153596-70-4

Upstream product

• 18546-25-3 6-O-p-tolylsulfonyl-3,4-di-O-acetyl-D-glucal 
• 13322-79-7 (2R,3S,4R,6S)-6-Methoxy-2-methyl-tetrahydro-pyran-3,4-diol 
• 363134-99-0 diacetyl-d-glucal-6-bromohydrin 
• 90762-83-7 Methyl 3-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 100-39-0 benzyl bromide 
• 153596-68-0 Benzoic acid (2R,3R,4S,5R,6S)-4-benzyloxy-6-((2R,3R,4R,6S)-4-benzyloxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yloxy)-2-methyl-5-phenoxythiocarbonyloxy-tetrahydro-pyran-3-yl ester 
• 153596-65-7 methyl 4-O-(4-O-benzoyl-3-O-benzyl-6-deoxy-β-D-glucopyranosyl)-3-O-benzyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 2873-29-2 D-glucal triacetate 
• 76739-66-7 3,4-di-O-acetyl-D-rhamnal 
• 86651-49-2 methyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 153596-69-1 methyl 3-O-benzyl-6-(3-O-benzyl-4-O-benzoyl-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-α-D-arabino-hexopyranoside 

Downstream Products

• 153596-71-5 4-Benzyloxy-3,5-dichloro-2-methoxy-6-methyl-benzoic acid (2R,3R,4R,6S)-4-benzyloxy-6-((2R,3R,4R,6S)-4-benzyloxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yloxy)-2-methyl-tetrahydro-pyran-3-yl ester 
• 939051-48-6 methyl 3-O-benzyl-4-O-(3-O-benzyl-4-O-(3-O-benzyl-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 939051-51-1 methyl 3-O-benzyl-4-O-(3-O-benzyl-4-O-(3-O-benzyl-4-O-(3-O-benzyl-4-O-benzylsulfonyl-2,6-dideoxy-β-D-arabinohexopyranosyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 939051-57-7 methyl 3-O-benzyl-4-O-(3-O-benzyl-4-O-(3-O-benzyl-4-O-(3-O-benzyl-2,6-dideoxy-β-D-arabinohexopyranosyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-α-D-arabino-hexopyranoside 
• 939051-42-0 methyl 3-O-benzyl-4-O-(3-O-benzyl-4-O-(3-O-benzyl-4-O-benzylsulfonyl-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-β-D-arabino-hexopyranosyl)-2,6-dideoxy-α-D-arabino-hexopyranoside 

Relevant academic research and scientific papers

Direct and stereoselective synthesis of β-linked 2,6- deoxyoligosaccharides

(Chemical Equation Presented) Short and sweet: Glycosidation of 2-deoxyglycosyl imidates with I2 as shown in the scheme (Bn = benzyl, Bz = benzoyl, MS = molecular sieves) proceeds smoothly to provide the corresponding β-linked 2-deoxyglycosides

Synthesis of a terminal A-B-C disaccharide fragment of flambamycin, curamycin, and avilamycin

Methyl 2,6-dideoxy-4-O-α-D-arabino-hexopyranoside (25) corresponds to an A-B-C disaccharide subunit of the title antibiotics.It was synthesized from suitably pro