1400908-45-3

Upstream product

• 1400908-44-2 5-azido-3-O-benzyl-7-O-(tert-butyldiphenylsilyl)-5,6-dideoxy-1,2-O-isopropylidene-β-L-talo-hepto-1,4-furanose 
• 1400908-43-1 3-O-benzyl-7-O-(tert-butyldiphenylsilyl)-6-deoxy-1,2-O-isopropylidene-α-D-allo-hepto-1,4-furanose 
• 65-71-4 thymin 
• 1400908-42-0 5-O-acetyl-3-O-benzyl-7-O-(tert-butyldiphenylsilyl)-6-deoxy-1,2-O-isopropylidene-α-D-allo-hepto-1,4-furanose 
• 843674-28-2 C₁₉H₂₆O₇ 

Downstream Products

• 1400908-46-4 2'-O-acetyl-5'-azido-3'-O-benzyl-3-N-(benzyloxymethyl)-5'-C-[(S)-2-(tert-butyldiphenylsiloxy)ethyl]-5'-deoxythymidine 
• 1400908-60-2 C₆₅H₇₇N₅O₁₅Si 
• 1400908-50-0 5'-amino-3'-O-benzyl-3-N-(benzyloxymethyl)-5'-deoxy-2'-O-methyl-5'-C-[(S)-2-methoxyethyl]thymidine 
• 1400908-49-7 5'-azido-3'-O-benzyl-3-N-(benzyloxymethyl)-5'-deoxy-2'-O-methyl-5'-C-[(S)-2-methoxyethyl]thymidine 
• 1400908-48-6 5'-azido-3'-O-benzyl-3-N-(benzyloxymethyl)-5'-deoxy-5-C-[(S)-2-hydroxyethyl]thymidine 
• 1400908-47-5 5'-azido-3'-O-benzyl-3-N-(benzyloxymethyl)-5'-C-[(S)-2-(tert-butyldiphenylsiloxy)ethyl]-5'-deoxythymidine 

Relevant academic research and scientific papers

Studies toward oxyacetamide-linked RNA analogues: Synthesis and conformation of a modified dinucleoside

A new oxyacetamide-modified dinucleoside with 5-(S) chirality, a hydrophobic 5-C-(2-methoxyethyl) group, and a 2-O-methyl group was synthesized from d-glucose. This dinucleoside showed a helical structure based on CD and NMR spectroscopy. The sugar puckering at the 5 and 3 ends were found to be S'- and N'-types, respectively. These results were substantiated by ab initio density functional theory. Georg Thieme Verlag Stuttgart New York.