201135-17-3

Upstream product

• 201135-20-8 methyl 2,3,4-tri-O-benzyl-7,8-dideoxy-α-D-manno-oct-7-enopyranoside 
• 34212-64-1 methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 124-63-0 methanesulfonyl chloride 
• 122588-59-4 methyl 2,3,4,6-tetra-O-benzyl-L-glycero-α-D-manno-heptopyranoside 

Downstream Products

• 201135-18-4 {1-[(S)-2-Benzyloxy-2-((2R,3S,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-yl)-ethyl]-piperidin-2-yl}-methanol 

Relevant academic research and scientific papers

A General Strategy to Synthesize ADP-7-Azido-heptose and ADP-Azido-mannoses and Their Heptosyltransferase Binding Properties

The multistep synthesis of a novel ADP-7-azido-7-deoxy-l-glycero-β-d-manno-heptopyranoside 2a and several analogues as heptosyltransferase ligands is described. The synthesis of the key intermediate heptoside-1-β-phosphate 3a involved a β-stereoselective

Toward a transition state analog inhibitor of N-acetylglucosaminyl transferase V

The tumor related enzyme N-acetylglucosaminyltransferase V catalyzes the transfer of GlcNAc to OH-6 of branching Man to give complex oligosaccharide structures. A transition state analog inhibitor of this enzyme was designed and a model compound was synthesized to illustrate the feasibility of the synthetic strategy.