Literatura académica sobre el tema "Triazale"
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Artículos de revistas sobre el tema "Triazale"
Syrota, Natalia O., Sergiy V. Kemskiy, Lesya M. Saliyeva y Mykhailo V. Vovk. "1,2,3-Triazole-4(5)-amines – Convenient Synthetic Blocks for the Construction of Triazolo-Annulated Heterocycles". Journal of Organic and Pharmaceutical Chemistry 20, n.º 2 (20 de julio de 2022): 27–51. http://dx.doi.org/10.24959/ophcj.22.258512.
Texto completoPathak, Suraj Kumar, Yepeng Xiang, Manli Huang, Taian Huang, Xiaosong Cao, He Liu, Guohua Xie y Chuluo Yang. "Fused tetracyclic tris[1,2,4]triazolo[1,3,5]triazine as a novel rigid electron acceptor for efficient thermally activated delayed fluorescence emitters". RSC Advances 10, n.º 26 (2020): 15523–29. http://dx.doi.org/10.1039/d0ra01925a.
Texto completoZeng, Qun, Yanyang Qu, Jinshan Li y Hui Huang. "Theoretical studies on the derivatives of tris([1,2,4]triazolo)[4,3-a:4′,3′-c:4′′,3′′-e][1,3,5]triazine as high energetic compounds". RSC Advances 6, n.º 7 (2016): 5419–27. http://dx.doi.org/10.1039/c5ra22524h.
Texto completoHryhorka, H. V., М. М. Fizer, О. І. Fizer, A. O. Kryvoviaz y M. V. Slivka. "SYNTHESIS AND CHEMICAL PROPERTIES OF 2-HEPTADECYL-[1,3]THIAZOLO[3,2-b][1,2,4]TRIAZOL-7-IUM CATION". Scientific Bulletin of the Uzhhorod University. Series «Chemistry» 48, n.º 2 (23 de mayo de 2023): 67–72. http://dx.doi.org/10.24144/2414-0260.2022.2.67-72.
Texto completoFranco, Daiana Portella, Lucas Caruso, Nathalia Fonseca Nadur, Thiago Moreira Pereira, Renata Barbosa Lacerda y Arthur Eugen Kümmerle. "Recent Advances in Microwave-Assisted Synthesis and Functionalization of 1,2,3- and 1,2,4-triazoles". Current Organic Chemistry 25, n.º 23 (16 de diciembre de 2021): 2815–39. http://dx.doi.org/10.2174/1385272825666211011111408.
Texto completoWang, Jiazhuang, Jianhua Yang, Xuxin Fu, Guiping Qin, Tiebo Xiao y Yubo Jiang. "Synthesis of Triazole-Fused Phenanthridines through Pd-Catalyzed Intramolecular Phenyl C–H Activation of 1,5-Diaryl-1,2,3-triazoles". Synlett 30, n.º 12 (19 de junio de 2019): 1452–56. http://dx.doi.org/10.1055/s-0037-1611859.
Texto completoKarpun, Yevhen y Nataliia Polishchuk. "Synthesis and antimicrobial activity of s-substituted derivatives of 1,2,4-triazol-3-thiol". ScienceRise: Pharmaceutical Science, n.º 3(31) (30 de junio de 2021): 64–69. http://dx.doi.org/10.15587/2519-4852.2021.235976.
Texto completoFizer, O. I., M. M. Fizer, A. O. Kryvoviaz y M. V. Slivka. "INVESTIGATION OF THE INFLUENCE OF THE SUBSTITUTE IN THE THIRD POSITION ON THE ELECTRONIC STRUCTURE OF 1,3-THIAZOLO[2,3-c][1,2,4]TRIAZOLE". Scientific Bulletin of the Uzhhorod University. Series «Chemistry» 46, n.º 2 (10 de febrero de 2022): 55–62. http://dx.doi.org/10.24144/2414-0260.2021.2.55-62.
Texto completoKhomenko, Dmytro, Tetyana Shokol, Roman Doroshchuk, Ilona Raspertova, Rostyslav Lampeka y Yulian Volovenko. "Strategies for the Synthesis of [1,2,4]Triazolo[1,5-a]pyridine-8-carbonitriles". Chemistry & Chemical Technology 17, n.º 2 (1 de junio de 2023): 294–303. http://dx.doi.org/10.23939/chcht17.02.294.
Texto completoFarrán, M. Ángeles, M. Ángels Bonet, Rosa M. Claramunt, M. Carmen Torralba, Ibon Alkorta y José Elguero. "The structures of 1,4-diaryl-5-trifluoromethyl-1H-1,2,3-triazoles related to J147, a drug for treating Alzheimer's disease". Acta Crystallographica Section C Structural Chemistry 74, n.º 4 (28 de marzo de 2018): 513–22. http://dx.doi.org/10.1107/s2053229618004394.
Texto completoTesis sobre el tema "Triazale"
Horner, Katherine A. "Synthesis and applications of triazole- and triazine-containing amino acids". Thesis, University of Leeds, 2015. http://etheses.whiterose.ac.uk/11024/.
Texto completoVieira, Andreia Sofia da Costa. "Rethinking Triazoles as Antifungals: Synthesis and Evaluation of New Triazole Derivatives". Master's thesis, Universidade Nova de Lisboa, Instituto de Tecnologia Química e Biológica António Xavier, 2017. http://hdl.handle.net/10362/81407.
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Khaldi, Zineb. "Elaboration et évaluation biologique de nouveaux matériaux lignocellulosiques antibactériens". Thesis, Limoges, 2018. http://www.theses.fr/2018LIMO0090/document.
Texto completoThe contamination of surfaces by bacteria and the emergence of antimicrobial resistant strains are very worrying problems in different areas such as hospital and food. This contamination begins with the adhesion of pathogenic bacteria on a surface until the formation of biofilms. These biofilms contribute to the emergence of resistances of certain bacterial strains to conventional treatments. To answer these problems of surface contamination, this thesis work focuses on the development of new antibacterial materials based on pulp fibers. In the first part, we focused on the development of an antibacterial paper by grafting, via triazine link, two essential oil compounds, thymol and carvacrol, known for their antibacterial activities. The microbiological evaluation of the developed materials against the two bacterial strains tested, E. coli and S. aureus, showed a bacteriostatic effect. These materials block the bacterial growth thus preventing the biofilms formation. Synergy between thymol and carvacrol grafted onto paper has also been shown. In a second part, our study focused on the development of an antibacterial paper that acquires its activity only after the grafting and formation of "aryl-1,2,3-triazole", the active motif. The grafting is carried out by a reaction of "Click Chemistry", the copper (I)-catalyzed Azide Alkyne Cycloaddition. The antibacterial tests reveal the importance of the aryl substituent, the influence of the contact time and the relevance of using mixtures of materials. The antibacterial activity observed on the thermomechanical pulp fibers is better in both parts. The different results obtained are described in this manuscript
Fiscus, David Michael. "The chemistry of 3-diazo-3H̲-1,4-triazole and 3H̲-1,2,4- triazol-3-ylidene /". The Ohio State University, 1985. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487260135358319.
Texto completoCanduzini, Hugo Antonio. "Síntese e funcionalização de 1,2,3-triazóis via reação de cicloadição [3+2] de azidas e acetilenos terminais". Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/9/9138/tde-07032013-094439/.
Texto completoThe aim of this work has been exploring the synthesis and functionalization of 1,2,3-triazoles employing the use of \"click-chemistry\" concept, which is defined as an approach for synthesis of various compounds based on reactions of carbon-heteroatom bond formation, which the reaction is stereospecific, high-efficiently, commonly gives high yields and in some cases no by-products are formed. The compound 1,2,3-triazole, which is the main starting material for the next steps was prepared from propargyl alcohol (4) in the presence of an organic azide (1) and copper(I) as a reaction promoter. Subsequently with a series of 1,2,3-triazole (2n) prepared we proceeded to the next step which is the substitution of hydroxyl for a tosyl group and after that a multicomponent cycloaddition of a new 1,2,3-triazole compound forming bis-triazoles. Bis-triazoles (5) were tested against fungal strains, responsible for dermatitis, with delighted results, furhtermore this class of strutures can be used as building blocks to improve efficiency in some other more complex structure.
Cong, Mei. "Design, synthesis and characterization of novel triazole nucleoside analogues". Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM4018.
Texto completoNucleoside mimics are of considerable importance in the search of antiviral and anticancer drug candidates. One noteworthy example is ribavirin, the first synthetic antiviral triazole nucleoside discovered 40 years ago, which is still actively in clinic use for treating hepatitis C infection and emerging viral pandemics. Recently, ribavirin has been also reported to demonstrate apoptosis-related anticancer effects and is in clinical trial for treating leukemia. Consequently, there is a renewed interest in creating new structural entities of triazole nucleosides with the aim of developing potent therapeutic agents with novel mechanisms of action. During my PhD program, I have been actively engaged in constructing structurally novel O-arylated and S-arylated triazole nucleosides. The O-arylated triazole nucleosides were obtained via microwave promoted aromatic nucleophilic substitution, whereas the S-arylated triazole nucleosides were synthesized via C-S coupling reaction using our newly developed mixed ligand Pd catalyst (Pd2(dba)3/Xantphos/CyPF-tBu). The concept of the mixed ligand catalyst system is extremely advantageous and rewarding, offering a unique opportunity to rationally combine ligands with complementary features in order to promote the reactions with challenging substrates which are otherwise difficult to proceed. Finally, in order to improve bioavailability of the active triazole nucleoside analogues identified in our group, I have attempted to conjugate the triazole nucleoside to an amphiphilic dendrimer in the view to establishing an effective drug delivery system and offering a better bioavailability
REDENTI, SARA. "DESIGN, SYNTHESIS AND CHARACTERIZATION OF GSK-3β AND CK-1δ INHIBITORS". Doctoral thesis, Università degli Studi di Trieste, 2017. http://hdl.handle.net/11368/2908172.
Texto completoWareman, P. J. "Regioselectivity of 1,2,4-triazole". Thesis, Swansea University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639348.
Texto completoObszynski, Julie. "Conception et synthèse d'aminoglycosides guidées par l'ARN". Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF018.
Texto completoThe development of new antibiotics is a major public health issue. Given the high potential of aminoglycosides as antibiotics, these compounds have aroused great interest in many research groups. However, despite their maturity, their use is still limited because of their toxicity and the increasing development of resistance mechanisms to aminoglycosides. To better understand the problems inherent to their use, it is crucial to understand their action a cellular level, and to study the interactions with their molecular targets (RNA and protein). In addition to their antibiotic power, aminoglycosides are also universal ligands for several RNAs, capable of specific interactions with RNAs of HIV-1: DIS, TAR and RRE. The elaboration of modified aminoglycosides presents a huge advantage because the domain of application, and therefore the benefits, are important. Nevertheless, the structural complexity of these molecules is a major constraint, chemoselective functionalization is essential but unfortunately poorly described in the literature.In this work, we developed two approaches to target the DIS and/or the A site of the bacterialribosome. The first one, unique but challenging is based on the concept of in situ click chemistry. The second approach is conventional and is based on the selective functionalization of some keypositions of aminoglycosides
Small, A. "Regiospecific reactions of 1,2,4-triazole". Thesis, Swansea University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.639059.
Texto completoLibros sobre el tema "Triazale"
Košmrlj, Janez, ed. Click Triazoles. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-29429-7.
Texto completoBallantine, Larry G., Janis E. McFarland y Dennis S. Hackett, eds. Triazine Herbicides: Risk Assessment. Washington, DC: American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0683.
Texto completoDehaen, Wim y Vasiliy A. Bakulev, eds. Chemistry of 1,2,3-triazoles. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-07962-2.
Texto completo1944-, Ballantine Larry Gene, McFarland Janis E. 1956- y Hackett Dennis S. 1950-, eds. Triazine herbicides: Risk assessment. Washington, DC: American Chemical Society, 1998.
Buscar texto completoSaka, John Danwell Kalenga. Studies in 1, 2, 3-triazine chemistry. Norwich: University of East Anglia, 1985.
Buscar texto completoBlackman, Claire. Studies on carbinolamine-containing triazine antitumour agents. Portsmouth: University of Portsmouth, 1994.
Buscar texto completoByrne, John Joseph. Disease Control and Yield Improvement in Winter Wheat using Strobilurin and Triazole Chemistry. Dublin: University College Dublin, 1998.
Buscar texto completoUnited States. Environmental Protection Agency. Office of Pesticide Programs. Special Review and Reregistration Division. Reregistration eligibility decision: 1,3,5-triethylhexahydro-s-triazine, list C, case 3147. [Washington, D.C.?]: Environmental Protection Agency, Office of Pesticide Programs, Special Review and Reregistration Division, 1997.
Buscar texto completoFeakin, Stephanie J. Biotreatment of surface waters to remove s-triazine herbicides: FR/K 0002, June, 1994. Marlow, Buckinghamshire: Foundation for Water Research, 1994.
Buscar texto completoD, Sobel Jack y Wayne State University. School of Medicine., eds. Clinical perspectives: Terconazole, an advance in vulvovaginal candidiasis therapy : proceedings from a symposium, Laguna Niguel, California, October 15-16, 1987. New York, NY: BMI/McGraw-Hill, 1988.
Buscar texto completoCapítulos de libros sobre el tema "Triazale"
Aizpurua, Jesus M., Maialen Sagartzazu-Aizpurua y Zaira Monasterio. "Mesoionic 1,2,3-Triazoles and 1,2,3-Triazole Carbenes". En Topics in Heterocyclic Chemistry, 211–67. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/7081_2014_120.
Texto completoCrowley, James D. y David A. McMorran. "“Click-Triazole” Coordination Chemistry: Exploiting 1,4-Disubstituted-1,2,3-Triazoles as Ligands". En Topics in Heterocyclic Chemistry, 31–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/7081_2011_67.
Texto completoRauf, Abdul y Nida Nayyar Farshori. "Triazoles". En SpringerBriefs in Molecular Science, 57–64. Dordrecht: Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_8.
Texto completoGooch, Jan W. "Triazine". En Encyclopedic Dictionary of Polymers, 762. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12076.
Texto completoGooch, Jan W. "Triazine Resin". En Encyclopedic Dictionary of Polymers, 762. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12077.
Texto completoGooch, Jan W. "Trihydrazide Triazine". En Encyclopedic Dictionary of Polymers, 766. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_12127.
Texto completoEdmunds, Andrew J. F. "Triazine Herbicides". En Bioactive Heterocyclic Compound Classes, 21–38. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664412.ch2.
Texto completoBährle-Rapp, Marina. "Ethylhexyl Triazone". En Springer Lexikon Kosmetik und Körperpflege, 193. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_3767.
Texto completoMuir, D. C. G. "Triazine Herbicides". En Mass Spectrometry in Environmental Sciences, 423–35. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2361-7_19.
Texto completoMejlsøe, S. L. y A. Kakkar. "CHAPTER 7. N-Heterocyclic Dendrimers: Hyperbranched Frameworks Containing Triazole, Triazine, Porphyrin and Phthalocyanine Ring Structures". En Monographs in Supramolecular Chemistry, 183–229. Cambridge: Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781788012904-00183.
Texto completoActas de conferencias sobre el tema "Triazale"
Tyrkov, Alexey, Svetlana Luzhnova, Evgenia Utyaganova y Ekaterina Yurtayeva. "Promising materials based on Tetrahydro-[1,2,4]Oxadiazole[3,2-C][1,4]Oxazine for innovative biotechnologies". En "The Caspian in the Digital Age" within the framework of the International Scientific Forum "Caspian 2021: Ways of Sustainable Development". Dela Press Publishing House, 2022. http://dx.doi.org/10.56199/dpcsebm.sddh5085.
Texto completoChachibaia, Tamar y Joy Hoskeri. "In silico computer simulation risk assessment of triazole fungicides on human cytochrome p450 aromatase enzyme: cyp19a1 inhibition by triazoles using autodock software." En MOL2NET, International Conference on Multidisciplinary Sciences. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/mol2net-1-f002.
Texto completoJenkins, Alyn, Santosh Gopi, Jody Hoshowski, Warinthon Lertpornsuksawat, Jennifer Jackson y Thomas Wilson. "Application of a New H2S Scavenger with Improved Performance in The Field". En SPE Annual Technical Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/206057-ms.
Texto completoSilva, Marina Goulart da, Graziele Diniz da Silva, Clebson L.Veber, Andersson Barison, Gustavo H. R. Viana y José Augusto F. P. Villar. "Design and synthesis of triazole-chalcones." En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0263-1.
Texto completoYu, Pan, Ningning Liu, Weiyuan Yuan, Yining Wen y Qinpei Wu. "Synthesis of 1,2,3- Triazole Nucleoside Analogues". En 2015 International Conference on Industrial Technology and Management Science. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/itms-15.2015.264.
Texto completoDreyer, Christian, Alfred Blume, Monika Bauer, Jörg Bauer y Jens Neumann-Rodekirch. "Triazine based Dendrimers". En The 4th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01879.
Texto completoPatel, Hasmukh, Kenneth Johnson y Roland Martinez. "Triazine Polymers for Improving Elastic Properties in Oil Well Cements". En SPE International Conference on Oilfield Chemistry. SPE, 2021. http://dx.doi.org/10.2118/204333-ms.
Texto completoRangel-Rojo, Raul, Hiro Matsuda, K. Kimura, Miguel A. Mendez-Rojas y William H. Watson. "Wavelength-resolved nonlinearity on triazole-quinone derivatives". En Optical Science and Technology, SPIE's 48th Annual Meeting, editado por Mark G. Kuzyk, Manfred Eich y Robert A. Norwood. SPIE, 2003. http://dx.doi.org/10.1117/12.502502.
Texto completoNascimento, Wilson S., Celso Amorim Camara y Ronaldo N. de Oliveira. "Synthesis of New 1,2,3-triazole-1,4-naphthoquinones". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0330-2.
Texto completoRangel-Rojo, Raul, L. Stranges, Ajoy K. Kar, M. A. Mendez-Rojas y W. H. Watson. "Near-resonance nonlinearities in triazole-quinone derivatives". En IV Iberoamerican Meeting of Optics and the VII Latin American Meeting of Optics, Lasers and Their Applications, editado por Vera L. Brudny, Silvia A. Ledesma y Mario C. Marconi. SPIE, 2001. http://dx.doi.org/10.1117/12.437064.
Texto completoInformes sobre el tema "Triazale"
Dontsova, Katerina, Susan Taylor, Jennifer Arthur, Julie Becher, Mark Brusseau, Edward Hunt, Noah Mark, Dave Ringelberg, Jirí Šimunek y Marianne Walsh. Dissolution of NTO, DNAN, and insensitive munitions formulations and their fates in soils : SERDP ER-2220. Engineer Research and Development Center (U.S.), noviembre de 2022. http://dx.doi.org/10.21079/11681/45920.
Texto completoLee, Kien-Yin y C. Storm. Preparation and properties of 3-amino-5-nitro-1,2,4-triazole. Office of Scientific and Technical Information (OSTI), octubre de 1990. http://dx.doi.org/10.2172/6870948.
Texto completoXu, Y. E. y C. S. Sung. Photophysics of Polycyanate Resin and Triazine Compounds. Fort Belvoir, VA: Defense Technical Information Center, junio de 1997. http://dx.doi.org/10.21236/ada327097.
Texto completoCaflin, Kelley C. y Peggy Sanchez. Solubility Report of 1-Methyl-3,5-Dinitro-1H-1,2,4-Triazole (MDNT) and 2-Methyl-4,5-Dinitro-2H-1,2,3-Triazole 1-Oxide (MDNTO) for Co-Crystallization Screen. Fort Belvoir, VA: Defense Technical Information Center, noviembre de 2015. http://dx.doi.org/10.21236/ada627559.
Texto completoKinkead, E. R., S. K. Bunger y R. E. Wolfe. Irritation and Sensitization Studies on Triazine T17-2. Fort Belvoir, VA: Defense Technical Information Center, enero de 1990. http://dx.doi.org/10.21236/ada221922.
Texto completoTesfaselassie, Elias. Antimalarial Drug Discovery using Triazoles to Overcome Chloroquine Resistance. Portland State University Library, enero de 2000. http://dx.doi.org/10.15760/etd.2503.
Texto completoBeal, Samuel, Matthew Bigl y Charles Ramsey. Live-fire validation of command-detonation residues testing using a 60 mm IMX-104 munition. Engineer Research and Development Center (U.S.), agosto de 2022. http://dx.doi.org/10.21079/11681/45266.
Texto completoBeal, Samuel, Matthew Bigl y Charles Ramsey. Live-fire validation of command-detonation residues testing using an 81 mm IMX-104 munition. Engineer Research and Development Center (U.S.), abril de 2023. http://dx.doi.org/10.21079/11681/46913.
Texto completoHaley, Mark V., Roman G. Kuperman y Ronald T. Checkai. Aquatic Toxicity of 3-Nitro-1,2,4-Triazol-5-One. Fort Belvoir, VA: Defense Technical Information Center, septiembre de 2009. http://dx.doi.org/10.21236/ada508035.
Texto completoStromer, Bobbi, Rebecca Crouch, Katrinka Wayne, Ashley Kimble, Jared Smith y Anthony Bednar. Methods for simultaneous determination of 29 legacy and insensitive munition (IM) constituents in aqueous, soil-sediment, and tissue matrices by high-performance liquid chromatography (HPLC). Engineer Research and Development Center (U.S.), septiembre de 2021. http://dx.doi.org/10.21079/1168142105.
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