2017
DOI: 10.19261/cjm.2017.410
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Thionation of Essential Oils from Algerian Artemisia Herba-alba L. and Ruta Montana L.: Impact on their Antimicrobial and Insecticidal Activities

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Cited by 10 publications
(16 citation statements)
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“…Other known compounds were first tentatively identified through MS library matching technique (Table 1) and then after the isolation of constituents the structures were confirmed by comparison of the spectral data ( 1 HNMR, 13 CNMR and MS) with that reported in literature. Thus compound 1 was identified as artemisinin, [25] compound 2 as deoxy artemisinin25, compound 3 as gorgonolide, [6] compound 4 as 1‐β, 10‐α‐dihydroxy‐1,10 deoxygorgonolide, [6] compound 5 a as yangambin and 5 b as epi‐yangambin, [26] compound 6 as casticin also named as vitexicarpin, [27] compound 7 as 7,22‐ergostanediene‐3‐ol, [23] compound 8 as undecanol, [28] compound 9 as artabsinolide diepoxide, [29] compound 11 as campsterol, [30] compound 12 as stigmasterol, [30] compound 13 as artabsinolide A and compound 14 as artabsinolide C [29] . All the constituents were isolated using repeated normal phase column chromatography with varying polarity of mobile phase.…”
Section: Resultsmentioning
confidence: 99%
“…Other known compounds were first tentatively identified through MS library matching technique (Table 1) and then after the isolation of constituents the structures were confirmed by comparison of the spectral data ( 1 HNMR, 13 CNMR and MS) with that reported in literature. Thus compound 1 was identified as artemisinin, [25] compound 2 as deoxy artemisinin25, compound 3 as gorgonolide, [6] compound 4 as 1‐β, 10‐α‐dihydroxy‐1,10 deoxygorgonolide, [6] compound 5 a as yangambin and 5 b as epi‐yangambin, [26] compound 6 as casticin also named as vitexicarpin, [27] compound 7 as 7,22‐ergostanediene‐3‐ol, [23] compound 8 as undecanol, [28] compound 9 as artabsinolide diepoxide, [29] compound 11 as campsterol, [30] compound 12 as stigmasterol, [30] compound 13 as artabsinolide A and compound 14 as artabsinolide C [29] . All the constituents were isolated using repeated normal phase column chromatography with varying polarity of mobile phase.…”
Section: Resultsmentioning
confidence: 99%
“…Pneumonie , Pseudomonas fluorescence , Pseudomonas putida , Shigella sp., Staphylococcus epidermidis , Streptococcus agalactiae , and Streptococcus groupe. In another study, the essential oil of the aerial parts was found to be inactive against Escherichia coli but showed significant activity against Staphylococcus aureus with a zone of inhibition of 18 mm [ 70 ].…”
Section: Bioactivitiesmentioning
confidence: 99%
“…The major antifungal activity of the essential oil of the aerial part of R. montana was against Aspergillus , Alternaria , and Candida species [ 18 , 67 , 70 , 71 , 72 , 73 , 84 ]. This essential oil was also found to be active against Saccharomyces cerevisiae (12–15 mm) [ 67 ]), Cryptococcus neoformans (20 mm), Fusarium sp.…”
Section: Bioactivitiesmentioning
confidence: 99%
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“…Previous studies have shown that R. montana can be considered as an important source of biologically interesting compounds, namely alkaloids, coumarins, flavonoids, tannins and essential oils (Kambouche et al, 2008;Boutoumi et al, 2009;Belkessame et al, 2011;Bouzidi et al, 2012; Synergistic effects of Ruta montana (Clus.) L. essential oil and antibiotics against some pathogenic bacteria et al, 2012; Hammiche et al, 2013;Ferhat et al, 2014;Khadhri et al, 2014;Hammami et al, 2015;Hazzit et al, 2015;Daoudi et al, 2016;Bennaoum et al, 2017;Fekhar et al, 2017;Benali et al, 2020;Drioiche et al, 2020;Mohammedi et al, 2020), with biological activities including antioxidant (Kambouche et al, 2008;Zellagui et al,2012;Benali et al, 2020;Mohammedi et al, 2020), antifungal (Hammami et al, 2015;Hazzit et al, 2015;Fekhar et al, 2017;Benali et al, 2020;Drioiche et al, 2020;Mohammedi et al, 2020), insecticidal and larvicidal (Boutoumi et al, 2009;Fekhar et al, 2017).…”
Section: Introductionmentioning
confidence: 99%