201853-73-8

Upstream product

• 67-56-1 methanol 
• 201853-71-6 methyl [2-deoxy-3-O-(p-toluoyl)-α-D-ribofuranosiduronic acid] 
• 452-51-7 D-2-deoxyribose 
• 130144-85-3 (2R,3S,5S)-2-tert-butyldiphenylsilanyloxymethyl-3-hydroxy-5α-methoxytetrahydrofuran 
• 874-60-2 4-methyl-benzoyl chloride 
• 78137-90-3 methyl 2-deoxy-3-O-(p-toluoyl)-α-D-ribofuranoside 
• 201853-69-2 4-Methyl-benzoic acid (2R,3S,5S)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-methoxy-tetrahydro-furan-3-yl ester 

Downstream Products

• 201853-78-3 4-Methyl-benzoic acid (2S,3S,5S)-5-(2,6-dichloro-purin-9-yl)-2-methylcarbamoyl-tetrahydro-furan-3-yl ester 
• 201853-77-2 4-Methyl-benzoic acid (2S,3S,5R)-5-(2,6-dichloro-purin-9-yl)-2-methylcarbamoyl-tetrahydro-furan-3-yl ester 
• 201853-75-0 methyl 2-deoxy-N-methyl-3-O-(p-toluoyl)-α-D-ribofuranosiduronamide 

Relevant academic research and scientific papers

Synthesis of New Nucleosides by Coupling of Chloropurines with 2- and 3-Deoxy Derivatives of N-Methyl-D-ribofuranuronamide

The synthesis of new deoxyribose nucleosides by coupling chloropurines with modified D-ribose derivatives is reported. The methyl 2-deoxy-N-methyl-3-O-(p-toluoyl)-α-D-ribofuranosiduronamide (α-D-8) and the corresponding anomer β-D-8 were synthesized start