756494-16-3

Upstream product

• 3056-12-0 2-deoxy-3,5-di-O-(p-toluoyl)-α-D-erythropentofuranosyl chloride 
• 2545-26-8 6-iodopurine 
• 756494-13-0 2'-deoxy-3',5'-di-O-(4-methylbenzoyl)inosine 
• 874-60-2 4-methyl-benzoyl chloride 
• 890-38-0 2-deoxyinosine 
• 91713-46-1 6-Chloro-9-(2-deoxy-3,5-di-O-p-toluoyl-β-D-erythro-pentofuranosyl)purine 

Downstream Products

• 807626-41-1 benzyl (S)-3-[9-(3,5-di-O-p-toluoyl-2-deoxy-β-D-erythro-pentofuranosyl)purin-6-yl]-2-[(benzyloxycarbonyl)amino]propanoate 
• 1033893-68-3 9,9'-bis(3,5-di-O-p-toluoyl-2-deoxy-β-D-ribofuranosyl)-9H,9'H-[6,6']bipurinyl 
• 807626-45-5 (S)-3-[9-(2-deoxy-β-D-erythro-pentofuranosyl)purin-6-yl]-2-[(benzyloxycarbonyl)amino]propanoic acid 
• 807626-43-3 3-[9-(2-deoxy-β-D-erythro-pentofuranosyl)purin-6-yl]-2-[(benzyloxycarbonyl)amino]propanoic acid 
• 773133-81-6 6-(benzoyloxymethyl)-9-(2-deoxy-3,5-di-O-toluoyl-β-D-erythro-pentofuranosyl)purine 
• 773133-85-0 6-(hydroxymethyl)-9-(2-deoxy-3,5-di-O-(p-toluolyl)-β-D-erythro-pentofuranosyl)purine 
• 773133-74-7 6-(pivaloyloxymethyl)-9-(2-deoxy-3,5-di-O-toluoyl-β-D-erythro-pentofuranosyl)purine 
• 773133-86-1 6-(acetyloxymethyl)-9-(2-deoxy-3,5-di-O-(p-toluolyl)-β-D-erythro-pentofuranosyl)purine 
• 868071-65-2 benzyl (S)-3-{4-[9-(3,5-di-O-(p-toluoyl)-2-deoxy-β-D-erythro-pentofuranosyl)purin-6-yl]phenyl}-2-[(benzyloxycarbonyl)amino]propanoate 
• 852677-23-7 bis{9-[2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl]purin-6-yl}ethyne 
• 787550-85-0 benzyl 3-[9-(3,5-di-O-p-toluoyl-2-deoxy-β-D-erythro-pentofuranosyl)purin-6-yl]-2-[(benzyloxycarbonyl)amino]propanoate 
• 868071-79-8 (S)-3-{4-[9-(2-deoxy-β-D-erythro-pentofuranosyl)purin-6-yl]phenyl}-2-[(benzyloxycarbonyl)amino]propanoic acid 

Relevant academic research and scientific papers

SNAr iodination of 6-chloropurine nucleosides: Aromatic finkelstein reactions at temperatures below -40°C1

(Equation Presented) Mesitoyl or toluoyl esters of inosine and 2′-deoxyinosine were deoxychlorinated at C6 to give the crystalline 6-chloropurine nucleoside derivatives, which underwent quantitative conversion to the 6-iodo analogues with Nal/TFA/butanone

(PURIN-6-YL) AMINO ACID AND PRODUCTION METHOD THEREOF

The invention provides a synthetic method of (purin-6-yl)amino acids which are useful as medicaments of anticancer, anti-virus agents and so on or their intermediates. Methyl (R, S)-3-[4-(9-benzylpurin-6-yl) phenyl]-2-[ (t-butoxycarbonyl) amino] propanoat

A facile and efficient synthesis of (purin-6-yl)alanines

(Purin-6-yl)alanines, a new class of amino acid-nucleobase conjugates, were synthesized by palladium-catalyzed cross-coupling reactions of protected iodozincalanines with 6-iodopurines (9-Bn-6-iodopurine and 9-THP-6-iodopurine as well as acyl-protected 6-