Pyridinium N-heteroarylaminides: synthesis of N-heteroaryltetramines based on 1,6-bis(phenoxy)hexane and 1,3-bis(phenoxymethyl)benzene

The synthesis of a set of new N-heteroaryltetramines is reported. A regioselective alkylation on the N-exo nitrogen of pyridinium N-(heteroaryl)aminide with the corresponding tetrabromo compounds, followed by a clean N–N bond reduction of the corresponding tetra-salts, allowed an easy and general me...

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Detalles Bibliográficos
Autores: Castillo Romero, Rafael|||0000-0003-1957-3098, Izquierdo Ceinos, María Luisa, Álvarez-Builla Gómez, Julio
Tipo de recurso: artículo
Fecha de publicación:2007
País:España
Institución:Universidad de Alcalá (UAH)
Repositorio:e_Buah Biblioteca Digital Universidad de Alcalá
Idioma:inglés
OAI Identifier:oai:ebuah.uah.es:10017/2689
Acceso en línea:http://hdl.handle.net/10017/2689
https://dx.doi.org/10.1016/j.tetlet.2007.06.044
Access Level:acceso abierto
Palabra clave:Regioselective synthesis
Molecular recognition
Polyamine analogs
Ligands
Complexes
2-Aminopyridines
Derivatives
Receptors
Chemistry
N-(2'-azinyl)aminides
Chemistry, Organic
Bioquímica
Ciencia
Biochemistry
Science
Descripción
Sumario:The synthesis of a set of new N-heteroaryltetramines is reported. A regioselective alkylation on the N-exo nitrogen of pyridinium N-(heteroaryl)aminide with the corresponding tetrabromo compounds, followed by a clean N–N bond reduction of the corresponding tetra-salts, allowed an easy and general method to obtain N,N′,N″,N‴-tetrakis(2-heteroaryl)tetramines.