5540-29-4

Upstream product

• 76-83-5 trityl chloride 
• 24578-12-9 Methyl 3,4-anhydro-α-D-galactopyranoside 
• 31505-47-2 methyl 2,3-di-O-acetyl-4-O-(methylsulfonyl)-6-O-triphenylmethyl-α-D-glucopyranoside 
• 67-56-1 methanol 
• 67-66-3 chloroform 
• 124-41-4 sodium methylate 
• 20231-37-2 methyl 2,3-di-O-benzoyl-4-O-(p-tolylsulfonyl)-6-O-trityl-α-D-glucopyranoside 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 67-64-1 acetone 
• 19488-44-9 methyl 2,3-di-O-benzoyl-4-O-(p-tolylsulfonyl)-α-D-glucopyranoside 
• 29868-42-6 methyl 2,3-di-O-acetyl-α-D-glucopyranoside 
• 53717-00-3 methyl 2,3-di-O-acetyl-6-O-trityl-α-D-glucopyranoside 

Downstream Products

• 123878-79-5 methyl-(O²-acetyl-O⁶-trityl-3,4-anhydro-α-D-galactopyranoside) 
• 142504-78-7 methyl 3,4-anhydro-2-O-tetrahydropyranyl-6-O-triphenylmethyl-α-D-galactopyranoside 
• 142504-76-5 methyl 3,4-anhydro-2-O-methyl-6-O-triphenylmethyl-α-D-galactopyranoside 
• 6027-89-0 L-gulose 
• 97-30-3 methyl-alpha-D-glucopyranoside 

Relevant academic research and scientific papers

Chemical modification of the sugar part of methyl acarviosin: Synthesis and inhibitory activities of nine analogues

Nine analogues of methyl acarviosin (1), the core structure of acarbose and its homologues, the 6-hydroxy-(2), 6-azido-(3), 6-amino-(4), 6-acctamido-(5), 6-methoxy-(6), 6-hydroxy-2-O-methyl-(8), and 6-hydroxy-3-O-methyl derivatives (9), including the 5-me