145149-91-3

Upstream product

• 145149-88-8 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)-2,3-di-O-benzoyl-4-deoxy-α-D-xylo-hexopyranoside 
• 79330-96-4 phenyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-methylsulfonylethoxycarbonyl-1-thio-β-D-glucopyranoside 
• 139302-22-0 Methyl 2,3-di-O-benzoyl-4-deoxy-α-D-xylo-hexopyranoside 
• 145149-79-7 Methyl 2,3-di-O-benzoyl-6-O-benzyl-4-deoxy-α-D-xylo-hexopyranoside 
• 145149-78-6 Methyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(imidazol-1-ylthiocarbonyl)-α-D-glucopyranoside 
• 145149-80-0 Methyl 2,3-di-O-benzoyl-6-O-benzyl-4-O-(phenoxythiocarbonyl)-α-D-glucopyranoside 
• 145149-77-5 O-(6-O-Acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranosyl chloride 
• 145149-86-6 O-(6-O-Acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1->6)-1-O-acetyl-2,3,4-tri-O-benzyl-α,β-D-glucopyranose 

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