3-Nitrochromene derivatives as 2π components in 1,3-dipolar cycloadditions of azomethine ylides

A. Virányi, Gabriella Marth, András Dancsó, Gábor Blaskó, L. Tőke, Miklós Nyerges

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

The 1,3-dipolar cycloaddition of 2-aryl-3-nitrochromenes with various azomethine ylides has been investigated. The structure and stereochemistry of cycloadducts were studied in detail by NMR spectroscopic methods.

Original languageEnglish
Pages (from-to)8720-8730
Number of pages11
JournalTetrahedron
Volume62
Issue number37
DOIs
Publication statusPublished - Sep 11 2006

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Stereochemistry
Cycloaddition
Cycloaddition Reaction
Nuclear magnetic resonance
Derivatives
azomethine

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

3-Nitrochromene derivatives as 2π components in 1,3-dipolar cycloadditions of azomethine ylides. / Virányi, A.; Marth, Gabriella; Dancsó, András; Blaskó, Gábor; Tőke, L.; Nyerges, Miklós.

In: Tetrahedron, Vol. 62, No. 37, 11.09.2006, p. 8720-8730.

Research output: Contribution to journalArticle

Virányi, A. ; Marth, Gabriella ; Dancsó, András ; Blaskó, Gábor ; Tőke, L. ; Nyerges, Miklós. / 3-Nitrochromene derivatives as 2π components in 1,3-dipolar cycloadditions of azomethine ylides. In: Tetrahedron. 2006 ; Vol. 62, No. 37. pp. 8720-8730.
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