220643-49-2

Upstream product

• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 220643-48-1 6-[1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-hex-5-ynoic acid 4,5-dimethoxy-2-nitro-benzyl ester 
• 928-90-5 5-hexyl-1-ol 
• 148134-86-5 2'-deoxy-3',5'-bis(O-tert-butyldimethylsilyl)-5-iodouridine 
• 220643-47-0 6-{1-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl}-hex-5-ynoic acid 4,5-dimethoxy-2-nitro-benzyl ester 
• 220643-46-9 6-{1-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl}-hex-5-ynoic acid 
• 220643-38-9 3',5'-O-bis(tert-butyldimethylsilyl)-2'-deoxy-5-(6-hydroxyhex-1-ynyl)uridine 

Relevant academic research and scientific papers

Introducing structural diversity in oligonycleotides via photolabile, convertible C5-substituted nucleotides

Chemically synthesized oligonucleotides are functionalized at defined sites while in their protected form on solid-phase supports via the incorporation of nucleotides containing masked alkyl carboxylic acids or alkylamines. The reactive functional groups