180182-57-4

Upstream product

• 52583-22-9 2,3,6-trideoxy-1,4-di-O-p-nitrobenzoyl-3-trifluoroacetamido-L-lyxopyranose 
• 122-04-3 4-nitro-benzoyl chloride 
• 54621-94-2 3,4-di-O-acetyl-L-fucal 
• 179992-16-6 Acetic acid (2S,3R,4S)-3-acetoxy-6-(4-methoxy-benzyloxy)-2-methyl-tetrahydro-pyran-4-yl ester 
• 179992-17-7 (2S,3S,4S)-6-(4-Methoxy-benzyloxy)-2-methyl-tetrahydro-pyran-3,4-diol 
• 105-13-5 4-Methoxybenzyl alcohol 
• 179992-19-9 4-Nitro-benzoic acid (2S,3S,4S)-2-methyl-6-phenylsulfanyl-4-(2,2,2-trifluoro-acetylamino)-tetrahydro-pyran-3-yl ester 
• 179992-18-8 p-Methoxybenzyl 3-O-p-nitrobenzoyl-2-deoxyfucoside 

Downstream Products

• 180182-62-1 C₄₉H₄₄F₃N₃O₂₀ 
• 169317-73-1 C₄₈H₄₂F₃N₃O₁₉ 
• 180182-58-5 p-Nitrobenzoyl 3-O-p-nitrobenzoyl-4-O-(3-N-trifluoroacetyl-4-O-p-nitrobenzoyl-α-L-daunosaminyl)-2-deoxy-L-fucoside 

Relevant academic research and scientific papers

New anthracycline disaccharides. Synthesis of L-daunosaminyl-α(1→4)-2-deoxy-L-rhamnosyl and of L-daunosaminyl-α(1→4)-2-deoxy-L-fucosyl daunorubicin analogues

The synthesis of the new disaccharide anthracyclines 20, 21, 24 and 25, where the daunosamine moiety is separated from the aglycone by either a rhamnose or a fucose residue, performed following a convergent procedure, gives insight into the configurationa