The reaction of pentacyanonitrosylferrate(II) with primary amines as a source of stabilized aliphatic diazonium ions: A new route to secondary amines
Pentacyanonitrosylferrate(II), 1, reacts with n-butylamine to produce di-n-butylamine in high yields (81-95%). The absence of rearranged products indicates that the initially produced diazonium ion is stabilized by coordination to the metal. Benzylamine and 1,4-diaminobutane react with 1 to produce...
Guardado en:
Autores principales: | Doctorovich, F., Trápani, C. |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_00404039_v40_n25_p4635_Doctorovich |
Aporte de: |
Ejemplares similares
-
The reaction of pentacyanonitrosylferrate(II) with primary amines as a source of stabilized aliphatic diazonium ions: A new route to secondary amines
Publicado: (1999) -
Stabilization of aliphatic and aromatic diazonium ions by coordination: An experimental and theoretical study
por: Doctorovich, F., et al. -
Stabilization of aliphatic and aromatic diazonium ions by coordination: An experimental and theoretical study
Publicado: (2000) -
The reaction of [Ru(bpy)2(NO)Cl]2+ and [Fe(CN)5NO]2- with benzylamine: Coordinated nitrosyl as an oxidizing agent
por: Doctorovich, Fabio Ariel, et al.
Publicado: (2001) -
The reaction of [Ru(bpy)2(NO)Cl]2+ and [Fe(CN)5NO]2- with benzylamine: Coordinated nitrosyl as an oxidizing agent
por: Doctorovich, F., et al.