154463-68-0

Upstream product

• 66224-66-6 adenine 
• 201287-82-3 1,2-di-O-acetyl-3,5-di-O-benzoyl-β-L-xylofuranosyle 

Downstream Products

• 216571-43-6 9-(3,5-di-O-benzoyl-β-L-xylofuranosyl)adenine 
• 14365-45-8 L-dA 
• 58-61-7 L-adenosine 
• 216571-44-7 9-(3,5-Di-O-benzoyl-2-deoxy-β-L-threo-pentofuranosyl)adenine 
• 233681-08-8 (2S,3S,5S)-2-Hydroxymethyl-5-(6-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-purin-9-yl)-tetrahydro-furan-3-ol 
• 233681-07-7 C₄₄H₃₇N₅O₆ 
• 233681-09-9 (2S,3S,5S)-2-[(4-Methoxy-phenyl)-diphenyl-methoxymethyl]-5-(6-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-purin-9-yl)-tetrahydro-furan-3-ol 
• 233681-05-5 C₃₁H₂₅N₅O₇ 
• 233681-03-3 C₃₇H₃₉N₅O₇Si 
• 258529-64-5 (2S,3R,5S)-2-[(4-Methoxy-phenyl)-diphenyl-methoxymethyl]-5-(6-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-purin-9-yl)-tetrahydro-furan-3-ol 

Relevant academic research and scientific papers

Unnatural β-L-enantiomers of nucleoside analogues as potent anti- hepatitis B virus agents

Several 2'- or 3'- substituted 2',3'-dideoxy-β-L-nucleosides bearing adenine as the base were stereospecifically synthesized and their antiviral properties examined. Two of them, namely 2'-azido- and 3'-azido-2',3'- dideoxy-β-L-adenosine (2'-N3

Synthesis and antiviral evaluation of β-L-xylo-furanosyl nucleosides of the five naturally occurring nucleic acid bases

The β-L-xylo-furanosyl analogues of the naturally occurring nucleosides have been synthesized and their antiviral properties examined. All these compounds were hitherto unknown and they were stereospecifically prepared by glycosylation of pyrimidine and p