149454-69-3

Upstream product

• 144216-96-6 9-(3,4-O-isopropylidene-α-L-arabinopyranosyl)-2-N-palmitoylguanine 
• 1005-56-7 phenylcarbonochloridothioate 
• 87-72-9 L-(+)-arabinose 
• 149560-31-6 1,2-di-O-benzoyl-3,4-O-isopropylidene-L-arabinopyranose 
• 58645-35-5 3,4-O-isopropylidene-β-L-arabinopyranose 

Relevant academic research and scientific papers

Potential Antiviral Agents. Stereospecific Synthesis of Purines and Pyrimidines Substituted with Chiral Acyclic Chains by Sugar-Ring Opening of &α-L-Arabinopyranosyl Nucleosides

3',4'-Seco-nucleosides as well as their derivatives lacking C-3', all retain the carbon framework and chirality of the β-D-ribofuranosyl moiety of the nucleosides occurring in nucleic acids, have been synthesized and their antiviral properties examined.Mo