1512860-68-2

Upstream product

• 79366-24-8 9-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-9H-purine 
• 110-82-7 cyclohexane 
• 98-89-5 Cyclohexanecarboxylic acid 

Relevant academic research and scientific papers

Synthesis of cycloalkyl substituted purine nucleosides: Via a metal-free radical route

An efficient route to synthesize cycloalkyl substituted purine nucleosides was developed. This metal-free C-H activation was accomplished by a tBuOOtBu initiated radical reaction. By adjusting the amount of tBuOOtBu and reaction time, the selective synthe

Radical route for the Alkylation of Purine Nucleosides at C6 via Minisci reaction

A highly regioselective Minisci reaction with the decarboxylative alkylation of purine nucleosides under mild conditions was developed. With 5 mol % AgNO3 as a catalyst and (NH4)2S 2O8 as an oxidant, a series of purine nucleosides including ribosyl, deoxyribosyl, arabinosyl purine nucleosides worked well with primary, secondary, and tertiary aliphatic carboxylic acids.