141232-10-2

Upstream product

• 141232-04-4 2,3-Di-O-acetyl-1,6-anhydro-4-O-p-toluenesulfonyl-β-D-mannopyranose 
• 141232-05-5 2,3-Di-O-acetyl-1,6-anhydro-4-azido-4-deoxy-β-D-mannopyranose 
• 5349-02-0 1,6-Anhydro-2,3-O-isopropylidene-4-O-p-toluenesulfonyl-β-D-mannopyranose 
• 14440-51-8 1,6-anhydro-2,3-O-isopropylidene-β-D-mannopyranose 
• 68354-63-2 4-Acetamido-2,3-di-O-acetyl-1,6-anhydro-4-deoxy-β-D-mannopyranoside 
• 68354-61-0 4-Amino-1,6-anhydro-4-deoxy-β-D-mannopyranose 
• 108-24-7 acetic anhydride 
• 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 

Downstream Products

• 141316-52-1 1,6-Anhydro-4-deoxy-4-<(1S)-(1,4/5,6)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-ylamino>-β-D-mannopyranose 

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