85230-78-0

Upstream product

• 62346-15-0 methyl 2,6-dideoxy-β-L-lyxo-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 
• 67-56-1 methanol 
• 106062-15-1 lyxo-4-O-Benzylhept-1-ene-4,5,6-triol 

Downstream Products

• 4833-12-9 methyl 4-O-acetyl-3-O-benzyl-2,6-dideoxy-α-D-lyxo-hexopyranoside 
• 3868-01-7 methyl 2,6-dideoxy-3-O-benzyl-4-O-methyl-α-D-lyxo-hexopyranoside 
• 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 
• 106023-22-7 (2R,3S,4R)-4-Benzyloxy-3-methoxy-2-methyl-6-phenylsulfanyl-tetrahydro-pyran 
• 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 
• 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 
• 131013-41-7 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 
• 85230-80-4 methyl-4-O-(4-O-acetyl-2,3,6-tridesoxy-2-iodo-α-L-arabino-hexopyranosyl)-3-O-benzyl-2,6-didesoxy-β-L-lyxo-hexopyranoside 
• 85230-80-4 methyl-4-O-(4-O-acetyl-2,3,6-tridesoxy-2-iodo-β-L-ribo-hexopyranosyl)-3-O-benzyl-2,6-didesoxy-β-L-lyxo-hexopyranoside 
• 86964-38-7 methyl 3-O-benzyl-4-O-acetyl-2-deoxy-β-L-fucoside 
• 114517-86-1 methyl-3-O-benzyl-2,6-didesoxy-4-O-p-toluenesulfonyl-β-L-lyxo-hexopyranoside 
• 86964-41-2 benzyl 4-O-(3-O-benzyl-2,6-dideoxy-α-L-lyxo-hexopyranosyl)-2,3,6-trideoxy-3-trifluoroacetamido-α-L-lyxo-hexopyranoside 

Relevant academic research and scientific papers

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

SYNTHESE DES METHYL-2,4,6-TRIDESOXY-4-TRIFLUOROACETAMIDO-L-HEXOPYRANOSIDES. ACCES A DE NOUVELLES ANTHRACYCLINES

The four diastereoisomeric methyl 2,4,6-trideoxy-4-trifluoroacetamido-L-hexopyranosides have been synthesized.Coupling of the corresponding 1-O-acetyl-3-O-benzoyl-L-lyxo and 1-O-acetyl-3-O-p-nitrobenzoyl-L-arabino derivatives with daunomycinone in the pre

SYNTHESE DE DISACCHARIDES NATURELS, FRAGMENTS D'ANTHRACYCLINES OLIGOSACCHARIDIQUES

Methyl 2,6-dideoxy-4-O-(2,3,6-trideoxy-α-L-glycero-hexopyranosyl-4-ulose-β-L-lyxo-hexopyranoside and methyl 2,6-dideoxy-4-O-(2,3,6-trideoxy-α-L-erythro-hexopyranosyl)-β-L-lyxo-hexopyranoside, fragments of C->B type of trisaccharides naturally occurring in