Relevant bibliographies by topics / Furanones

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  2. Dissertations / Theses
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Academic literature on the topic 'Furanones'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 July 2025

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Journal articles on the topic "Furanones"

1

Ndagijimana, Maurice, Melania Vallicelli, P. Sandro Cocconcelli, et al. "Two 2[5H]-Furanones as Possible Signaling Molecules in Lactobacillus helveticus." Applied and Environmental Microbiology 72, no. 9 (2006): 6053–61. http://dx.doi.org/10.1128/aem.00363-06.

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ABSTRACT Two 2[5H]-furanones, in association with medium-chain fatty acids, were released in whey by Lactobacillus helveticus exposed to oxidative and heat stresses. This species plays an important role in cheese technology, particularly for Swiss-type cheeses and Grana cheese. Moreover, it significantly contributes to cheese ripening by means of an early autolysis and the release of enzymes during processing. Experimental evidence of the involvement of the two 2[5H]-furanones, detected by a gas chromatography-mass spectrometry/solid-phase microextraction technique, in the autolysis phenomenon
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Janssens, Joost C. A., Hans Steenackers, Stijn Robijns, et al. "Brominated Furanones Inhibit Biofilm Formation by Salmonella enterica Serovar Typhimurium." Applied and Environmental Microbiology 74, no. 21 (2008): 6639–48. http://dx.doi.org/10.1128/aem.01262-08.

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ABSTRACT Salmonella enterica serovar Typhimurium is a main cause of bacterial food-borne diseases. As Salmonella can form biofilms in which it is better protected against antimicrobial agents on a wide diversity of surfaces, it is of interest to explore ways to inhibit biofilm formation. Brominated furanones, originally extracted from the marine alga Delisea pulchra, are known to interfere with biofilm formation in several pathogens. In this study, we have synthesized a small focused library of brominated furanones and tested their activity against S. enterica serovar Typhimurium biofilm forma
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Rodríguez-López, Pedro, Andrea Emparanza Barrenengoa, Sergio Pascual-Sáez, and Marta López Cabo. "Efficacy of Synthetic Furanones on Listeria monocytogenes Biofilm Formation." Foods 8, no. 12 (2019): 647. http://dx.doi.org/10.3390/foods8120647.

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Furanones are analogues of acylated homoserine lactones with proven antifouling activity in both Gram-positive and Gram-negative bacteria though the interference of various quorum sensing pathways. In an attempt to find new strategies to prevent and control Listeria monocytogenes biofilm formation on stainless steel (SS) surfaces, different concentrations of six synthetic furanones were applied on biofilms formed by strains isolated from food, environmental, and clinical sources grown onto AISI 316 SS coupons. Among the furanones tested, (Z-)-4-Bromo-5-(bromomethylene)-2(5H)-furanone and 3,4-D
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Huang, Huicai, Xue Lu, Yukang Mao, and Jinxing Ye. "Asymmetric synthesis of highly functionalized furanones via direct Michael reactions mediated by a bulky primary amine." Organic Chemistry Frontiers 6, no. 8 (2019): 1080–83. http://dx.doi.org/10.1039/c8qo01132j.

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Żurawska, Katarzyna, Anna Byczek-Wyrostek, Anna Kasprzycka, and Krzysztof Walczak. "3,4-Dihalo-5-hydroxy-2(5H)-furanones: Highly Reactive Small Molecules." Molecules 29, no. 21 (2024): 5149. http://dx.doi.org/10.3390/molecules29215149.

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3,4-Dichloro-5-hydroxy-2(5H)-furanone and its dibromo analog are highly reactive molecules. Both are members of the 2(5H)-furanone family, which are important as pharmacophores present in drugs and natural products. Compounds possessing the 2(5H)-furanone skeleton isolated from plants and marine organisms exhibit bioactivity against various microorganisms and viruses and can also be used in other medical treatments. The structures of these 3,4-dihalo-2(5H)-furanones cause their high reactivity due to the presence of a carbonyl group on the C2 carbon conjugated with a double bond and a hydroxyl
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Liao, Liang, and Didier Villemin. "A Rapid and Efficient One-Pot Synthesis of Substituted 2-(5H)-furanones under focused microwave irradiations." Journal of Chemical Research 2000, no. 4 (2000): 179–81. http://dx.doi.org/10.3184/030823400103166869.

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3-Hydroxy-3-methyl-2-butanone 1 reacted with ethyl cyanocetate in 2 in the presence of sodium ethoxide under focused microwave irradiations to afford 3-cyano-4,5,5-trimethyl-2-( 5H)-furanone 3. Furanone 3 then condensed with aromatic or heteroaromatic aldehydes 4a–h to produce 3-cyano-4-( trans-aryl-vinyl)-5,5-dimethyl-2-( 5H)-furanones 5a–h in high overall yields (71–88%).
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Viturro, Carmen I., Juana R. de la Fuente, and Marta S. Maier. "One New Prenylated Furanone and Other non Polar Constituents from Mutisia friesiana." Zeitschrift für Naturforschung B 60, no. 5 (2005): 585–89. http://dx.doi.org/10.1515/znb-2005-0519.

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In addition to the known furanones 1 and 2, the aerial parts of the shrub Mutisia friesiana afforded a new prenylated furanone, Mutisifuranone A (3), together with the known triterpenoids oleanic (4) and ursolic (5) acids and some sesquiterpenoids and n-alkanes. Their structures were elucidated by spectroscopic methods.
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Muñoz-Cázares, Naybi, Israel Castillo-Juárez, Rodolfo García-Contreras, et al. "A Brominated Furanone Inhibits Pseudomonas aeruginosa Quorum Sensing and Type III Secretion, Attenuating Its Virulence in a Murine Cutaneous Abscess Model." Biomedicines 10, no. 8 (2022): 1847. http://dx.doi.org/10.3390/biomedicines10081847.

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Quorum sensing (QS) and type III secretion systems (T3SSs) are among the most attractive anti-virulence targets for combating multidrug-resistant pathogenic bacteria. Some halogenated furanones reduce QS-associated virulence, but their role in T3SS inhibition remains unclear. This study aimed to assess the inhibition of these two systems on Pseudomonas aeruginosa virulence. The halogenated furanones (Z)-4-bromo-5-(bromomethylene)-2(5H) (C-30) and 5-(dibromomethylene)-2(5H) (named hereafter GBr) were synthesized, and their ability to inhibit the secretion of type III exoenzymes and QS-controlle
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Markus, Victor, Karina Golberg, Kerem Teralı, et al. "Assessing the Molecular Targets and Mode of Action of Furanone C-30 on Pseudomonas aeruginosa Quorum Sensing." Molecules 26, no. 6 (2021): 1620. http://dx.doi.org/10.3390/molecules26061620.

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Quorum sensing (QS), a sophisticated system of bacterial communication that depends on population density, is employed by many pathogenic bacteria to regulate virulence. In view of the current reality of antibiotic resistance, it is expected that interfering with QS can address bacterial pathogenicity without stimulating the incidence of resistance. Thus, harnessing QS inhibitors has been considered a promising approach to overriding bacterial infections and combating antibiotic resistance that has become a major threat to public healthcare around the globe. Pseudomonas aeruginosa is one of th
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Hosseinzadeh, Zahra, and Ali Ramazani. "An Overview of the Chemistry and Pharmacological Potentials of Furanones Skeletons." Current Organic Chemistry 23, no. 14 (2019): 1581–99. http://dx.doi.org/10.2174/1385272823666190820111928.

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The furanone structure, a significant group of heterocyclic compounds, is frequently found in natural products that are exhibiting striking pharmacological effects and a growing field of research. They have a wide spectrum of pharmaceutical activity: anticataract, anticancer, antibacterial, anti-inflammatory, anticonvulsant. This review article presents a summary of natural furanones, synthetic methods, and the biological effects of these important compounds. Solid-phase method, cross-coupling reactions, Maillard-type reaction, the cycloaddition of alcohol and phenyl nitrile oxide, and side-ch
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Dissertations / Theses on the topic "Furanones"

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Bennett, Mandy. "Synthesis of 2(5H)-furanones." Thesis, University of Nottingham, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.334768.

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Hayashida, Yasuo. "The furanones in Japanese barley miso flavour." Thesis, Heriot-Watt University, 2000. http://hdl.handle.net/10399/566.

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Oeveren, Cornelis Adriaan Jan Hubertus van. "5-Alkoxy-2(5H)-furanones in asymmetric synthesis." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 1996. http://irs.ub.rug.nl/ppn/293039712.

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Just, Ziwei W. "Synthesis of 2(3H)-furanones via electrophilic cyclization." [Ames, Iowa : Iowa State University], 2007.

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Hollingworth, Gregory John. "Multifunctional reagents and 2(5H)-Furanones in organic synthesis." Thesis, University of Bristol, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317695.

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Toum, Valérie. "Réactivité d'énaminoesters : synthèse de 4-amino-2(5H)-furanones fonctionnalisées." Paris 6, 2010. http://www.theses.fr/2010PA06A340.

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Les pipéridines sont des structures présentes dans de nombreux alcaloïdes à intérêt biologique. Dans ce contexte, nous avons étudié la réaction d’aza-annélation d’énaminoesters, ce qui nous a permis d’obtenir des dérivés de type pipéridines mono- et bicycliques polyfonctionnelles. Les résultats de la réaction d’aza-annélation d’énaminoesters bromés nous a permis de mettre au point une synthèse efficace de 4-amino-2(5H)-furanones, ou tétronamides, intermédiaires importants dans la synthèse de nombreux produits naturels. Une étude mécanistique a été réalisée et différents intermédiaires ont été
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Edaan, Esra. "Enantioselective syntheses of 2,3-dihydro-4h-pyran-4-ones and 3(2h)-furanones." Thesis, University College London (University of London), 2005. http://discovery.ucl.ac.uk/1444652/.

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This thesis concerns the construction of 2,3-dihydro-4r7-pyran-4-one and 3(2//)-furanone ring systems by mercury(II)-catalysed reactions, or by more conventional cyclisations, and the potential of such reactions for the synthesis of natural products. Chapter one provides a literature survey of reactions permitting the construction of 2,3-dihydro-4/7-pyran-4-one and 3(2//)-furanone ring systems background literature to relevant natural products is also provided, such as polyether antibiotics, carbohydrates and antitumer agents. Chapter two describes the application of mercury(II)-catalysed cycl
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Comte, Gilles. "Structure de glycosides originaux isolés de Juniperus phoenicae L. (cupressacées) : norterpenes, furanones et phenylpropanes." Limoges, 1996. http://www.theses.fr/1996LIMO303C.

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Racamonde, Villanueva Marta. "Síntesi de la (+)-lineatina per mitjà de fotocicloaddicions d'acetilè o anàlegs a 2(5H)-furanones." Doctoral thesis, Universitat Autònoma de Barcelona, 2004. http://hdl.handle.net/10803/3197.

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Alibés, Arqués Ramon. "Síntesi total de (+)-i(-)-grandisol. Fotocicloaddició (2+2) diastereoselectiva de 2(5H)-furanones a alquens." Doctoral thesis, Universitat Autònoma de Barcelona, 1993. http://hdl.handle.net/10803/32150.

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Books on the topic "Furanones"

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Slaughter, J. C. 4-Hydroxy-furanone derivatives as new indicators of malt quality. Home-Grown Cereals Authority, 2000.

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2

Daniel, F. B. Induction of gastrointestinal tract nuclear anomalies in B6C3F1 mice by 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone and 3,4-(dichloro)-5-hydroxy-2(5H)-furanone, mutagenic byproducts of chlorine disinfection. U.S. Environmental Protection Agency, 1992.

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3

Cooper, Vincent Brett. 3,5-Cylic carbonate esters of furanose ring structures, their preparation and some of their reactions. University of Birmingham, 1996.

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Långvik, Vivi-Ann. Formation of the strong mutagen 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone, MX, by chlorination of aromatic model compounds and of fractions of humic water. Åbo Akademi University Press, 1994.

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5

Jong, Johannes Cornelis de. Asymmetric Diels-Alder reactions with 5-methyloxy-2(5H)-furanones. 1991.

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6

Mattauch, Anne-Katrin. Synthese optisch aktiver, überbrückter Desoxy-Furanosen und Desoxy-Disaccharide. 1995.

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7

Lorenzo, María Luisa Ruiz. Determinación y Evaluación de Las Emisiones de Dioxinas y Furanos en la Producción de Cemento en España. Universidad Complutense de Madrid, Servicio de Publicaciones, 2011.

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Book chapters on the topic "Furanones"

1

de Nys, R., M. Givskov, N. Kumar, S. Kjelleberg, and P. D. Steinberg. "Furanones." In Antifouling Compounds. Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/3-540-30016-3_2.

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Ho, Kitty K. K., Samuel K. Kutty, Daniel Chan, Renxun Chen, Mark D. P. Willcox, and Naresh Kumar. "Development of Fimbrolides, Halogenated Furanones and their Derivatives as Antimicrobial Agents." In Antibacterial Surfaces. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-18594-1_8.

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Meier, J. R., A. B. DeAngelo, F. B. Daniel, et al. "Genotoxic and Carcinogenic Properties of Chlorinated Furanones: Important by-Products of Water Chlorination." In Genetic Toxicology of Complex Mixtures. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5850-3_15.

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Rouseff, R., K. Goodner, H. Nordby, and M. Naim. "Comparison of HPLC and GC-MS Analysis of Furans and Furanones in Citrus Juices." In ACS Symposium Series. American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0705.ch018.

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Miller, R. D., W. Theis, G. Heilig, and S. Kirchmeyer. "The Generation and Rearrangement of 2-Diazocarbonyl Cyclobutanones: The Formation of 5-Spirocyclopropyl-2 (5h) Furanones." In Strain and Its Implications in Organic Chemistry. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0929-8_16.

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Pepperman, A. B., and H. G. Cutler. "Plant-Growth-Inhibiting Properties of Some 5-Alkoxy-3-methyl-2(5H)-furanones Related to Strigol." In ACS Symposium Series. American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0443.ch023.

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Bährle-Rapp, Marina. "Dimethylhydroxy Furanone." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3127.

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Kremer, Florian, Benedikt Heuser, and Stefan Pischinger. "Furanoids." In Biofuels from Lignocellulosic Biomass. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527685318.ch6.

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Krishnamurthy, Ramanarayanan, Tammy Campbell, and Eun-Kyong Kim. "Furanose." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_607-4.

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Krishnamurthy, Ramanarayanan, Tammy Campbell, and Eun-Kyong Kim. "Furanose." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_607.

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Conference papers on the topic "Furanones"

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Lönn-Stensrud, J., T. Benneche, and A. Aa Scheie. "Furanones and Thiophenones in Control of Staphylococcus epidermidis Biofilm Infections?" In Proceedings of the International Conference on Antimicrobial Research (ICAR2010). WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814354868_0030.

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Irie, Takayuki, Tokiko Asami, Ayako Sawa, et al. "Abstract A180: Discovery of furanone derivatives as novel Cdc7 inhibitors with anti-tumor activity." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; November 5-9, 2015; Boston, MA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1535-7163.targ-15-a180.

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Siqueira, Ligia, João Assunção, Maria Tominaga, Lady Meneses, Nilson Soares, and Sergio Almeida. "EMISSÕES DE DIOXINAS E FURANOS NA PRODUÇÃO DE CARVÃO VEGETAL EM FORNOS RUDIMENTARES." In XIV Safety, Health and Environment World Congress. Science and Education Research Council (COPEC), 2014. http://dx.doi.org/10.14684/shewc.14.2014.222-227.

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Castro, Jose Adilson de, Aneliza Porto Gonçalves, and Alexandre Jose da Silva. "ESTUDO DE TECNICAS DE RECIRCULAÇÃO DO GÁS DO LEITO DE SINTERIZAÇÃO VISANDO DIMINUIR A EMISSÃO DE DIOXINAS E FURANOS." In 37º Redução e 8º Minério de Ferro. Editora Blucher, 2007. http://dx.doi.org/10.5151/2594-357x-12908.

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Reports on the topic "Furanones"

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Naim, Michael, Gary R. Takeoka, Haim D. Rabinowitch, and Ron G. Buttery. Identification of Impact Aroma Compounds in Tomato: Implications to New Hybrids with Improved Acceptance through Sensory, Chemical, Breeding and Agrotechnical Techniques. United States Department of Agriculture, 2002. http://dx.doi.org/10.32747/2002.7585204.bard.

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The tomato, a profitable vegetable crop in both the USA and Israel, has benefited significantly from intensive breeding efforts in both countries, and elsewhere (esp. Holland). : Modem hybrids are highly prolific and resistant to a variety of major pests. They produce attractive, firm fruit for both processing and fresh-marketing. In all cases, however, reduction in flavor and aroma have occurred concomitantly with the increase in yield. Sugars-acids ratio dominate fruit taste, whereas aroma volatiles (potent at minute ppb and ppt levels) contribute to the total characteristic tomato flavor. A
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