85372-12-9

Upstream product

• 100-27-6 2-(4-nitrophenyl)ethanol 
• 58-63-9 Inosine 
• 53676-18-9 2,5-dichlorophenyl phosphorodichloridate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 85363-64-0 9-{(2R,3R,4S,5R)-4-(tert-Butyl-dimethyl-silanyloxy)-3-hydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-1,9-dihydro-purin-6-one 
• 69659-63-8 5'-O-(4-methoxytrityl)inosine 
• 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 

Downstream Products

• 85372-14-1 C₇₄H₈₄Cl₂N₁₀O₂₀P₂Si₂ 

Relevant academic research and scientific papers

NUCLEOTIDES, XXXIII: SYNTHESIS AND PROPERTIES OF INOSINATE TRIMER I2'p5'I2'p5'I AND INOSINATE TETRAMER I2'p5'I2'p5'I2'p5'I.

The chemical synthesis of 2'-5'-inosinate trimer and tetramer was achieved by the phosphotriester method using the 2-(p-nitrophenyl)ethyl group for phosphate protection.The sugar hydroxyl groups have either been protected by the (tert-butyl)dimethylsilyl

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.