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Dive into the research topics where Jean-Marie Desjobert is active.

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Featured researches published by Jean-Marie Desjobert.


Journal of Chromatography A | 2008

Comparison of liquid-liquid extraction with headspace methods for the characterization of volatile fractions of commercial hydrolats from typically Mediterranean species

Julien Paolini; Christelle Leandri; Jean-Marie Desjobert; Toussaint Barboni; Jean Costa

Chemical composition of volatile fractions of nine commercial hydrolats and corresponding essential oils obtained using an industrial process were studied. The hydrolat volatile fractions were reported for the first time. A comparative study of those obtained, on the one hand, by liquid-liquid extraction (LLE) and, on the other hand, using five solid-phase microextraction (SPME) fibers and also purge-and-trap-automatic thermal desorption (P&T-ATD) was conducted with analysis performed by GC and GC/MS. The use of various techniques has resulted in a change of chromatographic profile of the hydrolat volatile fractions. Quantitative differences were established between chemical compositions of headspace and those obtained by a conventional method (LLE). Statistical analyses were carried out to summarize the results.


Molecular Phylogenetics and Evolution | 2009

Phylogeography of Cistus creticus L. on Corsica and Sardinia inferred by the TRNL-F and RPL32-TRNL sequences of cpDNA

Alessandra Falchi; Julien Paolini; Jean-Marie Desjobert; Alessandra Melis; Jean Costa; Laurent Varesi

2009 Elsevier Inc. All rights reserved.


Industrial Crops and Products | 2002

Composition and chemical variability of the triterpene fraction of dichloromethane extracts of cork (Quercus suber L.)

Vincent Castola; Ange Bighelli; Serge Rezzi; Giovanni Melloni; Serafino Gladiali; Jean-Marie Desjobert; Joseph Casanova

Abstract Dichloromethane extracts were prepared from 38 samples of cork harvested in different locations of Corsica and Sardinia from individual trees of Quercus suber L. Friedelin, 3-α-hydroxyfriedelan-2-one, betulin, betulinic acid, β-sitosterol and sitost-4-en-3-one were identified and their molar percentages were calculated by 13C NMR spectroscopy, following a procedure recently developed by our group. The results were submitted to chemometric analysis (k-means and principal component analysis), which allowed three groups to be distinguished with respect to the content of friedelin, betulinic acid and 3-α-hydroxyfriedelan-2-one.


Phytochemistry | 2011

Chemical and genetic differentiation of Corsican subspecies of Teucrium flavum L.

Nassim Djabou; Marie-José Battesti; Hocine Allali; Jean-Marie Desjobert; Laurent Varesi; Jean Costa; Alain Muselli

Corsica Island exhibited the particularity to display Teucrium flavum subsp. glaucum and subsp. flavum on the same territory with the same bioclimatic conditions. For the first time, volatile components extracted from aerial parts and genetic diversity of both Corsican T. flavum L. subspecies have been investigated through (i) the characterization of the chemical composition of essential oils and (ii) the study of three polymorphic genetic markers. Chemical analysis were performed using combination of capillary GC/RI, GC-MS after fractionation on column chromatography and the definition of the genetic structure were carried out using two chlororoplast markers (RPL32-TRNL and TRNL-F) and ribosomal nuclear markers (ITS region). According to statistical analysis, both subspecies were clearly distinguished by the chemical and genetic studies. Chemical compositions of oils from both subspecies were qualitatively similar but they differed by the normalized% abundances of their major components; oils from subsp. flavum were dominated by large amounts of hydrocarbon monoterpenes while oils obtained from subsp. glaucum were characterized by higher amounts of oxygenated compounds. The genetic analysis divided T. flavum L. populations in two groups, the first displayed subsp. glaucum populations and the latter group exhibited subsp. flavum populations. The presence of two groups is weakly consistent with chemical differentiation. These data suggest that the differences in the volatile composition of the two T. flavum subspecies depends more on the genetic background and less on environmental factors.


Surface Review and Letters | 2009

Application Of Essential Oil Of Artemisia Herba Alba As Green Corrosion Inhibitor For Steel In 0.5 M H2so4

O. Ouachikh; A. Bouyanzer; M. Bouklah; Jean-Marie Desjobert; Jean Costa; B. Hammouti; L. Majidi

Essential oil from Artemisia herba alba (Art) was hydrodistilled and tested as corrosion inhibitor of steel in 0.5 M H2SO4 using weight loss measurements and electrochemical polarization methods. Results gathered show that this natural oil reduced the corrosion rate by the cathodic action. Its inhibition efficiency attains the maximum (74%) at 1 g/L. The inhibition efficiency of Arm oil increases with the rise of temperature. The adsorption isotherm of natural product on the steel has been determined. A. herba alba essential oil was obtained by hydrodistillation and its chemical composition oil was investigated by capillary GC and GC/MS. The major components were chrysanthenone (30.6%) and camphor (24.4%).


Phytochemistry | 2009

Morphological, chemical and genetic differentiation of two subspecies of Cistus creticus L. (C. creticus subsp. eriocephalus and C. creticus subsp. corsicus).

Julien Paolini; Alessandra Falchi; Yann Quilichini; Jean-Marie Desjobert; Marie‐Cecile De Cian; Laurent Varesi; Jean Costa

Cistus creticus L., an aromatic species from the Mediterranean area, contains various diterpenes bearing the labdane skeleton. The production of essential oil from this species has potential economic value, but so far, it has not been optimized. In order to contribute to a better knowledge of this species and to its differentiation, the morphological characters, volatile chemical composition and genetic data of two subspecies (C. creticus subsp. eriocephalus and C. creticus subsp. corsicus) were investigated. The leaf trichomes were studied using scanning electron microscopy. The chemical composition of Corsican essential oil (C. creticus subsp. corsicus) has been reported using GC, GC/MS and 13C NMR; the main constituents were oxygenated labdane diterpenes (33.9%) such as 13-epi-manoyl oxide (18.5%). Using plant material (54 samples) collected from 18 geographically distinct areas of the islands of Corsica and Sardinia, the basis of variation in the headspace solid-phase microextraction volatile fraction and an inter-simple sequence repeat genetic analysis were also examined. It was shown that the two subspecies of C. creticus differed in morphology, essential oil production, volatile fraction composition and genetic data.


Chemistry Central Journal | 2010

Characterization of volatile compounds of Daucus crinitus Desf. Headspace Solid Phase Microextraction as alternative technique to Hydrodistillation

Mohammed El Amine Dib; Nassim Djabou; Jean-Marie Desjobert; Houcine Allali; Boufeldja Tabti; Alain Muselli; Jean Costa

BackgroundTraditionally, the essential oil of aromatic herbs is obtained using hydrodistillation (HD). Because the emitted volatile fraction plays a fundamental role in a plants life, various novel techniques have been developed for its extraction from plants. Among these, headspace solid phase microextraction (HS-SPME) can be used to obtain a rapid fingerprint of a plants headspace. Daucus crinitus Desf. is a wild plant that grows along the west coast of Algeria. Only a single study has dealt with the chemical composition of the aerial part oils of Algerian D. crinitus, in which isochavicol isobutyrate (39.0%), octyl acetate (12.3%), and β-caryophyllene (5.4%) were identified. Using GC-RI and GC-MS analysis, the essential oils and the volatiles extracted from separated organs of D. crinitus Desf. were studied using HS-SPME.ResultsGC-RI and GC-MS analysis identified 72 and 79 components in oils extracted using HD and in the volatile fractions extracted using SPME, respectively. Two types of essential oils were produced by the plant: the root oils had aliphatic compounds as the main component (87.0%-90.1%), and the aerial part oils had phenylpropanoids as the main component (43.1%-88.6%). HS-SPME analysis showed a more precise distribution of compounds in the organs studied: oxygenated aliphatic compounds were well represented in the roots (44.3%-84.0%), hydrocarbon aliphatic compounds were in the leaves and stems (22.2%-87.9%), and phenylpropanoids were in the flowers and umbels (47.9%-64.2%). Moreover, HS-SPME allowed the occurrence of isochavicol (29.6 - 34.7%) as main component in D. crinitus leaves, but it was not detected in the oils, probably because of its solubility in water.ConclusionsThis study demonstrates that HD and HS-SPME modes could be complimentary extraction techniques in order to obtain the complete characterization of plant volatiles.


Food and Chemical Toxicology | 2011

Chemical composition and antioxidant activity of essential oils and solvent extracts of Ptychotis verticillata from Morocco

El Mokhtar El Ouariachi; Pierre Tomi; A. Bouyanzer; B. Hammouti; Jean-Marie Desjobert; Jean Costa; Julien Paolini

The objective of this study was to characterize the chemical composition of the essential oil and extracts of Ptychotis verticillata. The antioxidative activities of this species were also evaluated to suggest it as a new potential source of natural antioxidants. Analysis of the chemical composition of P. verticillata essential oil from Morocco was carried out using GC and GC-MS. The oil was dominated by phenolic compounds (48.0%) with carvacrol (44.6%) and thymol (3.4%) as the main compounds. Plant phenolics constitute one of the major groups of components that act as primary antioxidant free radical terminators. The amounts of total phenolics and flavonoids in the solvent extracts (diethyl ether and ethyl acetate) were determined spectrometrically. Furthermore, the antioxidant activities of the essential oil and extracts were determined using a DPPH test system. The DPPH scavenging activity of extracts increased in the order ethyl acetate>ascorbic acid>diethyl ether>essential oil. Finally, a relationship was observed between the antioxidant activity potential and total phenolic and flavonoid levels of the extract.


Chemical Papers | 2010

Chemical variability of Artemisia herba-alba Asso essential oils from East Morocco

Julien Paolini; El Mokhtar El Ouariachi; A. Bouyanzer; B. Hammouti; Jean-Marie Desjobert; Jean Costa; Alain Muselli

Chemical compositions of 16 Artemisia herba-alba oil samples harvested in eight East Moroccan locations were investigated by GC and GC/MS. Chemical variability of the A. herba-alba oils is also discussed using statistical analysis. Detailed analysis of the essential oils led to the identification of 52 components amounting to 80.5–98.6 % of the total oil. The investigated chemical compositions showed significant qualitative and quantitative differences. According to their major components (camphor, chrysanthenone, and α- and β-thujone), three main groups of essential oils were found. This study also found regional specificity of the major components.


Phytochemical Analysis | 2009

Identification of chrysanthenyl esters from the essential oil of Anthemis maritima L. investigated by GC/RI, GC-MS (EI and CI) and 13C-NMR spectroscopy: chemical composition and variability.

Florent Darriet; Jean-Marie Desjobert; Jean Costa; Alain Muselli

INTRODUCTION Anthemis maritima L. (Asteraceae) is a wild plant growing in Corsica and Sardinia. No previous studies of the chemical composition of A. maritima essential oil have been found. The oil contains two series of cis- and trans-chrysanthenyl esters for which the MS data are not present in available libraries and the 13C-NMR data are not reported in the literature. The determination of these compounds is a challenging problem since some of these esters are present in low concentrations and they exhibit very similar EI-MS. OBJECTIVE To develop comprehensive strategies involving integrated techniques including CC, GC/RI, GC-MS (EI and CI), 1H- and 13C-NMR and hemi-synthesis for the identification of both series of chrysanthenyl esters in A. maritima oils. METHODOLOGY Seventeen oil samples were prepared by hydrodistillation. A fine analysis of a pool of Corsican oils was conducted after repeated CC. A selected Sardinian oil was used as source of product for the hemi-synthesis of chrysanthenyl esters. The identification of these compounds was based on joint information from GC-MS (EI and CI), 13C-NMR and hemi-synthesis. RESULTS Integrated analysis of Corsican and Sardinian oils allowed the identification of 124 components accounting for 83.3-91.6% of the total oil. With the aid of principal component analysis, oil samples could be divided in two groups. Among 16 chrysanthenyl esters identified, 12 were laboratory-synthesised and their 13C-NMR data are reported for the first time. CONCLUSIONS The study illustrates the contribution of integrated techniques for the characterisation of unusual essential oils.

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Jean Costa

Centre national de la recherche scientifique

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Julien Paolini

Centre national de la recherche scientifique

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Alain Muselli

Centre national de la recherche scientifique

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Antoine-François Bernardini

Centre national de la recherche scientifique

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Nassim Djabou

Centre national de la recherche scientifique

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Toussaint Barboni

Centre national de la recherche scientifique

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Marie-José Battesti

Centre national de la recherche scientifique

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Liliane Berti

Centre national de la recherche scientifique

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Nathalie Chiaramonti

Centre national de la recherche scientifique

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