Application of aminocarbonylation in the synthesis of a lavendamycin synthon

Cedric W. Holzapfel, Wilhelmina Marais

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

An efficient route to a key intermediate in the synthesis of lavendamycin from a suitably substituted 2-chloroquino-line derivative via aminocarbonylation with tryptophan methyl ester as nucleophile, is reported.

Original languageEnglish
Pages (from-to)22-24
Number of pages3
JournalJournal of Chemical Research - Part S
Issue number1
DOIs
Publication statusPublished - 2002

Keywords

  • Aminocarbonylation
  • Lavendamycin
  • Palladium catalysis
  • Quinolines
  • Tryptophan

ASJC Scopus subject areas

  • General Chemistry

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