131853-35-5

Upstream product

• 56183-63-2 bis(diisopropylamino)chlorophosphine 
• 102573-69-3 5'-O-(4-4'-dimethoxytrityl)-N³-benzoyl thymidine 

Downstream Products

• 131853-36-6 C₆₈H₇₀N₅O₁₅P 
• 131853-37-7 C₆₂H₅₇N₄O₁₆P 
• 131853-67-3 C₆₂H₅₇N₄O₁₇P*C₆H₁₅N 
• 149411-89-2 C₆₂H₆₉N₅O₁₇P₂ 
• 149376-13-6 N³-Benzoylthymidin-3'-yl N,N-diisopropylphosphonamidate 
• 131853-65-1 C₄₄H₄₉ClN₃O₈P 

Relevant academic research and scientific papers

Nucleoside 3'-N,N-Dialkylphosphonamidates as Novel Nucleotide Units for the Solution-Phase Oligonucleotide Syntheis

Nucleoside 3'-N,N-diisopropylphosphonamidate building blocks for oligonucleotide syntheis were prepared in high yields from appropriately protected nucleosides by use of chlorobis(N,N-diisopropylamino)phosphine as a phosphitylating reagent.The 5'-dimethox

Nucleoside 3'-N,N-dialkylphosphonamidates: Novel building blocks for oligonucleotide synthesis

Nucleoside 3'-N,N-diisopropylphosphonamidates reacted with tris(2,4,6-tribromophenoxy)dichlorophosphorane (BDCP) to generate the corresponding aminophosphorochloridites without cleavage of the P-N bond. The reaction was applied to internucleotidic bond formation.