669772-59-2

Upstream product

• 102691-36-1 N,N,N',N'-tetraisopropyl 2-cyanoethylphosphorodiamidite 
• 54898-05-4 N,2',3'-O-tribenzoylcytidine 
• 107526-15-8 N⁴-benzoyl-2',3'-O-dibenzoyl-5'-O-(4,4'-dimethoxytrityl)cytidine 
• 81246-76-6 4-N-benzoyl-1-(5-O-dimethoxytrityl-β-D-ribofuranosyl)cytosine 
• 98-88-4 benzoyl chloride 
• 124482-92-4 2-cyanoethyl-N,N-(diisopropylamino)chlorophosphine 

Downstream Products

• 917598-89-1 6-N-benzoyl-5'-O-[di(2-cyanoethoxy)phosphinyl]-P-(2-cyanoethyl)-1'-deoxy-2'-isoadenylyl-(3'->5')-4-N,2'-O,3'-O-tribenzoylcytidine 
• 917598-90-4 6-N-benzoyl-5'-O-[(2-cyanoethoxy)(ethoxy)phosphinyl]-P-(2-cyanoethyl)-1'-deoxy-2'-isoadenylyl-(3'->5')-4-N,2',3'-tribenzoylcytidine 
• 917598-85-7 6-N-benzoyl-P-(2-cyanoethyl)-1'-deoxy-2'-isoadenylyl-(3'->5')-4-N,2'-O,3'-O-tribenzoylcytidine 

Relevant academic research and scientific papers

Synthesis, characterization, and biological properties of small branched RNA fragments containing chiral (Rp and Sp) 2′,5′-phosphorothioate linkages

Synthetic branched RNA fragments were prepared to examine the stereochemical requirements for hydrolysis of RNA lariats by the yeast debranching enzyme (yDBR). Specifically, two branched trinucleoside diphosphates and a tetranucleoside triphosphate contai

Synthetic approaches to nuclease-resistant, nonnatural dinucleotides of anti-HIV integrase interest

□ New, nonnatural dinucleotide 5′-monophosphates with a surrogate isonucleoside component of L-related stereochemistry, have been synthesized. Structures of the target compounds were confirmed by multinuclear NMR spectra (1H, 13C, s