iodides as an effective method for the preparation of glycosides has had a recent resurgence in carbohydrate chemistry, despite its early roots in which these species were believed to be of limited use. Renewed interest in these specie

Efficient synthesis of a C-analogue of the immunogenic bacterial glycolipid BbGL2

(Diagram presented) Synthesis of a C-analogue of bacterial glycolipid BbGL2 is reported using Grignard reaction of in situ generated β-galactosyl iodide and subsequent olefin cross metathesis reaction of C-vinyl galactoside as key steps.