Ring opening of [1,2,3]triazolo[1,5-a]pyrazinium salts: Synthesis and some transformations of a novel type of 2-aza-1,3-butadienes

Mariann Béres, G. Hajós, Z. Riedl, Géza Timári, András Messmer, S. Holly, Joachim G. Schantl

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

The synthesis of 1,3-disubstituted [1.2.3]triazolo[1,5-a]pyrazinium salts 6 and subsequent ring opening induced by the reaction with pyrrolidine provides a facile access to 4-(1-pyrrolidino)-1-([1,2,3] triazol-5-yl)-2-aza-1,3-butadienes 7, a new type of 2-aza-1,3-butadienes. Compounds 7 proved to be suitable starting materials for further ring formation reactions.

Original languageEnglish
Pages (from-to)9393-9400
Number of pages8
JournalTetrahedron
Volume53
Issue number27
DOIs
Publication statusPublished - Jul 7 1997

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Salts
1,3-butadiene
pyrrolidine

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Ring opening of [1,2,3]triazolo[1,5-a]pyrazinium salts : Synthesis and some transformations of a novel type of 2-aza-1,3-butadienes. / Béres, Mariann; Hajós, G.; Riedl, Z.; Timári, Géza; Messmer, András; Holly, S.; Schantl, Joachim G.

In: Tetrahedron, Vol. 53, No. 27, 07.07.1997, p. 9393-9400.

Research output: Contribution to journalArticle

Béres, Mariann ; Hajós, G. ; Riedl, Z. ; Timári, Géza ; Messmer, András ; Holly, S. ; Schantl, Joachim G. / Ring opening of [1,2,3]triazolo[1,5-a]pyrazinium salts : Synthesis and some transformations of a novel type of 2-aza-1,3-butadienes. In: Tetrahedron. 1997 ; Vol. 53, No. 27. pp. 9393-9400.
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