870195-61-2

Upstream product

• 212192-84-2 ethyl 2-O-acetyl-4,6-di-O-benzyl-1-thio-α-D-mannopyranoside 
• 441017-58-9 6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl iodide 
• 100-39-0 benzyl bromide 
• 870195-60-1 ethyl 6-O-acetyl-1-thio-α-D-mannopyranoside 
• 7473-36-1 ethyl 1-thio-α-D-mannopyranoside 

Downstream Products

• 870195-62-3 ethyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl-(1->3)-2,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside 

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

Synthesis of the tetrasaccharide α-D-Glcp-(1→3)-α-D-Manp- (1→2)-α-D-Manp-(1→2)-α-D-Manp recognized by Calreticulin/Calnexin

The title compound as its methyl glycoside was efficiently synthesized using a block synthesis approach. Halide-assisted glycosidations between 6-O-acetyl-2,3,4-tri-O-benzyl-α-d-glucopyranosyl iodide and ethyl 2-O-acetyl-4,6-di-O-benzyl-1-thio-α-d-mannopy