Synthesis of new quinoline derivatives

J. Tóth, Gábor Blaskó, András Dancsó, L. Tőke, Miklós Nyerges

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

The synthesis of some new functionalized quinolyl derivatives has been described, based on the 1,3-dipolar cycloaddition of an azomethine ylide, generated from sarcosine or N-benzylglycine and paraformaldehyde, to 2-chloro-3-quinolinecarbaldehydes.

Original languageEnglish
Pages (from-to)3581-3589
Number of pages9
JournalSynthetic Communications
Volume36
Issue number23
DOIs
Publication statusPublished - Nov 1 2006

Fingerprint

Sarcosine
Cycloaddition
Derivatives
paraform
azomethine
N-benzylglycine
quinoline

Keywords

  • Dipolar cycloaddition
  • Multicomponent reactions
  • Oxazolines
  • Quinolines

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Synthesis of new quinoline derivatives. / Tóth, J.; Blaskó, Gábor; Dancsó, András; Tőke, L.; Nyerges, Miklós.

In: Synthetic Communications, Vol. 36, No. 23, 01.11.2006, p. 3581-3589.

Research output: Contribution to journalArticle

Tóth, J, Blaskó, G, Dancsó, A, Tőke, L & Nyerges, M 2006, 'Synthesis of new quinoline derivatives', Synthetic Communications, vol. 36, no. 23, pp. 3581-3589. https://doi.org/10.1080/00397910600943568
Tóth, J. ; Blaskó, Gábor ; Dancsó, András ; Tőke, L. ; Nyerges, Miklós. / Synthesis of new quinoline derivatives. In: Synthetic Communications. 2006 ; Vol. 36, No. 23. pp. 3581-3589.
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