164576-88-9

Upstream product

• 4330-21-6 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride 

Downstream Products

• 159277-49-3 1',2'-Dideoxy-1'-(1,2,4-trimethylphenyl)-3',5'-di-O-toluoyl-β-D-ribofuranose 
• 159277-45-9 1',2'-Dideoxy-1'-(1,2,4-trimethylphenyl)-β-D-ribofuranose 
• 162517-33-1 1',2'-dideoxy-5'-O-(4,4'-dimethoxytrityl)-1'-(1,2,4-trimethylphenyl)-β-D-ribofuranose 

Relevant academic research and scientific papers

NOVEL NUCLEOSIDE ANALOGS WITH POLYCYCLIC AROMATIC GROUPS ATTACHED, METHODS OF SYNTHESIS AND USES THEREFOR

The present invention provides fluorescent nucleosides carrying polycyclic aromatic hydrocarbons such as anthracene, phenanthrene, pyrene, stilbene, tetracene or pentacene. The subject nucleosides may be synthesized using a C-glycosidic bond formation met

Naphthalene, phenanthrene, and pyrene as DNA base analogues: Synthesis, structure, and fluorescence in DNA

We describe the synthesis, structures, and DNA incorporation of deoxyribonucleosides carrying polycyclic aromatic hydrocarbons as the DNA 'base' analogue. The new polycyclic compounds are 1-naphthyl, 2-naphthyl, 9-phenanthrenyl, and 1-pyrenyl deoxynucleos

An efficient method for the synthesis of aromatic C-nucleosides

Reaction of diarylcadmium or diarylzinc reagents with 1,2-dideoxy-3,5-di-O-p-toluoyl-1-chloro-α-D-ribofuranose affords 3,5-di-O-protected aromatic C-nucleosides in good yields.