1,7-Electrocyclisations of stabilised azomethine ylides

Miklós Nyerges, Andrea Virányi, Áron Pintér, László Toke

Research output: Contribution to journalArticle

24 Citations (Scopus)

Abstract

Ester-stabilised α,β:γ,δ-unsaturated azomethine ylides 9 were generated by the deprotonation method from isoquinolinium salts 8. 1,7-Electrocyclisation of these dipoles followed by a 1,5-hydrogen shift, gives tetrahydro[5,6]azepino[2,1-a]isoquinolines 10.

Original languageEnglish
Pages (from-to)793-794
Number of pages2
JournalTetrahedron Letters
Volume44
Issue number4
DOIs
Publication statusPublished - Jan 20 2003

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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