Literatura académica sobre el tema "Pyrazole-4"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "Pyrazole-4".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "Pyrazole-4"
Abaszadeh, Mehdi, Hassan Sheibani y Kazem Saidi. "The Condensation of (Chlorocarbonyl)phenyl Ketene with Bisnucleophiles. Synthesis of 4-Hydroxy-5-phenylpyro-[2,3-c]pyrazol-6-ones and Formation of Pyrazolo[1,2-a]pyrazole-triones by Hydrogen Exchange in Unstable Mesoionic Compounds". Australian Journal of Chemistry 63, n.º 1 (2010): 92. http://dx.doi.org/10.1071/ch09344.
Texto completoHartwig de Oliveira, Daniela, Fernanda Severo Sabedra Sousa, Paloma Taborda Birmann, Ana Paula Pesarico, Diego Alves, Raquel Guimarães Jacob y Lucielli Savegnago. "Evaluation of antioxidant activity and toxicity of sulfur- or selenium-containing 4-(arylchalcogenyl)-1H-pyrazoles". Canadian Journal of Physiology and Pharmacology 98, n.º 7 (julio de 2020): 441–48. http://dx.doi.org/10.1139/cjpp-2019-0356.
Texto completoAlsayari, Abdulrhman, Abdullatif Bin Muhsinah, Yahya I. Asiri, Jaber Abdullah Alshehri, Yahia N. Mabkhot, Mohammad Y. Alfaifi, Serag Eldin I. Elbehairi, Mater H. Mahnashi y Mohd Zaheen Hassan. "Arylhydrazono/Aryldiazenyl Pyrazoles: Green One-Pot Solvent-Free Synthesis and Anticancer Evaluation". Letters in Organic Chemistry 17, n.º 10 (17 de noviembre de 2020): 772–78. http://dx.doi.org/10.2174/1570178617666200320104923.
Texto completoAndicsová, Anita, Angelika Lásiková, Marek Fronc, Jozef Kožíšek y Daniel Végh. "3-(2-Heteroaryl)-pyrazolotetrazoles – a subunits for losartan-like structures". Acta Chimica Slovaca 5, n.º 2 (1 de noviembre de 2012): 220–24. http://dx.doi.org/10.2478/v10188-012-0033-z.
Texto completoSrinivasa Reddy, T., Hitesh Kulhari, V. Ganga Reddy, A. V. Subba Rao, Vipul Bansal, Ahmed Kamal y Ravi Shukla. "Synthesis and biological evaluation of pyrazolo–triazole hybrids as cytotoxic and apoptosis inducing agents". Organic & Biomolecular Chemistry 13, n.º 40 (2015): 10136–49. http://dx.doi.org/10.1039/c5ob00842e.
Texto completoLindsay-Scott, Peter J. y Eloise Rivlin-Derrick. "Regiocontrolled Synthesis of 6,7-Dihydro-4H-pyrazolo[5,1-c][1,4]oxazines". Synthesis 52, n.º 01 (8 de octubre de 2019): 105–18. http://dx.doi.org/10.1055/s-0037-1610734.
Texto completoRamadan, El Sayed, Essam M. Sharshira, Ramadan I. El Sokkary y Noussa Morsy. "Synthesis and antimicrobial evaluation of some heterocyclic compounds from 3-aryl-1-phenyl-1H-pyrazole-4-carbaldehydes". Zeitschrift für Naturforschung B 73, n.º 6 (27 de junio de 2018): 389–97. http://dx.doi.org/10.1515/znb-2018-0009.
Texto completoDeacon, Glen B., Peter C. Junk y Aron Urbatsch. "Lanthanoid and Alkaline Earth Complexes Involving New Substituted Pyrazolates". Australian Journal of Chemistry 65, n.º 7 (2012): 802. http://dx.doi.org/10.1071/ch12069.
Texto completoLam, Linh, Sang H. Park y Joseph Sloop. "Synthesis and Characterization of 3-Methyl-1-(4-(trifluoromethyl)phenyl)indeno [1,2-c]pyrazol-4(1H)-one". Molbank 2022, n.º 4 (7 de noviembre de 2022): M1483. http://dx.doi.org/10.3390/m1483.
Texto completoRizk, Sameh, Ismail M. Awheda y Fathi A. Smida. "Synthesis and DFT Study of Newly Schiff Base and Fused Heterocyclic Compounds as Antibacterial Agent". JOURNAL OF ADVANCES IN CHEMISTRY 16 (7 de noviembre de 2019): 5395–403. http://dx.doi.org/10.24297/jac.v16i0.8499.
Texto completoTesis sobre el tema "Pyrazole-4"
Karahan, Dag Fulya. "Synthesis Of 5-ferrocenyl-4-((4-nitrophenyl)sulfenyl)-1h-pyrazoles By Electrophilic Cyclization". Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613443/index.pdf.
Texto completoDemirci, Deniz. "Synthesis Of 4-phenylselenyl-1h-pyrazoles By Electrophilic Cyclization". Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613910/index.pdf.
Texto completoBarus, M. M. "А new approach to the preparation of 4-difluoromethyl-1Н-pyrazole-3-carboxylic acids". Thesis, БДМУ, 2022. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/19532.
Texto completoYazici, Ceyda. "Synthesis Of 4-iodopyrazole Derivatives". Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609750/index.pdf.
Texto completoC for 5 h. Finally, acetylenic phenyl hydrazone derivatives were subjected to electrophilic cyclization by treating with excess molecular iodine at 80 °
C for 3 h. Although electrophilic cyclization is commonly used in organic chemistry, it has not been employed for the cyclization of acetylenic phenyl hydrazones to pyrazole derivatives. Under optimized conditions, these reactions afforded 1-aryl-5-alkyl/aryl-4-iodopyrazole derivatives in moderate to good yields as the single or the major product of the reactions. In some cases, 1-aryl-5-alkyl/arylpyrazole derivatives resulted from these reactions as minor products. In conclusion, 4-iodopyrazole derivatives were synthesized for the first time directly from acyclic starting materials, ,-acetylenic phenylhydrazones and iodine, via electrophilic cyclization.
Cottineau, Bertrand. "Contribution à l'étude du 3-hydroxy-1H-pyrazole-4-carboxylate d'éthyle : application à la synthèse de composés antidiabétiques". Orléans, 2002. http://www.theses.fr/2002ORLE2014.
Texto completoKivrak, Arif. "Development Of New Methods For The Synthesis Of Pyrazoles, 4-iodopyrazoles, Isoxazoles And 1,2,4-oxadiazoles". Phd thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12612945/index.pdf.
Texto completo,&beta
-alkynic hydrazones by molecular iodine and copper iodide were investigated as new ways for the synthesis of 4-iodopyrazoles and pyrazoles, respectively. Initially, &alpha
,&beta
-alkynic hydrazones were prepared by the reactions of propargyl aldehydes and ketones with hydrazines. Then &alpha
,&beta
-alkynic hydrazones were treated with molecular iodine in the presence of NaHCO3, which afforded 4-iodopyrazoles in good to excellent yields. Subsequently, the same reactions were carried out with CuI in the presence of NEt3, which furnished corresponding pyrazoles in good yields. Moreover, ferrocenyl-substituted 4-iodopyrazoles and pyrazole derivatives were synthesized from corresponding
Toto, Patrick. "Contribution à l'étude du 1H-pyrazole-4-carboxylate d'éthyle et de ses dérivés : application à la synthèse de nouveaux hétérocycles polycondensés". Orléans, 2004. http://www.theses.fr/2004ORLE2001.
Texto completoDesalegn, Nebiyou. "Kinetic Studies Of The Thermolysis Of 3-Halogenated-4,5-Dihydro-3h-Pyrazoles". Digital Archive @ GSU, 2005. http://digitalarchive.gsu.edu/chemistry_theses/1.
Texto completoPiovesan, Luciana Almeida. "Síntese de novos heterociclos a partir do ácido levulínico". Universidade Federal de Santa Maria, 2009. http://repositorio.ufsm.br/handle/1/4233.
Texto completoThe synthesis of new compounds alkyl 3-azolyl propanoate e alkyl 3-azolyl propanoic acid structurally analogues to gamma-aminobutiric acid (GABA) is reported. One more time using the acetal acylation method, now the acetal derivative of 4-oxopentanoic acid (levulinic acid), the methyl 4,4- dimethoxypentanoate, were obtained the precursors methyl 7,7,7-trifluoro[chloro]-4- methoxy-6-oxo-heptenoates, 1,3-dieletrophilic precursor with alcanoate substituent. Are presented efficient and regioespecific synthetic routes from reactions of cyclocondensation [3+2] among 1,3-dieletrofilic precursors with hydroxylamine and different hydrazines, until training isoxazoles and pyrazoles, functionalized with the side chain alkyl propanoate or propanoic acid. Simultaneously to the formation of heterocycles, were studied the hydrolysis reaction of trichloromethyl group and transesterification reaction of methyl propanoate, in the same reactional medium. All products are novel, presenting a good to excellent yields, high purity and the structures were assigned by 1H NMR, 13C NMR and mass spectrometry.
A síntese de novos compostos 3-azolil-propanoatos de alquila e 3-azolilácidos propanóicos, análogos estruturalmente ao ácido gama-aminobutírico (GABA) é relatada. Novamente aplicando o método de acilação de acetais, agora ao acetal derivado do ácido 4-oxopentanóico (ácido levulínico), o 4,4-dimetoxipentanoato de metila, foram obtidos os precursores 7,7,7-triflúor[cloro]-4-metoxi-6-oxo-heptenoatos de metila, precursores 1,3-dieletrofílicos com o substituinte alcanoato. São apresentadas rotas sintéticas eficientes e regioespecíficas a partir de reações de ciclocondensação [3+2] entre os precursores 1,3-dieletrofílicos, com hidroxilamina e hidrazinas diferentes, até a formação de isoxazóis e pirazóis, funcionalizados com a cadeia lateral propanoato de alquila ou ácido propanóico. Simultaneamente à formação dos heterociclos, foram estudadas as reações de hidrólise do grupamento triclorometila e hidrólise ou transesterificação do propanoato de metila, no mesmo meio de reação. Todos os produtos obtidos são inéditos, apresentando rendimentos de bons a excelentes e pureza alta e suas estruturas foram atribuídas por RMN1H e 13C e por espectrometria de massas.
Oleksik, Laurence. "Methodology for the synthesis of 4 or 5-substituted-3-perfluoroalkyl pyrazoles". Thesis, University of Leicester, 2004. http://hdl.handle.net/2381/30087.
Texto completoCapítulos de libros sobre el tema "Pyrazole-4"
Lynch, Michael P., James R. Beck, Eddie V. P. Tao, James Aikins, George E. Babbitt, John R. Rizzo y T. William Waldrep. "1-Alkyl-5-cyano-1H-pyrazole-4-carboxamides". En ACS Symposium Series, 144–57. Washington, DC: American Chemical Society, 1991. http://dx.doi.org/10.1021/bk-1991-0443.ch012.
Texto completoBährle-Rapp, Marina. "4,5-Diamino-1-((4-Chlorophenyl)Methyl)-1H-Pyrazole-Sulfate". En Springer Lexikon Kosmetik und Körperpflege, 151. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2833.
Texto completoLynch, Michael P., Stephen A. Ackmann, Dale R. Heim, George E. Davis, Michael A. Staszak, James R. Beck, Edward E. Tschabold y Fred L. Wright. "Synthesis and Gametocidal Activity of 1-Aryl-5-(aminocarbonyl)-1H-pyrazole-4-carboxylic Acids". En Synthesis and Chemistry of Agrochemicals III, 200–211. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch019.
Texto completoShao, Xia, Keunsam Jang y Peter J. H. Scott. "Synthesis of 1-(2,4-Dichlorophenyl)-4-Cyano-5-(4-[11C]methoxyphenyl)-N-(Piperidin-1-yl)-1H-Pyrazole-3-Carboxamide ([11C]OMAR)". En Radiochemical Syntheses, 73–80. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118834114.ch8.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of dinuclear bis(μ-3-pyridin-2yl-1, 2, 4-triazolato) copper(II) compound containing pyrazole as CO-ligand". En Magnetic Properties of Paramagnetic Compounds, 252–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_115.
Texto completoHamper, Bruce C., Kindrick L. Leschinsky, Deborah A. Mischke y S. Douglas Prosch. "Chiral 3-Aryl-4-halo-5-(trifluoromethyl)pyrazoles". En ACS Symposium Series, 272–81. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-2000-0746.ch019.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of μ3-OMe bridged tricopper(II) chloro complex with substituted pyrazole". En Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4, 722–24. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_291.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of μ3-OMe bridged tricopper(II) bromo complex with substituted pyrazole". En Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4, 725–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_292.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of cobalt(II) complex of 4-(sulfonylazido)phenylazo-pyrazolone". En Magnetic Properties of Paramagnetic Compounds, 943–44. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_502.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of cobalt(II) complex of 4-(sulfonylazido)phenylazo-pyrazolone". En Magnetic Properties of Paramagnetic Compounds, 945–46. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_503.
Texto completoActas de conferencias sobre el tema "Pyrazole-4"
Hyuga, H., C. Goto, Y. Okazaki, A. Harada, S. Mitsumoto, K. Kamiyama y S. Umegaki. "An Organic Crystal 3,5-dimethyl-1-(4-nitrophenyl)pyrazole for Compact Visible Light-sources". En Compact Blue-Green Lasers. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/cbgl.1993.cwa.2.
Texto completoPrasad, T. N. Mahadeva, B. N. Lakshminarayana, Ebraheem Abdu Musad, M. A. Sridhar, K. M. Lokanath Rai, J. Shashidhara Prasad, Alka B. Garg, R. Mittal y R. Mukhopadhyay. "Synthesis and X-ray Crystallographic Studies of ethyl 3-methyl5-(methylthio)-1H-pyrazole-4-carboxylate". En SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3605798.
Texto completoFauzi'ah, Lina y Tutik Dwi Wahyuningsih. "Synthesis of 3-(4’-nitrophenyl)-4,5-dihydro pyrazole-based and its in-vitro antibacterial test". En PROCEEDING OF INTERNATIONAL CONFERENCE ON FRONTIERS OF SCIENCE AND TECHNOLOGY 2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0103273.
Texto completoChandra, N. Srikantamurthy, E. A. Jithesh Babu, K. B. Umesha y M. Mahendra. "Synthesis and crystal structure studies of ethyl 5-methyl-1, 3-diphenyl-1H-pyrazole-4-carboxylate". En SOLID STATE PHYSICS: Proceedings of the 58th DAE Solid State Physics Symposium 2013. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4872901.
Texto completoMedvedev, Michail, Michail Elinson y Alexey Ilovaisky. "Green approach to the design of functionalized medicinally privileged 4-aryl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile scaffold !" En The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00580.
Texto completoMishra, Ashutosh y Garima Jain. "XRD and xanes studies of copper complexes using (diethyl 4-amino-1-phenyl-1H-pyrazole-3,5 dicarboxylate) as ligand". En PROCEEDING OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN APPLIED PHYSICS AND MATERIAL SCIENCE: RAM 2013. AIP, 2013. http://dx.doi.org/10.1063/1.4810475.
Texto completoKoalla, Rajesh, Chandan Ghorui, Shivanand Mangali, Naveen Periketi y A. K. Chaudhary. "Measurement of Refractive index and Absorption coefficient of 3, 4, 5 -Trinitro 1-H Pyrazole using Terahertz Time-domain Spectroscopy". En Frontiers in Optics. Washington, D.C.: OSA, 2021. http://dx.doi.org/10.1364/fio.2021.jw7a.58.
Texto completoNikalje, Anna Pratima, Julio Seijas Vázquez, M. Pilar Vazquez-Tato y Urja Nimbalkar. "Ionic liquid [Et3NH][HSO4]catalyslyzed multicomponent synthesis of 6 amino-4-(Substituted phenyl)-3-methyl-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile ". En The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-f011.
Texto completoKumar, Rakesh, Neha Yadav, Jyoti Arora y Ashok K. Prasad. "Synthesis of chiral 4-pyrazolyl dihydropyridines and their enantiomeric separation". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013101521523.
Texto completoJean Pierre, Bazureau, Camille Dago, Lou-Anna Voli, Thierry Roisnel, Christophe Brigaudeau, Yves-Alain Békro, Janat Mamybékova y Olivier Mignen. "A Practical Access to New Pyrazole SKF-96365 Analogues as Potential Store-Operated Calcium Entry (SOCE) Inhibitors". En 4th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05618.
Texto completoInformes sobre el tema "Pyrazole-4"
Schmidt, R. D., G. S. Lee, P. F. Pagoria, A. R. Mitchell y R. Gilardi. Synthesis and Properties of a New Explosive, 4-Amino-3,5-Dinitro-lH-Pyrazole (LLM-116). Office of Scientific and Technical Information (OSTI), mayo de 2001. http://dx.doi.org/10.2172/15005359.
Texto completo