356038-34-1

Upstream product

• 98-88-4 benzoyl chloride 
• 356038-30-7 1-(2-deoxy-β-D-erythro-pentofuranosyl)-3-iodo-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine 
• 203180-17-0 1-(2-deoxy-β-D-erythro-pentofuranosyl)-3-iodo-4-isopropoxy-1H-pyrazolo[3,4-d]pyrimidin-6-amine 

Downstream Products

• 356038-37-4 N⁴,N⁶-dibenzoyl-1-[2-deoxy-5-O-(4,4'-dimethoxytrityl)-β-D-erythro-pentofuranosyl]-3-iodo-1H-pyrazolo[3,4-d]pyrimidine-4,6-diamine 

Relevant academic research and scientific papers

Nucleic acid binding compounds containing pyrazolo[3,4-d]pyrimidine analogues of purin-2,6-diamine and their uses

The present invention is in the field of nucleic acid binding compounds comprising 7-substituted 7-deaza-8aza-2,6-diamino-purine bases, compounds useful for the preparation of such compounds, various uses thereof and methods for the determination of nucle

Major-groove-halogenated DNA: The effects of bromo and iodo substituents replacing H-C(7) of 8-Aza-7-deazapurine-2,6-diamine or H-C(5) of uracil residues

Oligonucleotides containing halogenated 'purine' and pyrimidine bases were synthesized. Bromo and iodo substituents were introduced at the 7-position of 8-aza-7-deazapurine-2,6-diamine (see 2b,c) or at the 5-position of uracil residues (see 3b,c). Phospho