874889-96-0

Upstream product

• 65-46-3 CYTIDINE 
• 69304-42-3 3',5'-O-[(1,1,3,3-tetraisopropyl)-1,3-disiloxanediyl]cytidine 
• 874889-90-4 2'-O-(bis(2-acetoxyethoxy)methyl)-4-N-(4,4'-dimethoxytrityl)cytidine 
• 874889-89-1 3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)-4-N-(4,4'-dimethoxytrityl)cytidine 
• 874889-91-5 2'-O-(bis(2-acetoxyethoxy)methyl)-5'-O-[bis(trimethylsiloxy)(cyclododecyloxy)silyl]-4-N-(4,4'-dimethoxytrityl)cytidine 
• 92611-10-4 bis(N,N-diisopropylamino)methoxyphosphine 

Downstream Products

• 874889-97-1 C₉₇H₁₃₁N₆O₃₁PSi₃ 

Relevant academic research and scientific papers

Synthesis of isotopically labeled P-site substrates for the ribosomal peptidyl transferase reaction

(Chemical Equation Presented) Isotopomers of the ribosomal P-site substrate, the trinucleotide peptide conjugate CCA-pcb (Zhong, M.; Strobel, S. A. Org. Lett. 2006, 8, 55-58), have been designed and synthesized in 26-35 steps. These include individual iso

Synthesis of the ribosomal P-site substrate CCA-pcb

(Chemical Equation Presented) CCA-pcb (cytidylyl-(3′5′)- cytidylyl-(3′5′)-3′(2′)-O-(N-(6-D-(+) -biotinoylaminohexanoyl)-L-phenylalanyl)adenosine), a ribosomal P-site substrate, was synthesized by phosphoramidite chemistry in 26 steps with an overall yield