Chemistry of the pseudobasic amino alcohols. Part 40. Synthesis of three new condensed nitrogen heterocyclic systems

Dezsö Korbonits, Benjamin Podányi, Árpád Illár, Kálmán Simon, Miklós Hanusz, I. Hermecz

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Replacement of the central oxygen atom of the heptacyclic condensed diisoquinoline 3 by reaction with hydrazine, hydroxylamine or thiourea in a simple method gave three new heterocyclic ring systems involving 1,2,4,5-tetrazine (7), 1,2,4,5-oxatriazine (8) and 1,2,4,6-tetrazepine (9) central rings.

Original languageEnglish
Pages (from-to)389-395
Number of pages7
JournalHeterocycles
Volume78
Issue number2
DOIs
Publication statusPublished - Feb 1 2009

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hydrazine
Amino Alcohols
Thiourea
Hydroxylamine
Nitrogen
Oxygen
Atoms

Keywords

  • Bis-Pseudosalt
  • Diisoquinoline
  • Heptacycle
  • One-Pot Synthesis

ASJC Scopus subject areas

  • Analytical Chemistry
  • Organic Chemistry
  • Pharmacology

Cite this

Chemistry of the pseudobasic amino alcohols. Part 40. Synthesis of three new condensed nitrogen heterocyclic systems. / Korbonits, Dezsö; Podányi, Benjamin; Illár, Árpád; Simon, Kálmán; Hanusz, Miklós; Hermecz, I.

In: Heterocycles, Vol. 78, No. 2, 01.02.2009, p. 389-395.

Research output: Contribution to journalArticle

Korbonits, Dezsö ; Podányi, Benjamin ; Illár, Árpád ; Simon, Kálmán ; Hanusz, Miklós ; Hermecz, I. / Chemistry of the pseudobasic amino alcohols. Part 40. Synthesis of three new condensed nitrogen heterocyclic systems. In: Heterocycles. 2009 ; Vol. 78, No. 2. pp. 389-395.
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