101072-27-9

Upstream product

• 108-24-7 acetic anhydride 
• 74766-86-2 DL-3,4-di-O-Acetyl-1,2-anhydro-(1,2,3/4)-5-benzoyloxymethyl-5-cyclohexene-1,2,3,4-tetrol 
• 96291-88-2 (1R)-3,4-di-O-acetyl-1,2-anhydro-(1,2,3/4)-5-<(benzoyloxy)methyl>-5-cyclohexene-1,2,3,4-tetrol 
• 20881-87-2 Methyl 4-amino-4,6-dideoxy-α-D-mannopyranoside 
• 141232-01-1 Methyl 4-azido-4-deoxy-2,3-O-isopropylidene-6-O-p-toluenesulfonyl-α-D-mannopyranoside 
• 15856-44-7 Methyl 4-acetamido-4,6-dideoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 92735-13-2 methyl 4-azido-4-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 20197-44-8 Methyl 4-acetamido-2,3-di-O-acetyl-4,6-dideoxy-α-D-mannopyranoside 
• 13042-64-3 Methyl 4-amino-4,6-dideoxy-α-D-glucopyranoside 

Downstream Products

• 141316-50-9 Methyl 4,6-dideoxy-4-<(1S)-(1,4/5,6)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-ylamino>-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis and enzyme-inhibitory activity of methyl acarviosin analogues having the α-manno configuration

Two methyl acarviosin analogues 3a and 4a, having the α-manno configuration, and their dihydro derivatives 6a and 7a were synthesized by coupling the protected pseudo-sugar epoxides with methyl 4-amino-4-deoxy- and -4,6-dideoxy-α-D-mannopyranoside.Similar