228243-46-7

Upstream product

• 2004-06-0 6-Chloropurine riboside 
• 98-88-4 benzoyl chloride 
• 93-97-0 benzoic acid anhydride 

Downstream Products

• 862490-67-3 [[(2R,3R,4R,5R)-5-(6-Benzylamino-purin-9-yl)-3,4-bis-triethylsilanyloxy-tetrahydro-furan-2-ylmethyl]-(2-nitro-benzenesulfonyl)-amino]-acetic acid ethyl ester 
• 862490-76-4 C₄₁H₃₇N₇O₁₁S 
• 862490-68-4 {[(2R,3R,4R,5R)-5-(6-Benzylamino-purin-9-yl)-3,4-bis-triethylsilanyloxy-tetrahydro-furan-2-ylmethyl]-amino}-acetic acid ethyl ester 
• 862490-69-5 2-{[(2R,3R,4R,5R)-5-(6-Benzylamino-purin-9-yl)-3,4-bis-triethylsilanyloxy-tetrahydro-furan-2-ylmethyl]-amino}-ethanol 
• 862490-70-8 N₆-benzyl-5'-aziridino-5'-deoxy-2',3'-bis(O-triethylsilyl)adenosine 

Relevant academic research and scientific papers

Introduction of a benzoyl group onto riboside in aqueous solution: One- step synthesis of 6-chloropurine 2',3'-di-O-benzoylriboside

A benzoyl group was introduced onto the 3'-hydroxyl group of 6- chloropurine riboside by treatment with benzoylating agents in the presence of an organic or inorganic base in aqueous solution, in which further reaction gave 6-chloropurine 2',3'-di-O-benzo

o-nitrobenzenesulfonamides in nucleoside synthesis: Efficient 5′-aziridination of adenosine

5′-Aziridinoadenylates of the form 1 and a related nitrogen mustard variant have been constructed using a novel variation of the Mitsunobu reaction. Such molecules allow conversion of biological methyltransferases into nucleoside transferases, thus provid