207232-08-4

Upstream product

• 100-39-0 benzyl bromide 
• 406212-27-9 (4aS,7S,7aS)-6-methoxy-2,2-dimethyltetrahydro-4H-furo[3,2-d][1,3]dioxin-7-ol 
• 91-09-8 methyl α,β-L-xyloside 
• 87-72-9 L-xylopyranose 

Downstream Products

• 207232-09-5 methyl 2-O-benzyl-α,β-L-xylofuranoside 
• 207232-19-7 (2R,4R)-3-benzoyl-1-(2-tert-butyldiphenylsilyloxymethyl-3-methylene-tetrahydrofuran-4-yl)-1H-pyrimidine-2,4-dione 
• 207232-16-4 (2R,4R)-2-amino-6-chloro-9-(2-tert-butyldiphenylsilyloxymethyl-3-methylene-tetrahydrofuran-4-yl)-9H-purine 
• 207232-15-3 (2R,4R)-6-chloro-9-(2-tert-butyldiphenylsilyloxymethyl-3-methylene-tetrahydrofuran-4-yl)-9H-purine 
• 207232-14-2 1,4-anhydro-5-O-(tert-butyldiphenylsilyl)-3-deoxy-3-C-methylene-L-xylitol 
• 207232-10-8 methyl 2,5-di-O-benzyl-L-xylofuranoside 
• 406211-95-8 1,4-anhydro-2,5-di-O-benzyl-L-xylofurano-3-ulose 
• 207232-12-0 1,4-anhydro-2,5-di-O-benzyl-3-deoxy-3-C-methylene-L-xylitol 
• 207232-11-9 1,4-anhydro-2,5-di-O-benzyl-L-xylitol 
• 207232-13-1 1,4-anhydro-3-deoxy-3-C-methylene-L-xylitol 
• 115260-32-7 methyl 2,5-di-O-benzyl-β-L-xylofuranoside 
• 115260-31-6 methyl 2,5-di-O-benzyl-α-L-xylofuranoside 

Relevant academic research and scientific papers

Synthesis and antiviral activity of novel isodideoxy nucleosides with exocyclic methylene

Novel isodideoxy nucleosides with exocyclic methylene were synthesized starting from L-xylose utilizing anomeric demethoxylation, Wittig reaction and Mitsunobu reaction as key steps and evaluated for antiviral activity.