773133-85-0

Upstream product

• 13398-11-3 iodomethyl acetate 
• 139244-01-2 6-Chloro-9-(2'-deoxy-3',5'-di-O-p-toluyl-α-D-erythro-pentofuranosyl)purine 
• 756494-16-3 9-[2-deoxy-3,5-di-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl]-6-iodopurine 
• 13943-33-4 iodomethylbenzoate 
• 773133-86-1 6-(acetyloxymethyl)-9-(2-deoxy-3,5-di-O-(p-toluolyl)-β-D-erythro-pentofuranosyl)purine 
• 91713-46-1 6-Chloro-9-(2-deoxy-3,5-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)purine 

Downstream Products

• 865434-75-9 6-(fluoromethyl)-9-(2-deoxy-3,5-di-O-(p-toluoyl)-β-D-erythro-pentofuranosyl)purine 
• 865434-84-0 6-(iodomethyl)-9-(2-deoxy-3,5-di-O-(p-toluoyl)-β-D-erythro-pentofuranosyl)purine 
• 865434-80-6 6-(methanesulfonyloxymethyl)-9-(2-deoxy-3,5-di-O-(p-toluoyl)-β-D-erythro-pentofuranosyl)purine 
• 906482-34-6 9-(2-deoxy-3,5-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)-6-formylpurine 

Relevant academic research and scientific papers

The first synthesis and cytostatic activity of novel 6-(fluoromethyl)purine bases and nucleosides

Two alternative approaches to the synthesis of novel 6-(fluoromethyl)purine bases and nucleosides are described either by direct deoxyfluorination or by multistep functional group transformations starting from 6-(hydroxymethyl) purines. 6-(Fluoromethyl)pu

Facile and efficient synthesis of 6-(hydroxymethyl)purines

(Chemical Equation Presented) A facile and efficient methodology of the synthesis of 6-(hydroxymethyl)purine derivatives (bases and nucleosides) was developed based on Pd-catalyzed cross-coupling reactions of 6-halopurines with acyloxymethylzinc iodides f