Radical-initiated tautomerization of azoethane to acetaldehyde-ethylhydrazone; Reactivity of the CH3CHNNC2H5 radical

Miklós Görgényi, László Seres

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

The N radical centre of the stabilized CH3CHNNC2H5 radical is capable of H-abstraction from azoethane and radicals at 397-445 K. The tautomerization of azoethane to its hydrazone isomers was observed in both homogeneous and heterogeneous processes.

Original languageEnglish
Pages (from-to)6447-6448
Number of pages2
JournalTetrahedron Letters
Volume31
Issue number44
DOIs
Publication statusPublished - 1990

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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