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Artykuły w czasopismach na temat "Pyrazoles"
Alsayari, Abdulrhman, Abdullatif Bin Muhsinah, Yahya I. Asiri, Jaber Abdullah Alshehri, Yahia N. Mabkhot, Mohammad Y. Alfaifi, Serag Eldin I. Elbehairi, Mater H. Mahnashi i Mohd Zaheen Hassan. "Arylhydrazono/Aryldiazenyl Pyrazoles: Green One-Pot Solvent-Free Synthesis and Anticancer Evaluation". Letters in Organic Chemistry 17, nr 10 (17.11.2020): 772–78. http://dx.doi.org/10.2174/1570178617666200320104923.
Pełny tekst źródłaElnagdi, Mohamed Hilmy, Ahmed Hafez Hussien Elghandour, Kamal Usef Sadek i Mahmoud Mohamed Mahfouz Ramiz. "Studies on Condensed Pyrazoles. A New Route for Synthesis of Pyrazolo[4,3-c]pyrazoles". Zeitschrift für Naturforschung B 44, nr 8 (1.08.1989): 951–54. http://dx.doi.org/10.1515/znb-1989-0816.
Pełny tekst źródłaChauhan, Pankaj, Suruchi Mahajan i Dieter Enders. "Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives". Chemical Communications 51, nr 65 (2015): 12890–907. http://dx.doi.org/10.1039/c5cc04930j.
Pełny tekst źródłaLin, Wei-Syuan, i Shigeki Kuwata. "Recent Developments in Reactions and Catalysis of Protic Pyrazole Complexes". Molecules 28, nr 8 (17.04.2023): 3529. http://dx.doi.org/10.3390/molecules28083529.
Pełny tekst źródłaQueiroz, Jaqueline E., Lucas D. Dias, Giuliana M. Vila Verde, Gilberto L. B. Aquino i Ademir J. Camargo. "An Update on the Synthesis and Pharmacological Properties of Pyrazoles Obtained from Chalcone". Current Organic Chemistry 26, nr 2 (styczeń 2022): 81–90. http://dx.doi.org/10.2174/1385272826666220119110347.
Pełny tekst źródłaMilišiūnaitė, Vaida, Rūta Paulavičiūtė, Eglė Arbačiauskienė, Vytas Martynaitis, Wolfgang Holzer i Algirdas Šačkus. "Synthesis of 2H-furo[2,3-c]pyrazole ring systems through silver(I) ion-mediated ring-closure reaction". Beilstein Journal of Organic Chemistry 15 (14.03.2019): 679–84. http://dx.doi.org/10.3762/bjoc.15.62.
Pełny tekst źródłaLam, Linh, Sang H. Park i Joseph Sloop. "Synthesis and Characterization of 3-Methyl-1-(4-(trifluoromethyl)phenyl)indeno [1,2-c]pyrazol-4(1H)-one". Molbank 2022, nr 4 (7.11.2022): M1483. http://dx.doi.org/10.3390/m1483.
Pełny tekst źródłaLindsay-Scott, Peter J., i Eloise Rivlin-Derrick. "Regiocontrolled Synthesis of 6,7-Dihydro-4H-pyrazolo[5,1-c][1,4]oxazines". Synthesis 52, nr 01 (8.10.2019): 105–18. http://dx.doi.org/10.1055/s-0037-1610734.
Pełny tekst źródłaMantzanidou, Martha, Eleni Pontiki i Dimitra Hadjipavlou-Litina. "Pyrazoles and Pyrazolines as Anti-Inflammatory Agents". Molecules 26, nr 11 (5.06.2021): 3439. http://dx.doi.org/10.3390/molecules26113439.
Pełny tekst źródłaWarkentin, John, i John Mck R. Woollard. "Photolysis of 5,5-dibenzyl-Δ3-1,3,4-oxadiazolines". Canadian Journal of Chemistry 75, nr 3 (1.03.1997): 289–307. http://dx.doi.org/10.1139/v97-033.
Pełny tekst źródłaRozprawy doktorskie na temat "Pyrazoles"
Ostache, Nicu-Carmin. "Synthèse et fonctionnalisation de bicycles 5-5 polyazotés : pyrazolo[3,4-d]thiazoles et pyrazolo[3,4-c]pyrazoles". Thesis, Orléans, 2019. http://intranet.univ-orleans.fr/bibliotheques/theses/nicu-cosmin-ostache_3378_vm.pdf/.
Pełny tekst źródłaNitrogen-rich fused bicyclic structures are undisputedly one of the most used scaffolds for therapeutic use.The 5:5 polynitrogenated bicycles are moieties considerably less documented then their 6:6 or 6:5analogues. Despite the pharmacological potential of the pyrazolo[3,4-d]thiazoles and of thepyrazolo[3,4-c]pyrazoles, two examples of such rare families, only few methods of preparation and directfunctionalization of these heterocyclic moieties have been described.In this context, the main goal of our research aims at exploring new routes towards these bicyclic systemsfrom readily available and affordable starting materials. Efficient strategies were developed relying onhydrazine condensations, on intramolecular N-cyclizations, on chemo-selective halogenation and variouscross-coupling reactions. Moreover, the pyrazolo[3,4-d]thiazole entity was fused to a triazapentalenestructure in order to assess the spectroscopic properties
Gormen, Meral. "Synthesis Of Ferrocenyl Substituted Pyrazoles". Master's thesis, METU, 2005. http://etd.lib.metu.edu.tr/upload/3/12606358/index.pdf.
Pełny tekst źródłaEl, Youssoufi Jawad. "Synthèses de pyrazoles benzocyclohepténiques glycosylés". Limoges, 1997. http://www.theses.fr/1997LIMO0027.
Pełny tekst źródłaErvithayasuporn, Vuthichai. "Synthesis and photochemistry of pyrano[2,3-c]pyrazoles". Link to electronic thesis, 2006. http://www.wpi.edu/Pubs/ETD/Available/etd-042006-160619/.
Pełny tekst źródłaERVITHAYASUPORN, VUTHICHAI. "Synthesis and Photochemistry of Pyrano[2,3-c]pyrazoles". Digital WPI, 2006. https://digitalcommons.wpi.edu/etd-theses/228.
Pełny tekst źródłaDesalegn, 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.
Pełny tekst źródłaCooper, David Arthur. "The synthesis and characterization of some molybdenum, rhenium and rhodium complexes incorporating pyrazolylgallate ligands". Thesis, University of British Columbia, 1985. http://hdl.handle.net/2429/24597.
Pełny tekst źródłaScience, Faculty of
Chemistry, Department of
Graduate
Nakhai, Azadeh. "Synthetic studies of nitrogen containing heterocycles, particularly pyrazole and benzotriazine derivatives". Stockholm, 2009. http://diss.kib.ki.se/2009/978-91-7409-687-3/.
Pełny tekst źródłaDemirci, 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.
Pełny tekst źródłaTruong, Phong Minh. "Hexa-aryl/alkylsubstituted Cyclopropanes". Digital Archive @ GSU, 2006. http://digitalarchive.gsu.edu/chemistry_theses/2.
Pełny tekst źródłaKsiążki na temat "Pyrazoles"
Degtev, M. I. Fiziko-khimicheskie svoĭstva antipirina i ego proizvodnykh: Monografii︠a︡. Permʹ: Permskiĭ gos. universitet, 2010.
Znajdź pełny tekst źródłaJacques, Teresa. I : Catalytic Direct C-H Arylation of Pyrazoles. II: Toward Modulation of Neuroplasticity with Small Molecules. [New York, N.Y.?]: [publisher not identified], 2013.
Znajdź pełny tekst źródłaKresinski, Roman Alexander. Tris(pyrazolyl)borate complexes of Group IV metals. Birmingham: University of Birmingham, 1990.
Znajdź pełny tekst źródłaKarim, Mohammed. Composition de quelques pyrazolines: Etude de leur activité biologique. Saarbrücken: Noor Publishing, 2017.
Znajdź pełny tekst źródłaWiley, Richard H., i Paul F. Wiley. Pyrazolones, Pyrazolidones, and Derivatives. Wiley & Sons, Incorporated, John, 2009.
Znajdź pełny tekst źródłaWiley, Richard H., i Paul F. Wiley. Pyrazolones, Pyrazolidones, and Derivatives. Wiley & Sons, Limited, John, 2007.
Znajdź pełny tekst źródłaWiley, Richard H. Pyrazoles and Reduced and Condensed Pyrazoles. Wiley & Sons, Incorporated, John, 2009.
Znajdź pełny tekst źródłaWiley, Richard H. Chemistry of Heterocyclic Compounds, Pyrazoles and Reduced and Condensed Pyrazoles. Wiley & Sons, Incorporated, John, 2008.
Znajdź pełny tekst źródła100 years of pyrazolone drugs: An update. Basel: Birkhäuser, 1986.
Znajdź pełny tekst źródłaAktoudianakis, Evangelos. Synthesis of annulated pyrazoles via a tandem alkylation/direct arylation sequence. 2006.
Znajdź pełny tekst źródłaCzęści książek na temat "Pyrazoles"
Rauf, Abdul, i Nida Nayyar Farshori. "Pyrazoles". W SpringerBriefs in Molecular Science, 39–46. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_6.
Pełny tekst źródłaBrown, E. G. "Pyrazoles". W Ring Nitrogen and Key Biomolecules, 60–67. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4906-8_3.
Pełny tekst źródłaLi, Jie Jack, i Minmin Yang. "Pyrazoles". W Drug Discovery with Privileged Building Blocks, 173–85. Boca Raton: CRC Press, 2021. http://dx.doi.org/10.1201/9781003190806-21.
Pełny tekst źródłaAkhmetova, Vnira R., Nail S. Akhmadiev i Askhat G. Ibragimov. "Sulfur-Containing Pyrazoles, Pyrazolines and Indazoles". W N-Heterocycles, 275–312. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_7.
Pełny tekst źródłaGandhi, Divyani, Ayushi Sethiya, Nusrat Sahiba, Dinesh Kumar Jangid i Shikha Agarwal. "Nanocatalysed Synthesis of Pyrazoles, Indazoles, and Pyrazolines". W Nanocatalysis, 219–43. New York: CRC Press, 2022. http://dx.doi.org/10.1201/9781003141488-10.
Pełny tekst źródłaFustero, Santos, Antonio Simón-Fuentes, Oscar Delgado i Raquel Román. "Fluorinated Pyrazoles and Indazoles". W Fluorine in Heterocyclic Chemistry Volume 1, 279–321. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04346-3_7.
Pełny tekst źródłaGupta, Shyam L., Surendra Saini, Pratibha Saini, Anshu Dandia, K. L. Ameta i Vijay Parewa. "Pyrazoles, Indazoles and Pyrazolines: Recent Developments and Their Properties". W N-Heterocycles, 415–41. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_12.
Pełny tekst źródłaRoy, Sudipta, Sujata Roy i Gordon W. Gribble. "Metalation of Pyrazoles and Indazoles". W Topics in Heterocyclic Chemistry, 155–260. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/7081_2012_82.
Pełny tekst źródłaElguero, José, Artur M. S. Silva i Augusto C. Tomé. "Five-Membered Heterocycles: 1,2-Azoles. Part 1. Pyrazoles". W Modern Heterocyclic Chemistry, 635–725. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527637737.ch8.
Pełny tekst źródłaHamper, Bruce C., Kindrick L. Leschinsky, Deborah A. Mischke i S. Douglas Prosch. "Chiral 3-Aryl-4-halo-5-(trifluoromethyl)pyrazoles". W ACS Symposium Series, 272–81. Washington, DC: American Chemical Society, 1999. http://dx.doi.org/10.1021/bk-2000-0746.ch019.
Pełny tekst źródłaStreszczenia konferencji na temat "Pyrazoles"
Zanatta, Nilo, Marcio M. Lobo, Bruna Canova, Helio G. Bonacorso i Marcos A. P. Martins. "Regioselective synthesis of 1,3- and 1,5-substituted pyrazoles and pyrazolynes analogous of Celecoxib". W 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20138818469.
Pełny tekst źródłaMedjahed, Nassima, Zahira Kibou, Amina Berrichi, Redouane Bachir i Noureddine Choukchou-Braham. "Nickel-Catalyzed, One-Pot Synthesis of Pyrazoles". W International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13687.
Pełny tekst źródłaKoos, M., B. Steiner i J. Gajdos. "Synthesis of Some Sulfur Bridged Pyrimidines, Pyrazoles and Imidazoles". W The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02002.
Pełny tekst źródłaOumessaoud, Asmaa, Jamila Bouali, Salha Hamri, Hajiba Ouchetto, Abderrafia Hafid, Mostafa Khouili i Maria Dolors Pujol. "Efficient Synthesis of New Pyrazoles Derivatives via Functionalized Aryl-Sydnones". W 1st International Electronic Conference on Catalysis Sciences. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/eccs2020-07565.
Pełny tekst źródłaТрофимов, Б., B. Trofimov, Н. Гусарова i N. Gusarova. "The development of original methodologies of directed synthesis of le-Carbs their analogs and precursors base donacetylene and its derivatives". W Topical issues of translational medicine: a collection of articles dedicated to the 5th anniversary of the day The creation of a department for biomedical research and technology of the Irkutsk Scientific Center Siberian Branch of RAS. Москва: INFRA-M Academic Publishing LLC., 2017. http://dx.doi.org/10.12737/conferencearticle_58be81ec92d17.
Pełny tekst źródłaYamini, G., M. Madhu Sekhar, G. Sravya, T. Sreenivasulu, A. Padmaja i Grigory V. Zyryanov. "Green approach for the synthesis of some new diamidomethane linked pyridinyl pyrazoles". W PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087400.
Pełny tekst źródłaRocha, Sónia, Eduarda Fernandes, Marisa Freitas, Daniela Ribeiro, Vera Silva, Pedro Gomes, Artur Silva, Alberto Araújo i M. Luísa Corvo. "Insight into the protein tyrosine phosphatase 1B (PTP1B) inhibitory activity of pyrazoles". W 6th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07490.
Pełny tekst źródłaRamteke, Avinash A. "Study the adiabatic compressibility and acoustic impedance of chlorosubstituted pyrazoles in various solvent water mixtures". W ADVANCES IN BASIC SCIENCE (ICABS 2019). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5122382.
Pełny tekst źródłaKhatri, Taslimahemad Talab, Aadil Khursheed i Pushpendra Kumar. "Water mediated synthesis of pyrano[2, 3-c]pyrazoles using L-histidine as an effective catalyst". W RECENT ADVANCES IN FUNDAMENTAL AND APPLIED SCIENCES: RAFAS2016. Author(s), 2017. http://dx.doi.org/10.1063/1.4990359.
Pełny tekst źródłaGalarraga, Elier, Neudo Urdaneta i Julio Herrera. "In vitro Anti-leishmanial and Anti-trypanosomal Activity of Hydrazones, Pyrazoles, Pyrazolo[1,5-a]pyrimidines and Pyrazolo[3,4-b]pyridines Synthesized from 6-Substituted-3-formylchromones". W 2nd International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecmc-2-a003.
Pełny tekst źródłaRaporty organizacyjne na temat "Pyrazoles"
Habben, C., L. Komorowski, W. Maringgele, A. Meller i K. Niedenzu. Reactions of Some Boron Heterocycles with Pyrazole. Fort Belvoir, VA: Defense Technical Information Center, marzec 1989. http://dx.doi.org/10.21236/ada205979.
Pełny tekst źródłaTheopold, K. H. [Oxidation catalysis with tris(pyrazolyl)borate metal complexes]. Office of Scientific and Technical Information (OSTI), styczeń 1993. http://dx.doi.org/10.2172/6487292.
Pełny tekst źródłaTheopold, K. H. [Oxidation catalysis with tris(pyrazolyl)borate metal complexes]. Progress report. Office of Scientific and Technical Information (OSTI), lipiec 1993. http://dx.doi.org/10.2172/10161252.
Pełny tekst źródłaNiedenzu, K., H. Noeth, J. Serwatowska i J. Serwatowski. Diorganyltin(IV) Di-poly(1-pyrazolyl)boarates and Related Species. Fort Belvoir, VA: Defense Technical Information Center, czerwiec 1991. http://dx.doi.org/10.21236/ada236442.
Pełny tekst źródłaSchmidt, R. D., G. S. Lee, P. F. Pagoria, A. R. Mitchell i 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), maj 2001. http://dx.doi.org/10.2172/15005359.
Pełny tekst źródłaWilson, Bobby L. The Study of Some Early Transition Metals in Oxidation State IV Using the Potassium Poly(pyrazolyl)borates as Ligands. Fort Belvoir, VA: Defense Technical Information Center, październik 1985. http://dx.doi.org/10.21236/ada164074.
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