145149-81-1

Upstream product

• 76375-66-1 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 1005-56-7 phenylcarbonochloridothioate 

Downstream Products

• 365418-34-4 methyl 2-O-benzyl-4,6-di-O-benzylidene-3-allyl-3-deoxy-α-D-glucopyranoside 
• 145149-89-9 Methyl O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1->6)-O-(2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1->6)-2,4-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside 
• 145149-84-4 Methyl 6-O-acetyl-2,4-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside 
• 145149-83-3 Methyl 2,4-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside 
• 138665-01-7 Methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-ribo-hexopyranoside 

Relevant academic research and scientific papers

Designing an effective approach for obtaining methylenecarboxylate analogues of adenophostin A. Preliminary results

Preliminary results for the synthesis of two new adenophostin analogues incorporating 3″- and 4″-methylenecarboxylate surrogate groups are presented. The synthesis involves the preparation of 3″- and 4″-methylenecarboxylate glucose derivatives by a radica

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