Unusual dealkylations and rearrangements in aromatic nucleophilic substitution
The reaction of 2,4-dinitrohalobenzenes with di-isopropylamine produces mainly N-(2,4-dinitrophenyl)-isopropylamine and N-(2,4-dinitrophenyl)-n-propylamine instead of the expected straightforward substitution product. Dealkylations are also observed in the reactions with isopropylcyclohexylamine and...
        Guardado en:
      
    
                  
      | Autor principal: | Socolovsky, Susana Emilia | 
|---|---|
| Publicado: | 1980 | 
| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00404039_v21_n35_p3331_Nudelman http://hdl.handle.net/20.500.12110/paper_00404039_v21_n35_p3331_Nudelman | 
| Aporte de: | 
Ejemplares similares
- 
                
        
          Unusual dealkylations and rearrangements in aromatic nucleophilic substitution        
                  
 por: Nudelman, N.S., et al.
- 
                
        
          Unusual dealkylations and rearrangements in aromatic nucleophilic substitution        
                  
 por: Nudelman, N.S
 Publicado: (1980)
- 
                
        
          Evidence for A “Dimer” Nucleophile in Aromatic Nucleophilic Substitution        
                  
 por: Sbarbati Nudelman, N., et al.
- 
                
        
          Evidence for A “Dimer” Nucleophile in Aromatic Nucleophilic Substitution        
                          
 Publicado: (1982)
- 
                
        
          Evidence for A “Dimer” Nucleophile in Aromatic Nucleophilic Substitution        
                  
 por: Sbarbati Nudelman, N.
 Publicado: (1982)