1421767-16-9

Upstream product

• 1421767-15-8 1-((2R,3R,4S,5R)-3-(azidomethyl)-4-hydroxy-5-(((4-methoxyphenyl)diphenylmethoxy)methyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione 
• 1421767-14-7 ((2R,3R,4S,5R)-2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-hydroxy-5-(((4-methoxyphenyl)diphenylmethoxy)methyl)-tetrahydrofuran-3-yl)methyl 4-methylbenzenesulfonate 
• 1421767-11-4 1-((2R,3R,4S,5R)-4-Hydroxy-3-(hydroxymethyl)-5-(((4-methoxyphenyl)diphenylmethoxy)methyl)-tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione 
• 1421767-13-6 C₃₀H₂₈N₂O₇ 

Downstream Products

• 1421767-18-1 N-((2R,3R,4S,5R)-2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-O-(2-thiono-1,3,2-dithiaphospholan-5-(((4-methoxyphenyl)diphenylmethoxy)methyl)-tetrahydrofuran-3-yl)methyl)-2,2,2-trifluoroacetamide 
• 1421767-20-5 C₄₂H₄₄N₅O₁₂PS₂ 

Relevant academic research and scientific papers

Synthesis of a nucleoside phosphorodithioate analogue responsive to microenvironmental changes through chiral induction

We have synthesized a 2′-aminomethyl branched-chain sugar nucleoside phosphorodithioate from 2,2′-anhydro uridine and subjected the material to a subsequent cyclization reaction under aqueous conditions using bi-functional linkers. The rate of the cycliza