145149-83-3

Upstream product

• 138665-01-7 Methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-ribo-hexopyranoside 
• 145149-84-4 Methyl 6-O-acetyl-2,4-di-O-benzyl-3-deoxy-α-D-ribo-hexopyranoside 
• 50272-14-5 methyl 2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-ribo-hexopyranoside 
• 100-44-7 benzyl chloride 
• 65530-28-1 methyl 4,6-O-benzylidene-3-deoxy-α-D-glucopyranoside 
• 3150-16-1 methyl 4,6-O-benzylidene-2,3-anhydro-α-D-mannopyranoside 
• 34266-73-4 methyl 4,6-O-benzylidene-3-deoxy-α-D-arabino-hexopyranoside 
• 40773-64-6 methyl 4,6-O-benzylidene-3-deoxy-ribo-hexopyranoside 
• 76375-66-1 methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside 
• 145149-81-1 methyl 2-O-benzyl-4,6-O-benzylidene-3-O-(phenylthionocarbonate)-α-D-glucopyranoside 

Downstream Products

• 152838-18-1 dimethyl <(3R,5R)-dibenzyloxy-7-tert-butyldiphenylsilyloxy-heptan-2-on-1-yl> phosphonate 
• 152838-17-0 methyl (2R,4R)-dibenzyloxy-6-tert-butyldiphenylsilyloxy-hexanoate 
• 152838-15-8 (2R,4R)-dibenzyloxy-6-tert-butyldiphenylsilyloxy-1,1-dimethoxy-hexane 
• 152838-16-9 (2R,4R)-dibenzyloxy-6-tert-butyldiphenylsilyloxy-hexanal 
• 152838-13-6 (2R,4S)-dibenzyloxyhex-5-enal 
• 152838-14-7 (2R,4S)-dibenzyloxy-1,1-dimethoxy-hex-5-ene 
• 152838-12-5 methyl 2,4-di-O-benzyl-3,6-dideoxy-6-iodo-α-D-ribo-hexopyranoside 
• 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 

Relevant academic research and scientific papers

A Carbohydrate Approach to Polyol Fragments of Amphotericin and the Trienomycin- and Mycotrienin Antibiotics

Hydrolytically labile ω-chloro-ω-phenylthioglycosides, obtained from the corresponding ω-phenylthioglycosides on treatment with NCS in CCl4, are readily dealkoxyhalogenated with Zn/Ag-graphite in anhydrous solvents affording enantiomerically pure synthons

Regioselectivity of Reductive Cleavage of Methyl 4,6-O-Benzylidene-3-deoxyhexopyranosides Containing Fluorine at the 2- or 3-Position with LiAlH4-AlCl3

Reductive ring-opening reactions of the 4,6-O-benzylidene derivatives of methyl 3-deoxy-β-D-arabino-, 3-deoxy-α-D-ribo-, and 2-O-benzyl-3-deoxy-α-D-ribo-hexopyranosides with LiAlH4 and AlCl3 in the molar ratio of 4:4 gave the 4- and 6-O-benzyl derivatives

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