112612-41-6

Upstream product

• 67-56-1 methanol 
• 106062-15-1 lyxo-4-O-Benzylhept-1-ene-4,5,6-triol 
• 19131-10-3 methyl-2,6-didesoxy-α-L-arabino-hexopyranoside 
• 100-39-0 benzyl bromide 
• 106062-14-0 (4S,5R)-4-((R)-1-Benzyloxy-but-3-enyl)-2,2,5-trimethyl-[1,3]dioxolane 
• 106062-13-9 (2R,3S,4R)-2,3-O-isopropylidene-6-hepten-2,3,4-triol 

Downstream Products

• 151960-56-4 Toluene-4-sulfonic acid (2S,3S,4S,6R)-4-benzyloxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yl ester 
• 151960-57-5 (2S,3R,4S,6R)-3-Azido-4-benzyloxy-6-methoxy-2-methyl-tetrahydro-pyran 
• 151960-58-6 ((2S,3R,4S,6R)-4-Benzyloxy-6-methoxy-2-methyl-tetrahydro-pyran-3-yl)-dimethyl-amine 
• 67758-44-5 Methyl 2,6-dideoxy-α-L-arabino-hexopyranoside 4-p-toluenesulfonate 
• 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 

Relevant academic research and scientific papers

Definitive Synthesis of Methyl α-kedarosaminide, a Sugar Component of the Antitumor Antibiotic Kedarcidin

The first definitive synthesis and physical data of the α-methyl glycoside (methyl α-kedarosaminide (2) of kedarosamine (1), the aminodeoxy sugar component of the antibiotic kedarcidin is presented.

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