38642-50-1

Upstream product

• 56271-35-3 2,3,5-tri-O-benzoyl-α,β-D-arabinofuranosyl bromide 
• 592-04-1 mercury(II) cyanide 
• 7677-24-9 trimethylsilyl cyanide 
• 53403-35-3 1-O-Acetyl-2,3,5-tri-O-benzoyl-α-D-arabinofuranose 
• 127676-61-3 2,5-anhydro-D-mannose oxime 
• 98-88-4 benzoyl chloride 

Downstream Products

• 127676-66-8 C₂₀H₁₇NO₅ 
• 127691-81-0 C₂₀H₁₇NO₅ 
• 127676-64-6 (2R,4S,5R)-4-Benzoyloxy-5-benzoyloxymethyl-tetrahydro-furan-2-carboxylic acid methyl ester 
• 82462-49-5 2,5-anhydro-4,6-di-O-benzoyl-3-deoxy-D-ribo-hexonic acid 
• 127676-65-7 C₂₀H₁₅NO₅ 

Relevant academic research and scientific papers

Preparation of Modified Nucleosides from Glucosamine: Rapid and Efficient Formal Total Synthesis of Several 2'-Deoxy C-Nucleosides

Formal total syntheses of several 2'-deoxy C-nucleosides have been accomplished in a short and efficient process using D-glucosamine as the starting material.

SYNTHESIS OF 2,3,5-TRI-O-BENZOYL-D-PENTOFURANOSYL CYANIDES AND THEIR CD SPECTRA

The title compounds I-IV with the respective ribo-, arabino-, xylo- and lyxo-configuration were prepared by reaction of 1-O-acetyl-2,3,5-tri-O-benzoyl-D-pentofuranoses with trimethylsilyl cyanide in 1,2-dichloroethane, catalyzed with tin tetrachloride.The