1374985-70-2

Upstream product

• 1233209-66-9 1β-(2,4-dichloropyrimidin-5-yl)-1,2-dideoxy-2,3-didehydro-3-O-(tert-butyldimethylsilyl)-D-ribofuranose 
• 1233209-67-0 1β-(2,4-dichloropyrimidin-5-yl)-1,2,3-trideoxy-3-oxo-D-ribofuranose 
• 1233209-68-1 1β-(2,4-dichloropyrimidin-5-yl)-1,2-dideoxy-D-ribofuranose 
• 1233209-71-6 1β-(2-chloro-4-aminoyrimidin-5-yl)-1,2-dideoxy-D-ribofuranose 
• 1233209-72-7 1β-(2-chloro-4-methoxyyrimidin-5-yl)-1,2-dideoxy-D-ribofuranose 
• 1374985-48-4 1β-(4-amino-2-chloropyrimidin-5-yl)-3,5-di-O-(tert-butyldimethylsilyl)-1,2-dideoxy-D-ribofuranose 
• 98-80-6 phenylboronic acid 
• 181871-82-9 {(2R,3S)-3-[(tert-butyldimethylsilyl)oxy]-2,3-dihydrofuran-2-yl}methanol 

Downstream Products

• 1374985-71-3 1β-(4-amino-2-phenylpyrimidin-5-yl)-1,2-dideoxy-D-ribofuranose 

Relevant academic research and scientific papers

A general regioselective approach to 2,4-disubstituted pyrimidin-5-yl C-2-deoxyribonucleosides

A new modular synthesis of diverse 2,4-disubstituted pyrimidin-5-yl C-2-deoxyribonucleosides by sequential regioselective reactions of 2,6-dichloropyrimidin-5-yl C-nucleoside was developed. The intermediate was prepared by the Heck coupling of 2,6-dichlor