167147-37-7

Upstream product

• 84416-84-2 [5'-O-(4,4'-dimethoxytrityl)-N₂-isobutyryl-2'-deoxyguanosine-3'-yl]-(N,N'-diisopropyl)methylphosphoramidite 
• 108-95-2 phenol 
• 1360780-30-8 methylphenyl N₂-isobutyryl-2'-deoxy-5'-O-dimethoxytritylguanosine-3'-monophosphate 

Downstream Products

• 1360780-29-5 phenyl 2'-deoxyguanosine-3'-monophosphate 
• 1360780-31-9 phenyl-N₂-isobutyryl-2'-deoxyguanosine-3'-monophosphate 

Relevant academic research and scientific papers

Solution-phase synthesis of branched DNA hybrids based on dimer phosphoramidites and phenolic or nucleosidic cores

Branched oligonucleotides with CG zippers as DNA arms assemble into materials from micromolar solutions. Their synthesis has been complicated by low yields in solid-phase syntheses. Here we present a solution-phase synthesis based on phosphoramidites of dimers and phenolic cores that produces six-arm or four-arm hybrids in up to 61% yield. On the level of hybrids, only the final product has to be purified by precipitation or chromatography. A total of five different hybrids were prepared via the solution-phase route, including new hybrid (TCG)4TTPA with a tetrakis(triazolylphenyl)adamantane core and trimer DNA arms. The new method is more readily scaled up than solid-phase syntheses, uses no more than 4 equiv of phosphoramidite per phenolic alcohol, and provides routine access to novel materials that assemble via predictable base-pairing interactions.