402859-69-2

Upstream product

• 402859-68-1 2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)1-hydroxybenzene 
• 98-88-4 benzoyl chloride 
• 288864-01-7 2-allyloxyphenylmagnesium iodide 
• 223590-99-6 (2S,3S,4S)-3-benzyloxy-4-benzyloxymethyl-2-hydroxymethyl-4-hydroxytetrahydrofuran 
• 402859-66-9 1-allyloxy-2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)benzene 

Downstream Products

• 402859-70-5 1-benzoyloxy-2-(2-O,4-C-methylene-β-D-ribofuranosyl)benzene 
• 402859-71-6 1-benzoyloxy-2-[5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl]benzene 
• 1445870-48-3 1-benzoyloxy-2-{3-O-[2-cyanoethoxy(diisopropylamino)phosphino]-5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl}benzene 
• 402859-72-7 2-[5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-b-D-ribofuranosyl]-1-hydroxybenzene 
• 402859-73-8 1-allyloxy-2-[5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl]benzene 
• 402859-74-9 1-allyloxy-2-{3-O-[2-cyanoethoxy(diisopropylamino)phosphino]-5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl}benzene 

Relevant academic research and scientific papers

Base-pair recognition ability of hydroxyphenyl nucleobases in parallel triplex DNA

Oligonucleotides containing 2′-deoxyribonucleotides bearing hydroxyphenyl nucleobases or their 2′,4′-BNA-modified analogs were synthesized, and the triplex-forming ability of their oligonucleotides with double-stranded DNA targets was evaluated by UV melt

NOVEL NUCLEOSIDE ANALOGS AND OLIGONUCLEOTIDE DERIVATIVES CONTAINING THESE ANALOGS

Nucleoside analogues expressed by the following general formula ???where B represents an aromatic base having carbonyl oxygen at the 2-position, or a 2-hydroxyphenyl group, or oligonucleotide derivatives containing one or more of the nucleoside analogues