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Chemical Diversity of Essential Oils from Asteriscus graveolens (Forssk.) Less.: Identification of cis‐8‐Acetoxychrysanthenyl Acetate as a New Natural Component
Authors:Gregory Cristofari  Mohamed Znini  Lhou Majidi  Hamid Mazouz  Pierre Tomi  Jean Costa  Julien Paolini
Institution:1. Université de Corse, CNRS UMR 6134, Laboratoire de Chimie des Produits Naturels, FR‐BP 52 Corte, (phone: +33‐4?95?45?01?93;2. fax: +33‐4?95?45?01?62);3. Laboratoire des Substances Naturelles & Synthèse et Dynamique Moléculaire, Faculté des Sciences et Techniques, Errachidia, Morocco;4. Laboratoire de Protection & Amélioration et Ecophysiologie Végétale, Faculté des Sciences et Techniques, Errachidia, Morocco
Abstract:Asteriscus graveolens is an endemic medicinal plant mainly distributed in south‐western Algeria and south‐eastern Morocco. The essential oils of leaves, stems, and flowers of A. graveolens had been studied by GC, GC/MS, and 13C‐NMR. The spectral data of two nerolidol derivatives, 6‐oxo‐ and 6‐hydroxycyclonerolidol, were reassigned by 1D‐ and 2D‐NMR spectroscopy. These compounds can be considered as chemical markers of this genus. The structure of a monoterpenic diester with a chrysanthenane skeleton, i.e., cis‐8‐acetoxychrysanthenyl acetate, was determined for the first time on the basis of GC/MS, and 1D‐ and 2D‐NMR. The stem and leaf oils were characterized by high content of oxygenated sesquiterpenes with 6‐oxo‐ and 6‐hydroxycyclonerolidol as major components, and the flower essential oils were dominated by the new monoterpenic compound cis‐8‐acetoxychrysanthenyl acetate.
Keywords:Asteriscus graveolens  Cyclonerolidol  Chrysanthenyl acetate  cis‐8‐acetoxy‐  Essential oils
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