623145-39-1

Upstream product

• 2576-47-8 2-bromoethylamine hydrobromide 
• 5437-45-6 Benzyl bromoacetate 

Downstream Products

• 1243539-93-6 C₂₂H₂₇N₇O₆ 
• 1243539-92-5 C₂₃H₂₇N₉O₆ 
• 1243539-91-4 C₂₃H₂₇N₉O₅ 
• 623145-48-2 benzyl N-(2-azidoethyl)-N-[6-N-(benzhydryloxycarbonyl)adenine-9-acetyl]glycinate 
• 623145-46-0 benzyl N-(2-azidoethyl)-N-[4-N-(benzhydryloxycarbonyl)cytosine-1-acetyl]glycinate 
• 623145-50-6 benzyl N-(2-azidoethyl)-N-[2-N-(benzhydryloxycarbonyl)guanine-9-acetyl]glycinate 
• 623145-44-8 benzyl N-(2-azidoethyl)-N-(thymine-1-acetyl)glycinate 

Relevant academic research and scientific papers

Clickable peptide nucleic acids (cPNA) with tunable affinity

Peptide nucleic acids (PNAs) are functional analogues of natural oligonucleotides. Herein, we report the synthesis of PNAs bearing a triazole in lieu of the amide bond assembled using a "click" cycloaddition, their hybridization properties as well as the DNA-templated coupling of the azide and alkyne PNA fragments. The Royal Society of Chemistry 2010.

Azidopeptide Nucleic Acid. An Alternative Strategy for Solid-Phase Peptide Nucleic Acid (PNA) Synthesis

(Equation presented) A practical and efficient method for PNA synthesis using an azide group to mask the N-terminus is reported. The deprotection was carried out in 5 min, while couplings were complete within 60 min. The near neutral conditions of the pho