Relative stereochemistry of a diterpene from Salvia cinnabarina

Angela Bisio, Bruno Pagano, Alessia Romussi, Olga Bruno, Nunziatina De Tommasi, Giovanni Romussi, Carlo Andrea Mattia

Research output: Contribution to journalArticle

Abstract

The relative stereochemistry of 3,4-secoisopimara-4(18),7,15-triene-3-oic acid, a diterpenoid with antispasmodic, hypotensive and antibacterial activities isolated from Salvia cinnabarina, was determined by an X-ray diffraction analysis of a single crystal of a suitable crystalline derivative.

Original languageEnglish
Pages (from-to)2279-2287
Number of pages9
JournalMolecules
Volume12
Issue number10
DOIs
Publication statusPublished - Oct 2007

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Keywords

  • Lamiaceae
  • Relative stereochemistry
  • Salvia cinnabarina
  • Secoisopimarane-diterpene
  • X-ray structure

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Bisio, A., Pagano, B., Romussi, A., Bruno, O., De Tommasi, N., Romussi, G., & Mattia, C. A. (2007). Relative stereochemistry of a diterpene from Salvia cinnabarina. Molecules, 12(10), 2279-2287. https://doi.org/10.3390/12102279