Synthetic Studies on Pandanus Alkaloids: From Norpandamarilactonines to Pandamarilactonines, a Proof of Their Configurational Instability

Pilar Blanco, Felix Busqué, Pedro De March, Marta Figueredo, Josep Font, Elena Sanfeliu

Research output: Contribution to journalArticleResearchpeer-review

13 Citations (Scopus)

Abstract

The ethyl carbamate of norpandamarilactonine-A was prepared in an enantiomerically pure form starting from (S)-prolinol, Deprotection of the amine functionality rendered both diastereomeric norpandamarilactonines as racemates, which were used as synthetic precursors of pandamarilactonine-A and -B. © Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
Original languageEnglish
Pages (from-to)48-53
JournalEuropean Journal of Organic Chemistry
Issue number1
DOIs
Publication statusPublished - 1 Jan 2004

Keywords

  • Alkaloids
  • Configurational stability
  • Total synthesis

Fingerprint

Dive into the research topics of 'Synthetic Studies on Pandanus Alkaloids: From Norpandamarilactonines to Pandamarilactonines, a Proof of Their Configurational Instability'. Together they form a unique fingerprint.

Cite this