63592-82-5

Upstream product

• 100-39-0 benzyl bromide 
• 106062-13-9 (2R,3S,4R)-2,3-O-isopropylidene-6-hepten-2,3,4-triol 
• 106062-14-0 (4S,5R)-4-((R)-1-Benzyloxy-but-3-enyl)-2,2,5-trimethyl-[1,3]dioxolane 
• 67-56-1 methanol 
• 106062-15-1 lyxo-4-O-Benzylhept-1-ene-4,5,6-triol 
• 64951-98-0 methyl 3-O-benzyl-2-deoxy-α-D-ribo-hexopyranoside 
• 90761-25-4 methyl 3-O-benzyl-4,6-O-benzylideno-2-deoxy-α-D-ribo-hexoside 
• 6752-48-3 methyl 2-deoxy-4,6-O-benzylidene-α-D-ribo-hexopyranoside 
• 4092-45-9 methyl 2,6-dideoxy-α-D-ribo-hexopyranoside 

Downstream Products

• 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 
• 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 
• 131013-41-7 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 
• 131041-37-7 4-O-Acetyl-3-(3-O-benzyl-2,6-dideoxy-4-O-methyl-α-D-lyxo-pyranosyl)-2,6-dideoxy-α-D-lyxo-pyranose 
• 131013-42-8 4-O-Acetyl-3-(3-O-benzyl-2,6-dideoxy-4-O-methyl-α-D-lyxo-pyranosyl)-2,6-dideoxy-β-D-lyxo-pyranose 
• 106023-22-7 (2R,3S,4R)-4-Benzyloxy-3-methoxy-2-methyl-6-phenylsulfanyl-tetrahydro-pyran 
• 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 
• 3868-01-7 methyl 2,6-dideoxy-3-O-benzyl-4-O-methyl-α-D-lyxo-hexopyranoside 
• 4833-12-9 methyl 4-O-acetyl-3-O-benzyl-2,6-dideoxy-α-D-lyxo-hexopyranoside 
• 148944-25-6 Methyl 4-azido-3-O-benzyl-2,4,6-trideoxy-α-D-xylo-hexopyranoside 
• 63592-81-4 Methyl 3-O-benzyl-2,6-dideoxy-4-O-tosyl-α-D-ribo-hexopyranoside 

Relevant academic research and scientific papers

Deleterious effect of 7-methyl group on glycosylation of 2-naphthols

C-Glycosylations of several 2-naphthols with different glycosyl donors have been investigated in the pursuit of the total synthesis of mayamycin (1). While glycosylations of the parent 2-naphthol are readily achievable, those of 5-methoxy-7-methyl-2-napht

Synthesis of cyclophosphamide analogs from aminotrideoxy sugars

Cyclophosphamide 1a is a highly effective and extensively used agent for the treatment of human cancers. The metabolism, pharmacokinetics, and mechanism of action of 1a are frequently reviewed. By analogy with well known strategy in the design of potentia

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