An intermolecular 1,3-dipolar cycloaddition approach to the tricyclic core of martinelline and martinellic acid

M. Nyerges, I. Fejes, L. Toke

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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. (C) 2000 Elsevier Science Ltd.

Original languageEnglish
Pages (from-to)7951-7954
Number of pages4
JournalTetrahedron Letters
Volume41
Issue number41
DOIs
Publication statusPublished - Oct 7 2000

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Keywords

  • Amino acids and derivatives
  • Cycloadditions
  • Pyrrolidines
  • Quinolines

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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