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Littérature scientifique sur le sujet « Benzoquinones »

Auteur : Grafiati

Publié le 4 juin 2021

Mis à jour le 26 juillet 2025

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Articles de revues sur le sujet "Benzoquinones"

1

Kopecký, Jaroslav, David Šaman, and Ladislav Novotný. "Methylation of substituted 1,4-benzoquinones." Collection of Czechoslovak Chemical Communications 52, no. 1 (1987): 228–32. http://dx.doi.org/10.1135/cccc19870228.

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Methylation of 1,4-benzoquinones I and Ia with diazomethane afforded methyl 15-(6-methoxy-3-methyl-1,4-benzoquinon-2-yl)pentadecanoate (IIa) and methyl 15-(3-methoxy-2,5-dioxobicyclo[4.1.0]hept-3-en-1-yl)pentadecanoate (IIIa), methylation of 1,4-benzoquinone IVa led to methyl 15-(5,6-dimethoxy-3-methyl-1,4-benzoquinon-2-yl)pentadecanoate (Va) and methyl 15-(3,4-dimethoxy-6-methyl-2,5-dioxobicyclo[4.1.0]hept-3-en-1-yl)pentadecanoate (VIa). Structure of the products was established by spectral methods.

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Duarte, Sónia, Ana Magro, Joanna Tomás, Carolina Hilário, Ricardo Boavida Ferreira, and Maria Otília Carvalho. "Antifungal Activity of Benzoquinones Produced by Tribolium castaneum in Maize-Associated Fungi." Insects 13, no. 10 (2022): 868. http://dx.doi.org/10.3390/insects13100868.

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Tribolium castaneum (Herbst) adults produce 1,4-benzoquinone (BQ), methyl-1,4-benzoquinone (MBQ), and ethyl-1,4-benzoquinone (EBQ). These components are chemical defenses used as repellents and irritants, and BQ has a negative impact on the growth of some fungal species. In this work, the inhibitory and/or lethal effects of these benzoquinones on the development of six fungi identified in maize, namely Aspergillus flavus, A. fumigatus, A. niger, Fusarium sp., Penicillium sp., and Trichoderma sp., were evaluated. Ten-day-long disk diffusion trials were performed using benzoquinones. The experim

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Katritzky, Alan R., Herman H. Odens, Michael V. Voronkov, Charles J. Rostek, and Otto W. Maender. "Rubber Chemicals Derived from Conjugate Addition. I. Syntheses of Novel 2-Thio-5-Amino Substituted Benzoquinones." Rubber Chemistry and Technology 74, no. 5 (2001): 915–25. http://dx.doi.org/10.5254/1.3547661.

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Abstract Alkylthio-substituted benzoquinones were prepared from benzoquinone and mercaptans in 50–94% yields via NaIO4 oxidation of the intermediate hydroquinones. Subsequent addition of primary and secondary amines, in the presence of air as an oxidizing agent, gave a range of 2-thio-5-amino-substituted benzoquinones. No oxidation at sulfur was detected under the described conditions.

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Renger, Gernot, Angela Kayed, and Walter Oettmeier. "Interaction of Halogenated 1,4-Benzoquinones with System II of Photosynthesis." Zeitschrift für Naturforschung C 42, no. 6 (1987): 698–703. http://dx.doi.org/10.1515/znc-1987-0609.

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The interaction of halogenated p-benzoquinones with PS II has been analyzed by measurements of fluorescence induction curves and the average oxygen yield per flash in isolated class II chloroplasts. It was found: 1)The normalized area over the fluorescence induction curve in the presence of DCMU. A/Fmax, markedly increases if halogenated p-benzoquinones are added before DCMU. The effect is eliminated by DCMU addition prior to that of the quinones. 2)The extent of A/Fmax increases with increasing dark time between the additions of 2,3.5-tri- bromo-6-methyl-1,4-benzoquinone (TBTO) and DCMU. resp

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KACMAZ, Aysecik. "SYNTHESIS OF MONO(THIO)-, BIS(THIO)- AND MONO(AMINO)-SUBSTITUTED 1,4-BENZOQUINONES." Revue Roumaine de Chimie 69, no. 10-12 (2024): 635–42. https://doi.org/10.33224/rrch.2024.69.10-12.14.

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Twelve thio- and amino- benzoquinones (3a-d, 5a, 5b, 7d, 8d, 10e, 11e, 13e and 13f) were synthesized from benzoquinones (p-benzoquinone 1, p-toluquinone 6 and 2-tert-butyl-1,4-benzoquinone 12) with thiols or primary amines. Among them, compounds 3a-3d and 5a,b have mono(thio)- and bis(thio)- substituted-benzoquinone structures, respectively. The compounds 2-(3,4-dimethylphenylthio)-6- (tetradecylthio)cyclohexa-2,5-diene-1,4-dione (5a) and 2-(3,4- dimethoxyphenylthio)-6-(tetradecylthio)cyclohexa-2,5-diene-1,4-dione, (5b) include two different thio- groups in each of them. Compounds 7d and 8d ha

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Oettmeier, Walter, and Silvana Preuße. "Herbicide and Quinone Binding to Chromatophores and Reaction Centers from Rhodobacter sphaeroides." Zeitschrift für Naturforschung C 42, no. 6 (1987): 690–92. http://dx.doi.org/10.1515/znc-1987-0607.

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Besides s-triazine and triazinone herbicides the chromone stigmatellin and tetrahalogen-substituted 1.4-benzoquinones are inhibitors of photosynthetic electron flow from reduced cytochrome c to ubiquinone-6 in isolated bacterial reaction centers. With isolated bacterial chromatophores binding experiments with radiolabeled herbicides can be performed in a similar way as with thylakoids from higher plants. Tetrahalogen-substituted 1.4-benzoquinones in a Michael type reaction can add onto nucleophilic groups in proteins. In bacterial reaction centers, a [14C]tetra- bromo-1.4-benzoquinone (bromani

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Netzly, David H., James L. Riopel, Gebisa Ejeta, and Larry G. Butler. "Germination Stimulants of Witchweed (Striga asiatica) from Hydrophobic Root Exudate of Sorghum (Sorghum bicolor)." Weed Science 36, no. 4 (1988): 441–46. http://dx.doi.org/10.1017/s0043174500075172.

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Hydrophobic exudate from roots of sorghum [Sorghum bicolor(L.) Moench. #3SORVU ‘IS 8768’] contain fourp-benzoquinones which in the dihydroquinone form are active as germination stimulants of witchweed [Striga asiatica(L.) Kuntz. # STRLU]. The three minorp-benzoquinones were partially characterized and found to be structurally similar to sorgoleone, the majorp-benzoquinone of this exudate. Herbicidal activity of the hydrophobic exudate was due to concentration- and pH-dependent inhibition of root elongation in some but not all weeds tested. Witchweed has apparently adapted these “defense” compo

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Kopecký, Jaroslav, David Šaman, and Ladislav Novotný. "Methoxylation of substituted 1,4-benzoquinones." Collection of Czechoslovak Chemical Communications 52, no. 1 (1987): 223–27. http://dx.doi.org/10.1135/cccc19870223.

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Methoxylation of 1,4-benzoquinones I and Ia with boron trifluoride-methanol complex afforded methyl 15-(5,6-dimethoxy-1,4-benzoquinon-2-yl)pentadecanoate (IIa) and methyl 15-(2-hydroxy-3,5-dimethoxyphenyl)pentadecanoate (IIIa). Structure of the products was established by spectroscopic methods.

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Fernández-Aparicio, Mónica, Marco Masi, Alessio Cimmino, and Antonio Evidente. "Effects of Benzoquinones on Radicles of Orobanche and Phelipanche Species." Plants 10, no. 4 (2021): 746. http://dx.doi.org/10.3390/plants10040746.

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The holoparasitic broomrape weeds (Orobanche and Phelipanche species) cause severe yield losses throughout North Africa, the Middle East, and Southern and Eastern Europe. These parasitic weeds form an haustorium at the tip of their radicles to infect the crop upon detection of the host-derived haustorium-inducing factors. Until now, the haustorial induction in the broomrapes remains less studied than in other parasitic plant species. Known haustorium-inducing factors active in hemiparasites, such as Striga and Triphysaria species, were reported to be inefficient for the induction of haustoria

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Reddy V, Sivarama Krishna, and V. V. Satyanarayana Peruri. "Synthesis of Substituted 1,4-Benzoxazine Derivatives through Diels-Alder Reaction." Caribbean Journal of Science and Technology 07, no. 01 (2019): 88–95. http://dx.doi.org/10.55434/cbi.2019.7111.

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An efficient synthetic protocol is presented for accessing 1,4-benzoxazine derivatives from 2-amino phenol derivatives via o-benzoquinones. The key step involves the Diels-Alder reaction between highly reactive o-quinone monoiminewith butyl vinyl ether/thioether to generate various benzoquinone derivatives.

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Thèses sur le sujet "Benzoquinones"

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Vaysse, Lucile. "Synthese de benzoquinones et de naphtoquinones à activité cutanée potentielle." Université Louis Pasteur (Strasbourg) (1971-2008), 1990. http://www.theses.fr/1990STR13206.

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Ahmad, F. B. H. "Synthesis and reactions of benzoyl-1,4-benzoquinones : an approach to anthracyclinones." Thesis, University of Manchester, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.376238.

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Berger, John Michael. "Isolation, Characterization, and Synthesis of Bioactive Natural Products from Rainforest Flora." Diss., Virginia Tech, 2001. http://hdl.handle.net/10919/28086.

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As part of our ongoing investigations for anticancer drugs from rainforestflora, five plant extracts were determined to contain interesting bioactivity. These extracts were subjected to various separation techniques, affording a number of bioactive compounds that were then characterized by spectral and degradative methods. A methanol extract of Cestrum latifolium Lam. yielded the known compound parissaponin Pb. Hydrolysis afforded its aglycone, the known spirostanol diosgenin. GCMS analysis characterized the derivatized, hydrolyzed sugars. Previous investigations of Albizia subdimidiata pr

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Farard, Julien Duflos Muriel Logé Cédric. "Conception rationnelle, synthèse et évaluation de dérivés hétérocycliques oxygénés à potentialité antitumorale." [S.l.] : [s.n.], 2008. http://castore.univ-nantes.fr/castore/GetOAIRef?idDoc=52276.

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Dassonville, Alexandra. "Synthèse et évaluation pharmacologique de 3,6-diaryl-2,5-dihydroxy-1,4-benzoquinones à activité insulinomimétique." Nantes, 2003. http://archive.bu.univ-nantes.fr/pollux/show.action?id=90b76ad2-9f9a-4712-8e65-3490fc45bb5d.

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La déméthylasterriquinone B1 est une molécule naturelle, non peptidique, récemment découverte, après screening, pour ses propriétés insulinomimétiques. C'est dans ce cadre que nous avons développé une stratégie de synthèse pour la préparation de 3,6-diaryl-2,5-dihydroxy-1,4-benzoquinones, analogues de ce composé. Ainsi, l'accès à ces benzoquinones peut-être envisagé à partir de 3-aryl-1-hydroxypropan-2-ones via des 4-aryl-6-arylméthylidène-3-hydroxypyrane-2,5-diones, produits provenant de la condensation de 4-aryl-3-hydroxypyrane-2,5-diones et de dérivés aromatiques formylés. Aussi, de nombreu

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Dassonville, Alexandra Le Baut Guillaume. "Synthèse et évaluation pharmacologique de 3,6-diaryl-2,5-dihydroxy-1,4-benzoquinones à activité insulinomimétique." [S.l.] : [s.n.], 2003. http://theses.univ-nantes.fr/thesemed/DOCdassonville.pdf.

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SUFI, BIANCA da S. "Utilização de cocultura de melanócitos e queratinócitos para avaliação da ação do líquido da castanha de caju (LCC) na pigmentação epidérmica." reponame:Repositório Institucional do IPEN, 2013. http://repositorio.ipen.br:8080/xmlui/handle/123456789/10197.

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Made available in DSpace on 2014-10-09T12:35:54Z (GMT). No. of bitstreams: 0<br>Made available in DSpace on 2014-10-09T14:03:26Z (GMT). No. of bitstreams: 0<br>Dissertação (Mestrado)<br>IPEN/D<br>Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

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Farard, Julien. "Conception rationnelle, synthèse et évaluation de dérivés hétérocycliques oxygénés à potentialité antitumorale." Nantes, 2008. https://archive.bu.univ-nantes.fr/pollux/show/show?id=f40d012d-692b-402b-99de-c93d12be5595.

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Malgré la découverte de nouvelles molécules antitumorales et l'application de nouveaux traitements, le cancer reste une des principales causes de décès dans les pays développés. Des travaux antérieurs réalisés au laboratoire ont montré que des composés à structure 1,4-benzoquinone possédaient des activités sur la protéine anti-apoptotique Bcl-XL et sur la protéine tyrosine kinase Src, toutes deux impliquées dans des pathologies cancéreuses. Dans le prolongement de ces travaux, des pharmacomodulations ont été réalisées autour du noyau benzoquinone, sans permettre l'amélioration des activités ex

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Béarnais-barbry, Stéphane. "Etude de photoréactivité de la méthoxy-p-quinone et de phényl-p-benzoquinones en solution." Bordeaux 1, 2001. http://www.theses.fr/2001BOR12394.

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L'étude de la photoréactivité du couple méthoxy-p-quinone/méthoxyhydroquinone en solution a permis d'appréhender son importance dans la photodégradation des pâtes à papier à haut rendement. Le mécanisme de la photocyclisation de diverses phényl-p-benzoquinones et d'un analogue, la 4,4'-diméthoxyhydroquinone, a été déterminé par irradiation continue et spectroscopie résolue dans le temps.

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Gan, Daqing. "Aqueous photochemistry of 1,4-benzoquinones and their possible role in the photochemistry of natural organic matter." College Park, Md. : University of Maryland, 2005. http://hdl.handle.net/1903/2180.

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Thesis (Ph. D.)--University of Maryland, College Park, 2005.<br>Thesis research directed by: Chemistry. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.

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Livres sur le sujet "Benzoquinones"

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Lusthof, Klaas Jurjen. Potential antitumor bis(aziridinyl)benzoquinones and DNA: Alkylation and redox cycling = Potentiële bis(aziridinyl) benzochinoncytostatica en DNA : alkylering en redox cycling. [s.n.], 1990.

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Spectroscopic Investigation of Charge Transfer Complexes of 4-Aminoacetanilide with Series of Substituted 1, 4-Benzoquinones. ASDF International, 2017.

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Sainsbury, Malcolm. Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds : Aromatic Compounds : Part B: Benzoquinones and Related Compounds: Derivatives ... Aralkyl Compounds, (Aromatic Compounds). Elsevier Publishing Company, 1995.

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Edited by: H. J. Arpe. Antidiabetic Drugs to Benzoquinone and Naphthoquinone Dyes, Volume A3, Ullmann's Encyclopedia of Industrial Chemistry. 5th ed. Wiley-VCH, 1985.

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Ullman's Encyclopedia of Industrial Chemistry. Vol A3 Antidiabetic drugs to benzoquinone and naphthoquinone dyes. 5th ed. VCH, 1985.

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Barjesteh, Hengameh. Studies of complexes derived from 5-acetylamino-1,2- benzoquinone 2-oxime and related ligands. 1991.

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Ekcan, Ismail. Metal complexes of selected 5-Alkylamino-1,2-benzoquinone-2-oximes and their applicability in solvent extraction. 2001.

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Numan, Abdulqawi Ahmad. Spectrophotometric determination of diaminopyrimidines with p-benzoquinone and on-line photochemical derivatization of sulfa drugs and indoles using liquid chromatography/mass spectrometry. 2001.

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Yamamotot, Y. Stephen. Ullmann's Encyclopedia of Industrial Chemistry: Antidiabetic Drugs to Benzoquinone and Napthoquinone, Vol A3 (Ullmann's Encyclopedia of Industrial Chemistry 5th ed Vol a). 5th ed. Vch Pub, 1985.

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Baker, Lillian Eloise. The Effect Of Substitution On The Free Energy Of Reduction Of Benzoquinone; Including A Study Of The Electrometric Titration Method Of Measuring Potentials. Kessinger Publishing, LLC, 2007.

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Chapitres de livres sur le sujet "Benzoquinones"

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Thomson, R. H. "Benzoquinones." In Naturally Occurring Quinones IV. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-1551-0_1.

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Seigler, David S. "Benzoquinones, Naphthoquinones, and Anthraquinones." In Plant Secondary Metabolism. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4913-0_6.

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Folle, G. A., and S. López de Griego. "Clastogenicity of Methylated p-Benzoquinones: Chemical Warfare in Nature?" In Cytogenetics. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72802-0_18.

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Nitschke, W., D. M. Kramer, A. Riedel, and U. Liebl. "From Naphtho- to Benzoquinones - (R)evolutionary Reorganisations of Electron Transfer Chains." In Photosynthesis: from Light to Biosphere. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-009-0173-5_225.

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Gooch, Jan W. "p-Benzoquinone." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1226.

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Satoh, Kazuhiko, Yuki Kitatani, Toshiaki Ichimura, and Sakae Katoh. "Interactions Between Various Benzoquinones and the QB Site of Oxygen-Evolving Photosystem II Preparations from the Thermophilic Cyanobacterium Synechococcus elongatus." In Current Research in Photosynthesis. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_134.

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Calbo, Joaquín, Juan Aragó, and Enrique Ortí. "Theoretical study of the benzoquinone–tetrathiafulvalene–benzoquinone triad in neutral and oxidized/reduced states." In Highlights in Theoretical Chemistry. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-41272-1_18.

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Jowa, L., S. Winkle, G. Kalf, G. Witz, and R. Snyder. "Deoxyguanosine Adducts Formed from Benzoquinone and Hydroquinone." In Biological Reactive Intermediates III. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5134-4_78.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron complex with Schiff base and o-benzoquinone ligands." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_321.

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Li, Fangbiao, Kenneth Shelly, Carolyn B. Knobler, and M. Frederick Hawthorne. "Benzoquinone Oxidation of the [ae-B20H17NH3]3- and [ae-B20H17OH]4- Ions." In Frontiers in Neutron Capture Therapy. Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1285-1_118.

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Actes de conférences sur le sujet "Benzoquinones"

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Zhang, Jiezheng, Cheng Fan, and Kening Sun. "Imine-based covalent organic framework containing benzoquinone active units as a cathode material for lithium-ion batteries." In Tenth International Conference on Energy Materials and Electrical Engineering (ICEMEE 2024), edited by Yuanhao Wang and Cristian Paul Chioncel. SPIE, 2024. https://doi.org/10.1117/12.3050804.

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Iniesta, Jesus, Mariam al Azani, Mazen al Sulaibi, Thies Thiemann, Miguel Ángel Montiel, and Carlos Sánchez sánchez. "Synthesis and electrochemical redox properties of arylated p-benzoquinones, naphthoquinones and alkylamidoalkyl-p-benzoquinones." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a014.

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Thiemann, Thies, Mariam Al Azani, Nuha al Soom, Jesus Iniesta, and Thies Thiemann. "Facile access to amidoethyl-p-benzoquinones." In The 19th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a035.

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Thiemann, Thies, Nuha al Soom, and Saber Elsuccary. "Preparation of methoxy-substituted para-benzoquinones." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a007.

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Donatoni, Maria Carolina, Timothy John Brocksom, Marciana P. Uliana, and Kleber T. de Oliveira. "The Diels-Alder reactions of carbomethoxy-p-benzoquinones with simple dienes." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0197-1.

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Johnston, Martin, Melissa Latter, Ronald Warrener, Mirta Golic, Dan McKavanagh, and Davor Margetic. "Diels-Alder cycloadditions of 1,3-cyclohexadien-4,5-diones(o-benzoquinones) with norbornadiene. Part I. Synthesis." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01837.

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Servilha, Bruno M., Maria C. Donatoni, Kleber T. de Oliveira, Marco A. B. Ferreira, and Timothy J. Brocksom. "An experimental and theoretical study of the cycloaddition reactions of carbomethoxy-para-benzoquinones with 6,6-dimethyl-fulvene." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20139416531.

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Donatoni, Maria C., Gilmar A. B. Junior, Alcindo A. Dos Santos, Kleber T. de Oliveira, and Timothy J. Brocksom. "The Diels-Alder reaction of para-benzoquinones and simple dienes under catalysis with FeCl3 on Aerosil® silica." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013913152849.

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Saputra, Rizki Rachmad, Siti Mariyah Ulfa, and M. Farid Rahman. "Novel bromoalkyl-1,4-benzoquinones as anti-inflammatory candidate toward COX signaling: Synthesis, octanol-water solubility, and in-silico drug-target profiling." In INTERNATIONAL CONFERENCE ON ORGANIC AND APPLIED CHEMISTRY (ICOAC) 2022. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0193623.

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Chang, Chuan-Hsin, Russell Kitson, Philip Reigan, David Siegel, Christopher J. Moody, and David Ross. "Abstract B102: 19-Substituted benzoquinone ansamycins: Decreasing the toxicity of the benzoquinone ansamycin class of Hsp90 inhibitors." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-b102.

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Rapports d'organisations sur le sujet "Benzoquinones"

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Mbiya, Wilbes. Substituent Effects on Reactivity and Allergenicity of Benzoquinone. Portland State University Library, 2000. http://dx.doi.org/10.15760/etd.1406.

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2

Savova, Gergana, Katya Stankova, Nevena Aneva, and Rayna Boteva. Geldanamycin, Natural Benzoquinone and Inhibitor of the Molecular Chaperone Hsp90, Accelerates the Repair of DNA Doublestrand Breaks in Human Blood Cells. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2021. http://dx.doi.org/10.7546/crabs.2021.05.08.

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