34097-18-2

Upstream product

• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 50255-86-2 2,4-bis-trimethylsilanyloxy-pteridine 
• 35777-50-5 1,3-bis(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)lumazine 
• 487-21-8 Lumazine 

Downstream Products

• 77432-78-1 1-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)lumazin-5-oxid 
• 77432-87-2 6-Chlor-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)lumazin 
• 77432-92-9 1-(3-O-Benzoyl-β-D-ribofuranosyl)lumazin-5-oxid 

Relevant academic research and scientific papers

Fused pyrimidines. 7. Nucleosides of pyrimidopyrimidinediones and pteridinediones as potential chemotherapeutic agents

Several nucleoside derivatives of pyrimido [4,5-d]pyrimidine-2,4(1H,3H)- dione 1 and 2,4(1H,3H)-pteridinedione 2 were prepared. Treating the appropriate silylated nucleobase with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D- ribofuranose 3 in the presence of trimet

SYNTHESIS AND PROPERTIES OF 2,2'-ANHYDRO-N-3-LUMAZINE NUCLEOSIDES

The reaction of 3-β-D-ribofuranosyllumazine, and its 6,7-dimethyl and diphenyl derivatives was studied for anhydronucleoside formation with adjacent carbonyl groups of the aglycon.Various conditions led to selective 2,2'-cyclization but no products posses

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.