144963-47-3

Upstream product

• 380611-22-3 Methyl <1-(13)C>-D-ribofuranoside 
• 83866-07-3 1-O-methyl-D-[1-13C]ribofuranoside 
• 108-98-5 thiophenol 
• 335595-58-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-<1-13C>ribofuranoside 

Downstream Products

• 144963-48-4 C₃₆⁽¹³⁾CH₂₉N₃O₉ 
• 144970-91-2 C₃₀⁽¹³⁾CH₂₆N₂O₉ 
• 144963-61-1 C₄₇⁽¹³⁾CH₅₄N₇O₉P 
• 144963-60-0 C₄₆⁽¹³⁾CH₅₂N₇O₇P 
• 144963-59-7 C₄₅⁽¹³⁾CH₅₂N₅O₈P 
• 144963-58-6 C₃₉⁽¹³⁾CH₄₉N₄O₈P 
• 144963-53-1 C₃₅⁽¹³⁾CH₄₇N₅O₇SSi₂ 
• 144963-52-0 C₃₄⁽¹³⁾CH₄₇N₃O₈SSi₂ 
• 144963-51-9 C₂₈⁽¹³⁾CH₄₄N₂O₈SSi₂ 
• 144963-57-5 C₁₇⁽¹³⁾CH₁₉N₅O₆ 

Relevant academic research and scientific papers

Phenylsulfenyl D-Ribofuranosides as Efficient Ribosyl Donors: Application to the Synthesis of -(Deoxy)Nucleosides

Readily available phenylsulfenyl 2,3,5-tri-O-benzoyl-β-D-ribofuranoside glycosylates silylated nucleobases in a fast, high-yielding and stereoselective reaction promoted by trimethylsilyl trifluoromethanesulfonate.The method has been applied to the synthesis of labelled nucleosides further transformed to building blocks ready for oligodeoxynucleotide construction. Key words: anomeric sulfoxides; silylated nucleobases; nucleosides; 2'-deoxynucleosides.