153527-33-4

Upstream product

• 153527-32-3 1-(2,4-dinitrophenyl)-imidazole 4-acetic acid N-hydroxysuccinimide ester 
• 153527-30-1 2-(2-Amino-ethylamino)-9-{(2R,4S,5R)-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-1,9-dihydro-purin-6-one 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 153527-29-8 (2R,3S,5R)-5-{2-(2-Amino-ethylamino)-6-[2-(4-nitro-phenyl)-ethoxy]-purin-9-yl}-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol 
• 153527-28-7 5'-O-(4,4'-Dimethoxytrityl)-6-O-[2-(4-nitrophenyl)ethyl]-2'-deoxy-2-fluoroinosine 
• 70-34-8 2,4-Dinitrofluorobenzene 
• 645-65-8 2-(1H-imidazol-4-yl)acetic acid 
• 153527-35-6 N-(2-{9-{(2R,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-yl}-6-[2-(4-nitro-phenyl)-ethoxy]-9H-purin-2-ylamino}-ethyl)-2-[1-(2,4-dinitro-phenyl)-1H-imidazol-4-yl]-acetamide 
• 153527-31-2 [1-(2,4-dinitrophenyl)-1H-imidazol-4-yl]acetic acid 
• 132183-39-2 2-fluoro-O⁶-(2-(p-nitrophenyl)ethyl)-2'-deoxyinosine 

Relevant academic research and scientific papers

Synthesis of oligonucleotides containing N2-2-(imidazol-4-ylacetamido)ethyll-2′-deoxyguanosine

Synthesis of 2′-deoxyguanosine tethered through N-2 to an imidazole is described. The modified 2′-deoxyguanosine was converted to two different phosphoramidites, one with and the other without a 6-O-protecting group. The phosphoramidites were incorporated