24744-17-0

Upstream product

• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 31111-31-6 6-methyl-2,4-bis(trimethylsiloxy)pyrimidine 
• 626-48-2 6-Methyluracil 

Downstream Products

• 42188-33-0 2,2'-anhydro-1-(3,5-di-O-benzoyl-β-D-arabinofuranosyl)-6-methyl-2,4(1H,3H)-pyrimidinedione 
• 23316-76-9 6-methyl-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2,4(1H,3H)-pyrimidinedione 
• 25691-87-6 6-methyl-1,3-bis(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2,4-(1H,3H)-pyrimidinedione 

Relevant academic research and scientific papers

Synthesis and structure-activity relationships of uracil nucleotide derivatives and analogues as agonists at human P2Y2, P2Y4, and P2Y6 receptors

A series of UTP, UDP, and UMP derivatives and analogues were synthesized and evaluated at the human pyrimidinergic P2Y receptor subtypes P2Y2, P2Y4, and P2Y6 stably expressed in 1321N1 astrocytoma cells. Substituents at N3

Nucleoside Syntheses, XXII. Nucleoside Synthesis with Trimethylsilyl Triflate and Perchlorate as Catalysts

The novel Lewis acids (CH3)3SiOSO2CF3 (5), (CH3)3SiOSO2C4F9 (6), and (CH3)3SiClO4 (4) are highly selective and efficient Friedel-Crafts catalysts for nucleoside formation from silylated heterocycles and peracylated sugars as well as for rearrangements of persilylated protected nucleosides.With basic silylated heterocycles these new catalysts give much higher yields of the natural N-1-nucleosides than with SnCl4.