128537-01-9

Upstream product

• 108-24-7 acetic anhydride 
• 138665-01-7 Methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-ribo-hexopyranoside 

Downstream Products

• 128537-06-4 Methyl 2,6-di-O-benzyl-3-deoxy-4-(O-methylsulfonyl)-α-D-ribo-hexopyranoside 
• 128537-08-6 Methyl 2,6-di-O-benzyl-3-deoxy-4-O-(methylsulfonyl)-α-D-xylo-hexopyranoside 
• 128537-03-1 (2R,3R,5R,6S)-5-Benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-ol 
• 128537-07-5 Methyl 4-O-benzoyl-2,6-di-O-benzyl-3-deoxy-α-D-xylo-hexopyranoside 
• 128537-09-7 Methyl 4-azido-2,6-di-O-benzyl-3,4-dideoxy-α-D-ribo-hexopyranoside 
• 128537-13-3 methyl 2,6-di-O-benzyl-4,5-didehydro-3,4-dideoxy-α-D-glucopyranoside 
• 117371-67-2 Methyl 2,6-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside 

Relevant academic research and scientific papers

Syntheses of specifically deoxygenated methyl α-isomaltotriosides

Specifically deoxygenated methyl α-isomaltotriosides were synthesized by the silver perchlorate-mediated condensation of a protected α-isomaltosyl chloride with suitably blocked derivatives of methyl α-D-glucopyranoside deoxygenated respectively at positi