"Ionic" Diels-Alder reaction of hetaryldienamines

András Kotschy, György Hajós, Géza Timári, András Messmer, Joachim G. Schantl

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Hetaryldienamines 1 were found to undergo "ionic" Diels-AIder reaction with α,β-unsaturated carbonyl compounds 4 and 6 in the presence of catalytic amounts of p-toluenesulfonic acid. Depending on the structure of the carbonyl compound employed either cyclohexadiene 5 or benzene derivatives 7 are obtained.

Original languageEnglish
Pages (from-to)449-452
Number of pages4
JournalHeterocyclic Communications
Volume3
Issue number5
Publication statusPublished - Dec 1 1997

    Fingerprint

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Kotschy, A., Hajós, G., Timári, G., Messmer, A., & Schantl, J. G. (1997). "Ionic" Diels-Alder reaction of hetaryldienamines. Heterocyclic Communications, 3(5), 449-452.