221298-14-2

Upstream product

• 221298-08-4 dimethyl 4-[5-(tert-butoxycarbonyl)amino-1-pentanoxyl]pyridine-2,6-dicarboxylate 
• 75178-90-4 N-(tert-butyloxycarbonyl)-5-aminopentanol 
• 19872-91-4 dimethyl 4-hydroxypyridine-2,6-dicarboxylate 
• 98-59-9 p-toluenesulfonyl chloride 
• 221298-12-0 4-[5-(tert-butoxycarbonyl)amino-1-pentanoxyl]pyridine-2,6-dimethanol 

Downstream Products

• 221298-18-6 14-[5-(1-pyrenecarbonyl)amino-1-pentanoxyl]-3,6,10-tris(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1⁽¹⁶⁾,12,14-triene 
• 221298-17-5 14-(5-amino-1-pentanoxyl)-3,6,10-tris(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1⁽¹⁶⁾,12,14-triene 
• 221298-16-4 14-[5-(tert-butoxycarbonyl)amino-1-pentanoxyl]-3,6,10-tris(2-nitrobenzenesulfonyl)-3,6,10,16-tetraazabicyclo[10.3.1]hexadeca-1⁽¹⁶⁾,12,14-triene 

Relevant academic research and scientific papers

Synthesis of polyazacyclophane-intercalator conjugates for combinatorial chemistry and RNA interaction studies

Anthraquinone and pyrene intercalators were conjugated to different positions of several polyazapyridinocyclophanes by various linkers to provide thirteen new polyazacyclophane-intercalator conjugates 1-13. These resulting conjugates contain two or three constrained secondary nitrogen atoms on the ring, which may serve as nucleophilic, coordinating or hydrogen-bonding sites for combinatorial, RNA interaction and coordination studies.