X=Z-ZH systems as potential 1,3-dipoles. 1,5-electrocyclisatioins of imines

R. Griss*, H. Q.N. Gunaratne

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

The naphthylidene imine of methyl (1-cyclopentenyl)glycine undergoes competitive double bond isomerization and 1,5-electrocyclisation via a dipolar tautomer.

Original languageEnglish
Pages (from-to)1201-1204
Number of pages4
JournalTetrahedron Letters
Volume24
Issue number11
DOIs
Publication statusPublished - 1983

Bibliographical note

Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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