69659-63-8

Upstream product

• 58-63-9 Inosine 
• 14470-28-1 mono-4-methoxytrityl chloride 

Downstream Products

• 140679-73-8 9-{(2R,3S,5S)-3-Hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-1,9-dihydro-purin-6-one 
• 140679-78-3 9-(3-deoxy-5-O-(4-methoxytrityl)-β-D-threo-pentofuranosyl)-N¹-methylhypoxanthine 
• 140679-83-0 9-{(2R,3R,5S)-3-Azido-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-1,9-dihydro-purin-6-one 
• 140679-81-8 9-<3-deoxy-5-O-(4-methoxytrityl)-2-O-methylsulfonyl-β-D-threo-pentofuranosyl>hypoxanthine 
• 140701-68-4 5'-O-(4-methoxytrityl)-2',3'-bis-O-methylsulfonylinosine 
• 85372-11-8 Phosphoric acid (2R,3R,4R,5R)-4-(tert-butyl-dimethyl-silanyloxy)-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-2-(6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl ester 2-(4-nitro-phenyl)-ethyl ester; compound with triethyl-amine 
• 85372-09-4 Phosphoric acid (2R,3R,4R,5R)-4-(tert-butyl-dimethyl-silanyloxy)-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-2-(6-oxo-1,6-dihydro-purin-9-yl)-tetrahydro-furan-3-yl ester 2,5-dichloro-phenyl ester 2-(4-nitro-phenyl)-ethyl ester 
• 85372-13-0 C₆₈H₆₈N₉O₁₇PSi 
• 85363-68-4 C₆₆H₈₈N₉O₁₅PSi₃ 
• 85363-71-9 2'-O-(tert-butyl)dimethylsilylinosinyl<2'-P-(2-(p-nitrophenyl)ethyl)><*>5'>-2',3'-di-O-benzoylinosine 
• 85363-69-5 2'-O-(tert-butyl)dimethylsilylinosinyl-<2'-P-(2-(p-nitrophenyl)ethyl)><*>5'>-2,3'-bis-O-(tert-butyl)dimethylsilylinosine 
• 85372-12-9 3'-O-(tert-butyl)dimethylsilylinosine-2'-<2,5-dichlorophenyl 2-(p-nitrophenyl)ethyl phosphate> 
• 85363-67-3 2',3'-di-O-benzoylinosine 
• 140679-77-2 Methanesulfonic acid (2R,3R,4R,5R)-5-(1-methanesulfonyl-6-oxo-1,6-dihydro-purin-9-yl)-4-methanesulfonyloxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 

Relevant academic research and scientific papers

General Method for the Synthesis of 2'-Azido-2',3'-dideoxynucleosides by the Use of -Hydride Shift and &β-Elimination Reactions

The title nucleoside (16U, C, G and H) were synthesized from pyrimidine and purine ribonucleosides in about 30percent overall yield in 6 steps via key intermediates, protected 3'-deoxy-arabino-nucleosides, which were obtained by deoxygenative -hydrid

SYNTHESIS OF INOSINATE TRIMER I2'p5'I2'p5'I AND TETRAMER I2'p5'I2'p5'I2'p5'I

The trimeric and tetrameric inosinates with (2'-5')-linkages were synthesized via the phosphotriester approach using the p-nitrophenylethyl group for phosphate protection.