3868-01-7

Upstream product

• 107908-97-4 methyl 2,6-dideoxy-3-O-benzyl-α-D-lyxo-hexopyranoside 
• 74-88-4 methyl iodide 
• 4833-12-9 methyl 4-O-acetyl-3-O-benzyl-2,6-dideoxy-α-D-lyxo-hexopyranoside 
• 1128-40-1 methyl 6-deoxy-α-D-talopyranoside 
• 106062-13-9 (2R,3S,4R)-2,3-O-isopropylidene-6-hepten-2,3,4-triol 
• 106062-15-1 lyxo-4-O-Benzylhept-1-ene-4,5,6-triol 
• 63592-82-5 (2R,3S,4R)-4-Benzyloxy-6-methoxy-2-methyl-tetrahydro-pyran-3-ol 
• 100-39-0 benzyl bromide 
• 106062-14-0 (4S,5R)-4-((R)-1-Benzyloxy-but-3-enyl)-2,2,5-trimethyl-[1,3]dioxolane 
• 151834-84-3 methyl 6-deoxy-3,4-O-isopropylidene-2-O-<(methylthio)thiocarbonyl>-α-D-talopyranoside 
• 151908-76-8 methyl 6-deoxy-3,4-O-isopropylidene-α-D-talopyranoside 
• 75810-11-6 Methyl-2,6-didesoxy-3,4-O-isopropyliden-α-D-lyxo-hexopyranosid 
• 104846-19-7 methyl 6-deoxy-2,3-O-isopropylidene-α-D-talopyranoside 
• 13322-79-7 methyl 2,6-dideoxy-α-D-lyxo-hexopyranoside 

Downstream Products

• 106023-22-7 (2R,3S,4R)-4-Benzyloxy-3-methoxy-2-methyl-6-phenylsulfanyl-tetrahydro-pyran 
• 131013-41-7 tert-Butyldimethylsilyl 4-O-Acetyl-3-(3-O-benzyl-2,6-dideoxy-4-O-methyl-β-D-lyxo-pyranosyl)-2,6-dideoxy-β-D-lyxo-pyranoside 
• 131013-40-6 tert-Butyldimethylsilyl 4-O-Acetyl-3-(3-O-benzyl-2,6-dideoxy-4-O-methyl-α-D-lyxo-pyranosyl)-2,6-dideoxy-β-D-lyxo-pyranoside 
• 131013-38-2 tert-Butyldimethylsilyl 4-O-Acetyl-3-(3-O-benzyl-2,6-dideoxy-4-O-methyl-α-D-lyxo-pyranosyl)-2,6-dideoxy-α-D-lyxo-pyranoside 
• 106023-24-9 Acetic acid (2R,3S,4R,6S)-4-((2R,4R,5S,6R)-4-benzyloxy-5-methoxy-6-methyl-tetrahydro-pyran-2-yloxy)-6-methoxy-2-methyl-tetrahydro-pyran-3-yl ester 
• 69282-20-8 α-D-rubranitrose 
• 69282-20-8 β-D-rubranitrose 

Relevant academic research and scientific papers

Investigation of Different Synthetic Approaches towards Methyl 2,6-Dideoxy-α-D-arabino- and -α-D-lyxo-hexopyranosides

New synthetic routes for making available different methyl 2,6-dideoxyhexopyranosides are reported.Starting with methyl 6-deoxy-2,3-O-isopropylidene-α-D-manno- and -α-D-talo-pyranoside the respective methyl 2,6-dideoxy-α-D-arabino- and α-D-lyxo-hexopyrano

A Highly Stereoselective Synthesis of the AB Disaccharide Unit of Olivomycin A

A highly stereoselective synthesis of the AB disaccharide (4c) of olivomycin A is described.The synthesis features the double asymmetric allylboration of α,β-dialkoxy aldehyde 8 using tartrate allylboronate (S,S)-9, which provides triol derivative 10 with