476667-23-9

Upstream product

• 601-89-8 2-nitroresorcinol 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 3163-15-3 2-aminoresorcinol 
• 476667-22-8 tert-butyl 4-(1′,2′,4′-triazol-1′-yl)-5-bromocytosin-1-ylacetate 
• 476667-21-7 (5-bromo-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)acetic acid tert-butyl ester 

Downstream Products

• 476454-43-0 [8-(2-benzyloxycarbonylamino-ethoxy)-2-oxo-2,9-dihydro-10-oxa-1,3,9-triaza-anthracen-3-yl]-acetic acid 
• 476667-29-5 C₅₄H₅₄N₈O₁₂ 
• 476667-28-4 {{[8-(2-benzyloxycarbonylamino-ethoxy)-2-oxo-2,9-dihydro-10-oxa-1,3,9-triaza-anthracen-3-yl]-acetyl}-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-ethyl]-amino}-acetic acid tert-butyl ester 
• 476667-26-2 C₃₅H₃₆N₆O₉ 
• 476667-27-3 C₃₁H₂₈N₆O₉ 
• 476667-25-1 [8-(2-benzyloxycarbonylamino-ethoxy)-2-oxo-2,9-dihydro-10-oxa-1,3,9-triaza-anthracen-3-yl]-acetic acid tert-butyl ester 

Relevant academic research and scientific papers

Binding affinities of oligonucleotides and PNAs containing phenoxazine and G-clamp cytosine analogues are unusually sequence-dependent

(Chemical Equation Presented) Melting temperatures of DNA duplexes containing the phenoxazine (P) and G-clamp (X) cytosine analogues exhibited a strong and unusual dependence on the nucleoside flanking the modified nucleobase, and the same trend was obser

Synthesis of amino- and guanidino-G-clamp PNA monomers

(matrix presented) Syntheses of the protected amino- and guanidino-G-clamp PNA monomers, 9a and 9b, respectively, have been accomplished in eight steps from 5-bromouracil. Enhanced stacking interactions and additional hydrogen bonds with guanine should in