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

M. Nyerges, I. Fejes, L. Tőke

Research output: Contribution to journalArticle

55 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. (C) 2000 Elsevier Science Ltd.

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

Fingerprint

Cycloaddition
Cycloaddition Reaction
martinelline
martinellic acid
azomethine

Keywords

  • Amino acids and derivatives
  • Cycloadditions
  • Pyrrolidines
  • Quinolines

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

An intermolecular 1,3-dipolar cycloaddition approach to the tricyclic core of martinelline and martinellic acid. / Nyerges, M.; Fejes, I.; Tőke, L.

In: Tetrahedron Letters, Vol. 41, No. 41, 07.10.2000, p. 7951-7954.

Research output: Contribution to journalArticle

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