1315250-86-2

Upstream product

• 1315250-74-8 1β-(6-bromopyridin-3-yl)-1-O-acetyl-2,3,5-tri-O-(tert-butyldimethylsilyl)-D-ribofuranose 
• 1315250-75-9 1β-(6-bromopyridin-3-yl)-1-deoxy-2,3,5-tri-O-(tert-butyldimethylsilyl)-D-ribofuranose 
• 98-80-6 phenylboronic acid 
• 92512-25-9 (3R,4R,5R)-3,4-bis((tert-butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)dihydrofuran-2(3H)-one 

Downstream Products

• 1315251-02-5 1β-(6-phenylpyridin-3-yl)-1-deoxy-D-ribofuranose 

Relevant academic research and scientific papers

General and modular synthesis of isomeric 5-substituted pyridin-2-yl and 6-substituted pyridin-3-yl C-ribonucleosides bearing diverse alkyl, aryl, hetaryl, amino, carbamoyl, and hydroxy groups

A general modular and practical methodology for preparation of diverse 5-substituted pyridin-2-yl and 6-substituted pyridin-3-yl C-ribonucleosides was developed. Regioselective lithiation of 2,5-dibromopyridine proceeded at position 5 or 2 depending on th