Relative stereochemistry of a diterpene from Salvia cinnabarina

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.

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Bibliographic Details
Published inMolecules (Basel, Switzerland) Vol. 12; no. 10; pp. 2279 - 2287
Main Authors Bisio, Angela, Pagano, Bruno, Romussi, Alessia, Bruno, Olga, De Tommasi, Nunziatina, Romussi, Giovanni, Mattia, Carlo Andrea
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 10.10.2007
MDPI
Subjects
Crystallography, X-Ray
Diterpenes - chemistry
Hydrogen bonds
Lamiaceae
Magnetic Resonance Spectroscopy
Models, Molecular
Molecular Structure
Plant Extracts - chemistry
Plants, Medicinal - chemistry
relative stereo- Salvia cinnabarina
relative stereo-chemistry
Salvia - chemistry
Salvia cinnabarina
secoisopimarane-diterpene
Single crystals
Stereoisomerism
X-ray structure
Italy
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Summary: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.
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ISSN:1420-3049
1420-3049
DOI:10.3390/12102279