2-Alkyl sbstitued phenazines are obtained from phenazine and long chain alkyl N-chloroamines in conc. sulfuric acid under the condition of Hofmann-Loffler-Frytag reaction and from phenazione an aliphatic substrate and N,N-dialkyl-N-chloroamines in conc. sulfuric acid. Under these conditions the reactive species was the diprotonated form of phenazine (pKa2 = -5.1).

Alkylation of phenazine with N-chloroamines

Citterio, A.;
1978-01-01

Abstract

2-Alkyl sbstitued phenazines are obtained from phenazine and long chain alkyl N-chloroamines in conc. sulfuric acid under the condition of Hofmann-Loffler-Frytag reaction and from phenazione an aliphatic substrate and N,N-dialkyl-N-chloroamines in conc. sulfuric acid. Under these conditions the reactive species was the diprotonated form of phenazine (pKa2 = -5.1).
1978
Organic Chemistry, Free Radicals, Hetroaromatic bases, Alkylation, N-Chloroamines
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/1047385
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? ND
social impact