A novel double 'inverse electron-demand' Diels-Alder reaction of azolyldienamines and tetrazines

András Kotschy, Z. Novák, Zoltán Vincze, David M. Smith, G. Hajós

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Appropriately substituted azolyldienamines were found to undergo double 'inverse electron-demand' Diels-Alder reactions with tetrazine derivatives, yielding azolylpyridazines and dihydropyridazines as products.

Original languageEnglish
Pages (from-to)6313-6316
Number of pages4
JournalTetrahedron Letters
Volume40
Issue number34
DOIs
Publication statusPublished - Aug 20 1999

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Cycloaddition Reaction
Electrons
Derivatives

Keywords

  • Dieis-Alder reactions
  • Dienamines
  • Pyridazines
  • Tetrazines

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

A novel double 'inverse electron-demand' Diels-Alder reaction of azolyldienamines and tetrazines. / Kotschy, András; Novák, Z.; Vincze, Zoltán; Smith, David M.; Hajós, G.

In: Tetrahedron Letters, Vol. 40, No. 34, 20.08.1999, p. 6313-6316.

Research output: Contribution to journalArticle

Kotschy, András ; Novák, Z. ; Vincze, Zoltán ; Smith, David M. ; Hajós, G. / A novel double 'inverse electron-demand' Diels-Alder reaction of azolyldienamines and tetrazines. In: Tetrahedron Letters. 1999 ; Vol. 40, No. 34. pp. 6313-6316.
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