Literatura académica sobre el tema "Hydrazene"
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Artículos de revistas sobre el tema "Hydrazene"
Ibtehal K. Abdullah y Meaad K. Buniya. "Preparation and Identification of some heterocyclic compounds from cyano compounds". Tikrit Journal of Pure Science 20, n.º 5 (10 de febrero de 2023): 96–105. http://dx.doi.org/10.25130/tjps.v20i5.1245.
Texto completoEkram Abdullah Basheer, Kalid Matny Al-jaanaby y Feras Shauki Al-joboury. "Synthesis a Number of Heterocyclic Compounds Derived From Levofloxacin". Tikrit Journal of Pure Science 20, n.º 5 (10 de febrero de 2023): 84–95. http://dx.doi.org/10.25130/tjps.v20i5.1244.
Texto completoAgili, Fatimah. "Novel Hydrazide Hydrazone Derivatives as Antimicrobial Agents: Design, Synthesis, and Molecular Dynamics". Processes 12, n.º 6 (22 de mayo de 2024): 1055. http://dx.doi.org/10.3390/pr12061055.
Texto completoKaur, Aneet Kamal, Renu Bala, Poonam Kumari, Sumit Sood y Karan Singh. "Microwave Assisted Vilsmeier-Haack Reaction on Substituted Cyclohexanone Hydrazones: Synthesis of Novel 4,5,6,7-Tetrahydroindazole Derivatives". Letters in Organic Chemistry 16, n.º 3 (11 de febrero de 2019): 170–75. http://dx.doi.org/10.2174/1570178615666180917101637.
Texto completoPrateeptongkum, Saisuree, Nongnaphat Duangdee y Wiratchanee Mahavorasirikul. "Evaluation of Cytotoxicity and Apoptosis Induced by Coumarin Hydrazide-Hydrazone Derivatives in Human Hepatocellular Carcinoma Cell Line". Trends in Sciences 21, n.º 7 (1 de mayo de 2024): 7628. http://dx.doi.org/10.48048/tis.2024.7628.
Texto completoAlheety, Nuaman. "Synthesis, Characterization and Antimicrobial Activity Study of Some New Substituted Benzoxazole Derivatives". Baghdad Science Journal 16, n.º 3 (1 de septiembre de 2019): 616. http://dx.doi.org/10.21123/bsj.2019.16.3.616.
Texto completoPopiołek, Łukasz. "Updated Information on Antimicrobial Activity of Hydrazide–Hydrazones". International Journal of Molecular Sciences 22, n.º 17 (30 de agosto de 2021): 9389. http://dx.doi.org/10.3390/ijms22179389.
Texto completoAl-Shiekh, Mariam A., Hanady Y. Medrassi, Mohamed H. Elnagdi y Ebtisam A. Hafez. "Substituted Hydrazonals as Building Blocks in Heterocyclic Synthesis: A New Route to Arylhydrazonocinnolines". Journal of Chemical Research 2007, n.º 7 (julio de 2007): 432–36. http://dx.doi.org/10.3184/030823407x234617.
Texto completoAvdeenko, A. P., S. A. Konovalova, I. Yu Yakymenko, V. M. Baumer, S. V. Shishkina y V. V. Pirozhenko. "Interaction of 4-{[(tolyl(methane)sulphonyl)oxy]imino}cyclohexa-2,5-dien-1-ones with N-nucleophiles". Voprosy Khimii i Khimicheskoi Tekhnologii, n.º 1 (enero de 2021): 3–11. http://dx.doi.org/10.32434/0321-4095-2021-134-1-3-11.
Texto completoWu, Shouting, Xi Liang, Fang Luo, Hua Liu, Lingyi Shen, Xianjiong Yang, Yali Huang et al. "Synthesis, Crystal Structure and Bioactivity of Phenazine-1-carboxylic Acylhydrazone Derivatives". Molecules 26, n.º 17 (1 de septiembre de 2021): 5320. http://dx.doi.org/10.3390/molecules26175320.
Texto completoTesis sobre el tema "Hydrazene"
Guevrekian, Soghomoniantz Marina. "Synthèse de nouvelles hydrazones dérivées d'hydrazines disubstituées en position 1 : étude de leurs propriétés antibactériennes, de leur cytotoxicité sur deux espèces d'algues et de leur toxicité sur les alevins de truites". Paris 7, 1985. http://www.theses.fr/1985PA07F059.
Texto completoBelkheiri, Nadji. "Dérivés phénoliques à activités antiathérogènes". Toulouse 3, 2010. http://thesesups.ups-tlse.fr/961/.
Texto completoCardiovascular disease (CVD) are the leading cause of mortality and morbidity in industrialized countries. It has been clearly shown that peroxidation of lipoproteins, mainly low density lipoprotein (LDL), is a critical stage of a very complex process leading to atherosclerosis. Indeed, the relative increase of reactive oxygen species (ROS) due to oxidative stress, induced by means of oxidized low density lipoprotein (oxLDL), a vascular dysfunction. The phenolics are known for their antioxidant properties, especially their free radical scavengers. On the other hand, the hydrazones are effective scavengers carbonyls. In this context, the work described in this manuscript are focused on the research of new molecules with dual cytoprotective and antioxidant properties vis-à-vis the deleterious action of carbonyls from lipid peroxidation of LDL. Based on previous results of the laboratory, we designed and synthesized a new set of phenolics from the same brick molecular the bisvanilline. Bishydrazones of symmetrical and / or with dissymmetry in this case is a function of vinyl-phosphonate and function hydrazone were prepared and studied. At the same time, from the corresponding monohydrazones syringaldehyde have been synthesized and tested. Initially, the antioxidant and cytoprotective were determined for all the molecules synthesized. The most effective compounds were then tested further to assess the effects of carbonyl scavengers, radical O2°- and NO° cell systems (in vitro). The results show unambiguously that, for the first time, we have synthesized molecules with both antioxidant and carbonyl scavenger effect. Finally, the in vivo activity of the most active compound, was evaluated. In a second step, Physicochemical studies have been conducted to understand the mode of action of these compounds through three potential activities in conjunction with their antiatherogenic properties. These tests were on: -The ability of the compounds synthesized radical scavenging stable DPPH• and ABTS•+. -The complexing properties of these compounds with respect to the Cu metal. -The inhibitory action of the compound most active with respect to the in vitro production of superoxide anion O2- degrees
Zerkout, Saïd. "Synthèse d'hydrazino peptides". Vandoeuvre-les-Nancy, INPL, 1994. http://www.theses.fr/1994INPL052N.
Texto completoHsu, Ivann Hong, Joanna Emerson, Andrew Wong y Phillip Zinsli. "2-HYDROXYETHYL HYDRAZINE AND HYDRAZINE HYDRATE PLANT DESIGN". Thesis, The University of Arizona, 2009. http://hdl.handle.net/10150/192492.
Texto completoHuttenhower, Hillary Anne. "Development of new chemistry for a dual use hydrazine thruster, switchable room temperature ionic liquids, a study of silane grafting to polyethylene and its model compounds, synthesis of the novel hydrazine replacement fuel molecules 1,1-dimethyl-2-[2-azidoethyl]hydrazine and 1,1-dimethyl-2-[2-azidoethyl]hydrazone". Diss., Georgia Institute of Technology, 2010. http://hdl.handle.net/1853/41055.
Texto completoSaalmann, Thomas. "Umwandlung cyclischer Hydrazine". [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=97226888X.
Texto completoLe, Duc Minh. "Nouvelle stratégie d’élaboration de la monométhylhydrazine via le procédé Raschig en utilisant la technologie des microréacteurs : synthèse de la chloramine dans des conditions quasi-stoechiométriques et isolement en une seule étape multifonctionnelle". Thesis, Lyon 1, 2012. http://www.theses.fr/2012LYO10335.
Texto completoThis work, conducted as part of a collaboration with the Safran-Heraklès group, aims at developing a new synthesis concept for the monomethylhydrazine (MMH), by process intensification using microreactor technology. The work was funded by the Rhône-Alpes region in the form of a doctoral fellowship TARGET 2008-2011. The first part of this research aims to study the stability of monochloramine solutions prepared in stoichiometric conditions. This synthesis was carried out continuously, for the first time ever, using microreactor technology. Optimal synthesis conditions as well as a set of security parameters have been established for a fast and secured transfer to industrial scale. The second part, also one of the main objectives of this work, is the extraction, under pressure, of all organic products (mostly MMH and monomethylamine) in the form of one condensed phase by demixing the crude reaction liquors. This phenomenon is related to the existence of a miscibility gap in the liquid ternary system H2O-MMA-NaOH. The optimization of the demixing step requires then the study of different solid-liquid-liquid phase diagrams involved. The last part deals with the chemical engineering aspect of the research. A kinetic modeling of the synthesis of MMH by the Raschig way was used in order to estimate the composition of the synthesis solution. These results and the application of phase diagrams allow the determination of optimal conditions for the isolation step and the establishment of process flow-sheets for the synthesis of MMH
Clavette, Christian. "Synthesis of Beta-Aminocarbonyl Compounds and Hydrazine Derivatives Using Amino- and Imino-Isocyanates". Thesis, Université d'Ottawa / University of Ottawa, 2015. http://hdl.handle.net/10393/32004.
Texto completoVogt, Kirkland W. "Nitridation reactions with hydrazine". Diss., Georgia Institute of Technology, 1994. http://hdl.handle.net/1853/10032.
Texto completoCriton, Thomas. "Systèmes polyazotés énergétiques : stratégie de synthèse, caractérisation et réactivité". Thesis, Lyon, 2019. http://www.theses.fr/2019LYSE1222.
Texto completoHydrazines for propulsion have been identified by REACH regulation as Substances of Very High Concern (SVHC) and their use is therefore threatened. High Energy Density Materials (HEDM) represent a class of polynitrogen compounds with computed energetic performances breaking away from existing technologies. Besides solving toxicity issues thanks to their decomposition in molecular nitrogen, their use would highly simplify launcher’s technologies and decreases their cost. Two candidates have been proposed by the CNES and ArianeGroup to replace hydrazines: triaziridine (N3H3) and tetrazetidine (N4H4). The main goal of this thesis is to develop new methodologies for the synthesis of polynitrogen compounds and to investigate their reactivity to access to original structures such as triaziridine and tetrazetidine. Homologation of simple nitrogen-based compounds with azodicarboxylates enabled us to access new original superior polynitrogen molecules (N3, N4, N5, N6…). Structural evidences of these new polynitrogen backbones have been obtained by X-ray diffraction. Their reactivity by regioselective activation and by oxidation has been studied to access cyclic polynitrogen structures
Libros sobre el tema "Hydrazene"
Schmidt, Eckart W. Hydrazine and its derivatives: Preparation, properties, applications. 2a ed. New York: Wiley-Interscience, 2001.
Buscar texto completoInternational Program on Chemical Safety., ed. Hydrazine. Geneva: World Health Organization, 1987.
Buscar texto completoOrganization, World Health y International Program on Chemical Safety, eds. Hydrazine. Geneva: World Health Organization, 1987.
Buscar texto completoKagaku Busshitsu Hyōka Kenkyū Kikō y Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Hidorajin: Hydrazine. Tōkyō-to Shibuya-ku: Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.
Buscar texto completoPatil, K. C. y Tanu Mimani Rattan, eds. Inorganic Hydrazine Derivatives. Chichester, United Kingdom: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.
Texto completoUnited States. National Aeronautics and Space Administration., ed. The catalysis of hydrazine. Washington, DC: National Aeronautics and Space Administration, 1987.
Buscar texto completoSuzuki, M. Decomposition of hydrazine by high frequency glow electrical discharges. Washington, DC: National Aeronautics and Space Administration, 1988.
Buscar texto completoInternational Program on Chemical Safety., International Labour Organisation, United Nations Environment Programme y World Health Organization, eds. Hydrazine health and safety guide. Geneva: World Health Organization, 1991.
Buscar texto completoCanada, Canada Health. Hydrazine sulphate: An information package. Toronto: Health Canada, 1996.
Buscar texto completoCanadian Breast Cancer Research Initiative., ed. Hydrazine sulphate: An information package. Toronto: Canadian Breast Cancer Research Initiative, 1996.
Buscar texto completoCapítulos de libros sobre el tema "Hydrazene"
Lane, J. D., C. J. Pickett y D. R. Stanley. "From Hydrazine and Coordinated Hydrazines". En Inorganic Reactions and Methods, 116–17. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch86.
Texto completoLane, J. D., C. J. Pickett y D. R. Stanley. "Hydrazine and Substituted Hydrazine Complexes". En Inorganic Reactions and Methods, 100–102. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145227.ch74.
Texto completoAruna, Singanahally T. y K. C. Patil. "Hydrazine Salts". En Inorganic Hydrazine Derivatives, 37–82. Chichester, United Kingdom: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch02.
Texto completoAudrieth, L. F., T. T. Nickles, G. Gibson y R. E. Kirk. "Hydrazine Sulfate". En Inorganic Syntheses, 90–91. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132326.ch31.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of oxovanadium(IV) complex with hydrazone of isonicotinic acid hydrazide". En Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 5, 29–30. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65098-1_7.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of chromium(III) complex with hydrazone of isonicotinic acid hydrazide". En Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 5, 85–86. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65098-1_31.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of manganese(III) complex with hydrazone of isonicotinic acid hydrazide". En Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 5, 218–19. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65098-1_79.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of iron(III) complex with hydrazine of isonicotinic acid hydrazide". En Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 5, 352–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65098-1_125.
Texto completoAudrieth, L. F., T. T. Nickles, G. Gibson y R. E. Kirk. "Recovery of Hydrazine Residues as Hydrazine Dihydro Chloride or Hydrazine Sulfate". En Inorganic Syntheses, 92–94. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132326.ch32.
Texto completoRattan, Tanu Mimani y K. C. Patil. "Hydrazine and Its Inorganic Derivatives". En Inorganic Hydrazine Derivatives, 1–36. Chichester, United Kingdom: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118693599.ch01.
Texto completoActas de conferencias sobre el tema "Hydrazene"
Antonijević, Marko, Žiko Milanović, Dušica Simijonović, Zoran Marković y Snežana Marković S. Zoran. "ANTIOXIDATIVE POTENCY AND RADICAL SCAVENGING ACTIVITY OF SELECTED COUMARIN-HYBRIDS". En 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac,, 2021. http://dx.doi.org/10.46793/iccbi21.458a.
Texto completoPopusoi, Ana, Nicanor Barba y Aurelian Gulea. "Synthesis of 1,3-Phenyl(Pyridyl)propenones with thiosemicarbazidic groups". En Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab03.
Texto completoBruckdorfer, Thomas, Pavel S. Chelushkin, Ksenia V. Polyanichko, Maria Leko, Marina Dorosh y Sergey V. Burov. "Convenient method of peptide hydrazide synthesis using a new hydrazone resin". En 35th European Peptide Symposium. Prompt Scientific Publishing, 2018. http://dx.doi.org/10.17952/35eps.2018.084.
Texto completoBranković, Jovica, Zorica D. Petrović y Vladimir P. Petrović. "Phenolic N-acyl hydrazone derivatives: In silico assessment of potential antibacterial activity against selected G+ and G- strains". En 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.491b.
Texto completoGuo, Hong, Pengdi Ren, Xiaoyu Zhang, Guangxiong Chen y Yi Ye. "Fretting Wear Behavior of NC30Fe in Distilled Water and Hydrazine Solution". En 2013 21st International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icone21-15879.
Texto completoWon, Hui-Jun, Jung-Soon Park, Chong-Hun Jung, Sang-Yoon Park, Wang-Kyu Choi y Jei-Kwon Moon. "A Reductive Dissolution Study of Magnetite". En ASME 2013 15th International Conference on Environmental Remediation and Radioactive Waste Management. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icem2013-96101.
Texto completoPathak, Anisha y Banshi Dhar Gupta. "Palladium nanoparticles decorated MWCNTs engraved in polypyrrole matrix for the sensitive detection of hydrazine based on FOSPR". En JSAP-OSA Joint Symposia. Washington, D.C.: Optica Publishing Group, 2017. http://dx.doi.org/10.1364/jsap.2017.6a_a410_7.
Texto completoDomae, Masafumi, Hirotaka Kawamura, Daisuke Akutagawa, Kenji Hisamune, Yosuke Katsumura y Yusa Muroya. "Corrosion Test of 304 Stainless Steel in Hydrazine and Methanol Solutions at 320°C Under Gamma-Irradiation and Gamma Radiolysis of Hydrazine and Methanol". En 18th International Conference on Nuclear Engineering. ASMEDC, 2010. http://dx.doi.org/10.1115/icone18-29281.
Texto completoBranković, Jovica, Vesna Milovanović y Vladimir P. Petrović. "CYCLOOXYGENASE-2 AS „IN SILICO“ TARGET OF PHENOLIC HYDRAZONE- TYPE DERIVATIVES". En 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.324b.
Texto completoAbdulhamid, Hakim, Jérôme Limido, Paul Deconinck y Christian Puillet. "Experimental Validation of Hydrazine Reaction Model Through Hypervelocity Impact Tests". En 2022 16th Hypervelocity Impact Symposium. American Society of Mechanical Engineers, 2022. http://dx.doi.org/10.1115/hvis2022-1.
Texto completoInformes sobre el tema "Hydrazene"
Garcia, B. y D. Chavez. Shock compression of liquid hydrazine. Office of Scientific and Technical Information (OSTI), enero de 1995. http://dx.doi.org/10.2172/105881.
Texto completoKarraker, D. G. The Oxidation of Hydrazine by Nitric Acid. Office of Scientific and Technical Information (OSTI), julio de 2001. http://dx.doi.org/10.2172/784248.
Texto completoThiem, Terry L., Jason Brown, Johnathan Kiel, Eric Holwitt y Gerald J. O'Brien. The Chemical and Biochemical Degradation of Hydrazine. Fort Belvoir, VA: Defense Technical Information Center, enero de 1997. http://dx.doi.org/10.21236/ada333221.
Texto completoKarraker, D. G. Cu(II) - Catalyzed Hydrazine Reduction of Ferrous Nitrate. Office of Scientific and Technical Information (OSTI), octubre de 2001. http://dx.doi.org/10.2172/787806.
Texto completoHARDING LAWSON ASSOCIATES NOVATO CA. Hydrazine Blending and Storage Facility, Interim Response Action. Fort Belvoir, VA: Defense Technical Information Center, enero de 1991. http://dx.doi.org/10.21236/ada273439.
Texto completoKarraker, D. G. The Iron-Catalyzed Oxidation of Hydrazine by Nitric Acid. Office of Scientific and Technical Information (OSTI), julio de 2001. http://dx.doi.org/10.2172/783929.
Texto completoZube, Dieter M. y Dan Fye. Low Bus Voltage Hydrazine Arcjet System for Geostationary Satellites. Fort Belvoir, VA: Defense Technical Information Center, julio de 1998. http://dx.doi.org/10.21236/ada408186.
Texto completoDeLorenzo, Robert J. The Effects of Hydrazines on Neuronal Excitability. Fort Belvoir, VA: Defense Technical Information Center, octubre de 1993. http://dx.doi.org/10.21236/ada290120.
Texto completoBertrand, Guy. Ammonia and hydrazine. Transition-metal-catalyzed hydroamination and metal-free catalyzed functionalization. Office of Scientific and Technical Information (OSTI), junio de 2012. http://dx.doi.org/10.2172/1253630.
Texto completoHARDING LAWSON ASSOCIATES NOVATO CA. Hydrazine Blending and Storage Facility, Interim Response Action Implementation. Final Safety Plan. Fort Belvoir, VA: Defense Technical Information Center, agosto de 1989. http://dx.doi.org/10.21236/ada271897.
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