140701-68-4

Upstream product

• 58-63-9 Inosine 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 69659-63-8 5'-O-(4-methoxytrityl)inosine 
• 124-63-0 methanesulfonyl chloride 
• 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 

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 
• 140679-81-8 9-<3-deoxy-5-O-(4-methoxytrityl)-2-O-methylsulfonyl-β-D-threo-pentofuranosyl>hypoxanthine 
• 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 

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