A convenient synthesis of the pyrrolo[3,2-c]quinoline core of martinelline alkaloids

Miklós Nyerges, Imre Fejes, L. Tőke

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

The tricyclic core of the martinellines has been synthesised stereoselectively in two steps, using 1,3-dipolar cycloaddition of azomethine ylides as a key step.

Original languageEnglish
Pages (from-to)1823-1828
Number of pages6
JournalSynthesis
Issue number13
Publication statusPublished - 2002

Fingerprint

Alkaloids
Cycloaddition
quinoline
azomethine
martinelline

Keywords

  • Amino acids and derivatives
  • Cycloadditions
  • Pyrrolidines
  • Quinolines

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

A convenient synthesis of the pyrrolo[3,2-c]quinoline core of martinelline alkaloids. / Nyerges, Miklós; Fejes, Imre; Tőke, L.

In: Synthesis, No. 13, 2002, p. 1823-1828.

Research output: Contribution to journalArticle

Nyerges, Miklós ; Fejes, Imre ; Tőke, L. / A convenient synthesis of the pyrrolo[3,2-c]quinoline core of martinelline alkaloids. In: Synthesis. 2002 ; No. 13. pp. 1823-1828.
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