83373-05-1

Upstream product

• 85026-60-4 (3R,4S,5R)-4-(benzoyloxy)-5-((benzoyloxy)methyl)tetrahydrofuran-2,3-diyl diacetate 
• 66224-66-6 adenine 
• 83434-58-6 Di-O-benzoyl-3,5 di-O-acetyl-1,2 α-D-xylofurannose 

Downstream Products

• 31079-98-8 N⁶-benzoyl-9-(2,3-di-O-benzoyl-β-D-xylofuranosyl)adenine 
• 31079-97-7 O-monomethoxytrityl-5' N,O-tribenzoyl-6,2',3' β-D-xylofurannosyl-9 adenine 
• 81352-48-9 N,O-Dibenzoyl-6,3' O-monomethoxytrityl-5' β-D-xylofurannosyl-9 adenine 
• 83373-10-8 N,O-Dibenzoyl-6,3' O-monomethoxytrityl-5' O-t-butyldimethylsilyl-2' β-D-xylofurannosyl-9 adenine 
• 83373-07-3 Di-O-benzoyl-3',5' O-t-butyldimethylsilyl-2' β-D-xylofurannosyl-9 adenine 
• 31079-96-6 O-monomethoxytrityl-5' β-D-xylofurannosyl-9 adenine 
• 83373-09-5 9-<5'-O-(monomethoxytrityl)-2'-O-(tert-butyldimethylsilyl)-β-D-xylofuranosyl>adenine 
• 83373-06-2 Di-O-benzoyl-3',5' β-D-xylofurannosyl-9 adenine 

Relevant academic research and scientific papers

Systematic Synthesis and Biological Evaluation of α- and β-D-Xylofuranosyl Nucleosides of the Five Naturally Occurring Bases in Nucleic Acids and Related Analogues

The α- and β-D-xylofuranosyl analogues of the naturally occurring nucleosides, as well as other D-xylofuranosyl derivatives, have been the subject of a systematic synthesis and examination of their biological, i.e. antiviral antimetabolic, and cytostatic

Nucleosides de synthese XXII: obtention, comme synthons oligoxylonucleotidiques, de D-xylofurannosyl adenines specifiquement substitues

This work describes the synthesis of certain nucleoside synthons which are necessary in order to obtain oligoxylonucleotides.The utilization of a non-symmetrically substituted xyloside substituted at the 2-position permits one to obtain, in satisfactory y