109923-79-7

Upstream product

• 3080-30-6 1-O-acetyl-2,3,5-tri-O-benzoyl-β-L-ribofuranose 
• 41546-19-4 α-L-lyxose 
• 66224-66-6 adenine 
• 4005-49-6 N-benzoyladenine 
• 18055-47-5 N-Benzoyl-N,9-bis(trimethylsilyl)adenin 
• 109923-78-6 6-N-benzoyl-2',3',5'-tri-O-benzoyl-β-L-adenosine 
• 20074-49-1 β-L-arabinofuranoside 
• 93-97-0 benzoic acid anhydride 
• 69304-37-6 1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane 
• 868663-26-7 N⁶-benzoyl-β-L-adenosine 

Downstream Products

• 868663-28-9 5'-O-(4,4'-dimethoxytrityl)-2'-O-tetrahydrofuran-2-yl-N⁶-benzoyl-L-adenosine 
• 868663-27-8 2'-O-tetrahydrofuran-2-yl-N⁶-benzoyl-L-adenosine 

Relevant academic research and scientific papers

Synthesis and structural characterization of diastereomeric isomers of RNA trimer adenylyl(3′-5′)adenylyl(3′-5′)adenosine

We have synthesized the diastereomeric isomers of adenylyl(3′- 5′)adenylyl(3′-5′)adenosine (ApApA), and investigated their helical structures and hybridization properties with d-poly(U) by circular dichroism (CD) and UV melting experiments. The configurat

Synthesis of the mirror image of the RNA fragment D-CAAGG: A model compound to study interactions between oligonucleotides of opposite handedness

The pentamer L-CAAGG was prepared starting from properly protected β-L-ribonucleosides via a phosphotriester approach.The identity and chiral purity of the pentamer were established by 1H NMR and CD spectroscopy, respectively.