163379-41-7

Upstream product

• 98-88-4 benzoyl chloride 
• 153915-02-7 C₂₄H₂₃F₃O₁₀S 
• 153914-98-8 3-Azido-5-O-benzoyl-4-C-benzoyloxymethyl-3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 
• 153914-97-7 5-O-benzoyl-4-benzoyloxymethyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 55797-64-3 1,2-O-isopropylidene-4-C-(hydroxymethyl)-β-L-threo-pento-1,4-furanose 
• 108-24-7 acetic anhydride 

Downstream Products

• 163215-15-4 1-(2-O-acetyl-3-azido-5-O-benzoyl-4-benzoyloxymethyl-3-deoxy-β-D-ribofuranosyl)-N⁴-acetylcytosine 
• 163215-14-3 9-(2-O-acetyl-3-azido-5-O-benzoyl-4-benzoyloxymethyl-3-deoxy-β-D-ribofuranosyl)-N⁶-benzoyladenine 
• 153915-01-6 9-(2-O-acetyl-3-azido-5-O-benzoyl-4-benzoyloxymethyl-3-deoxy-β-D-ribofuranosyl)uracil 
• 153915-01-6 1-(2-O-acetyl-3-azido-5-O-benzoyl-4-benzoyloxymethyl-3-deoxy-β-D-ribofuranosyl)uracil 

Relevant academic research and scientific papers

Novel 4'-branched nucleosides

Total chemical synthesis of 4'-hydroxymethylnucleosides with an additional modification in a sugar residue was developed. The synthesis was made by condensation of corresponding protected sugars and nucleic bases with subsequent deprotection. In such a wa

4'-BRANCHED NUCLEOSIDES. I. SYNTHESIS OF 3'-AMINO-4'-HYDROXYMETHYL-3'-DEOXYNUCLEOSIDES

The glycosylation of trimethylsilyl derivatives of N6-benzoyladenine, N4-acetylcytosine, and uracil with 1,2-di-O-acetyl-3-azido-5-O-benzoyl-4-benzoyloxymethyl-3-deoxy-β-D-ribofuranose in the presence of SnCl4 and subsequent deacylat