1422959-01-0

Upstream product

• 1422958-99-3 5-amino-3-iodophthalimide 
• 1422958-85-7 3-iodo-5-nitrophthalimide 
• 1422959-00-9 5-(N-(phenoxyacetyl)amino)-3-iodophthalimide 
• 181871-82-9 {(2R,3S)-3-[(tert-butyldimethylsilyl)oxy]-2,3-dihydrofuran-2-yl}methanol 
• 1005499-46-6 3-iodo-2-methyl-5-nitrobenzoic acid 
• 1975-52-6 5-nitro-o-toluic acid 

Downstream Products

• 1422958-93-7 C₅₁H₅₅N₄O₁₀P 
• 1422958-91-5 C₄₂H₃₈N₂O₉ 
• 1422958-97-1 1-(5-(N-(phenoxyacetyl)amino)-N-(4,4'-dimethoxytrityl)phthalimid-3-yl)-3-O-[(2-cyanoethoxy)diisopropylaminophosphanyl]-5-O-(4,4'-dimethoxytrityl)-1,2-dideoxy-β-D-ribofuranose 
• 1422958-95-9 1-(5-(N-(phenoxyacetyl)amino)-N-(4,4'-dimethoxytrityl)phthalimid-3-yl)-5-O-(4,4'-dimethoxytrityl)-1,2-dideoxy-β-D-ribofuranose 
• 1422958-90-4 1-(5-(N-(phenoxyacetyl)amino)phthalimid-3-yl)-1,2-dideoxy-β-D-ribofuranose 

Relevant academic research and scientific papers

Synthesis of 4-aminophthalimide and 2,4-diaminopyrimidine C-nucleosides as isosteric fluorescent DNA base substitutes

The 4-aminophthalimide C-nucleoside 1 was designed as an isosteric DNA base surrogate, and a synthetic route to nucleoside 1 together with the 2,4-diaminopyrimidine-C-nucleoside 2 as a potential counterbase was worked out. The key steps in both synthetic