125944-20-9

Upstream product

• 98-88-4 benzoyl chloride 
• 13276-53-4 9-(2'-deoxy-β-D-threo-ribofuranosyl)-adenine 
• 139260-81-4 N-[9-[(2R,4R,5R)-5-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-4-hydroxytetrahydrofuran-2-yl]purin-6-yl]benzamide 
• 116597-14-9 N⁶-benzoyl-9-(3-O-benzoyl-2-deoxy-β-D-threo-pentofuranosyl)adenine 
• 4546-72-9 N₆-benzoyl-2'-deoxyadenosine 
• 958-09-8 2'-deoxy-D-adenosine 
• 64325-78-6 N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine 
• 606141-34-8 [(2R,3S,5R)-5-(6-benzamidopurin-9-yl)-2-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]tetrahydrofuran-3-yl] 4-nitrobenzoate 

Downstream Products

• 606141-35-9 N⁶-benzoyl-9-(3',5'-di-O-methylsulfonyl-2'-deoxy-β-D-threo-pentofuranosyl)adenine 
• 834916-60-8 N⁶-benzoyl-S,S'-diacetyl-3',5'-dithio-2'-deoxyadenosine 
• 139290-39-4 N⁶-benzoyl-9-(2'-deoxy-5'-O-(4,4'-dimethoxytrityl)-β-D-threo-pentofuranosyl)adenine 3'-(triethylammonium phosphonate) 
• 357399-11-2 C₅₃H₄₆N₈O₅S 
• 125943-99-9 N⁶-benzoyl-3',5'-diazido-2',3',5'-trideoxyadenosine 
• 357399-10-1 N⁶-benzoyl-3',5'-diamino-2',3',5'-trideoxyadenosine 
• 934980-58-2 N⁶-benzoyl-5'-(4,4'-dimethoxytrityl)-3'-S-benzoyl-2',3'-dideoxy-3'-thioadenosine 
• 148551-15-9 N⁶-benzoyl-3'-S-benzoyl-2',3'-dideoxy-3'-thioadenosine 
• 934980-56-0 [(2R,3R,5R)-5-(6-benzamidopurin-9-yl)-2-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]tetrahydrofuran-3-yl] methanesulfonate 
• 139260-81-4 N-[9-[(2R,4R,5R)-5-[[bis(4-methoxyphenyl)phenylmethoxy]methyl]-4-hydroxytetrahydrofuran-2-yl]purin-6-yl]benzamide 

Relevant academic research and scientific papers

Deoxynucleic guanidine: Synthesis and incorporation of purine nucleosides into positively charged DNG oligonucleotides

The synthesis of purine nucleosides capable of making the guanidinium linkage is described for the first time starting from the corresponding 2′-deoxynucleosides. The positively charged mixed base DNG oligomer containing guanine was synthesized on solid-p

Study on disulfur-backboned nucleic acid: Part 1, efficient synthesis of 3′,5′-dithio-2′-deoxyadenosine

An efficient procedure is established to synthesize 3′,5′- dithio-2′-deoxyadenosine starting from 2′-deoxyadenosine in five steps in 33% overall yield. In this procedure, the key intermediate 9 was synthesized by twice SN2 reactions with twice

Novel and efficient syntheses of 3′,5′-diamino derivatives of 2′,3′,5′-trideoxycytidine and 2′,3′,5′-trideoxyadenosine. Protonation behavior of 3′,5′-diaminonucleosides

High yielding synthetic routes to 3′,5′-diamino-2′,3′,5′-trideoxycytidine and 3′,5′-diamino-2′,3′,5′-trideoxyadenosine are described. In addition, the protonation behavior of 3′,5′-diamino-2′,3′,5′-trideoxycytidine, 3′,5′-diamino-2′,3′,5′-trideoxyadenosin

9-(2'-Deoxy-β-D-xylofuranosyl)adenine Building Blocks for Solid-Phase Synthesis and Properties of Oligo(2'-deoxy-xylonucleotides)

The 9-(2'-deoxy-β-D-threo-pentofuranosyl)adenine (=9-(2'-deoxy-β-D-xylofuranosyl)adenine, xAd; 2) was protected at its 6-NH2 group with either a benzoyl (5a) or a (dimethylamino)methylidene (6a) residue and with a dimethoxytrityl group at 5'-OH