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


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
Issue number10
Publication statusPublished - Oct 2007



  • 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.