Artículos de revistas sobre el tema "Triazale"
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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 completoJansa, Petr, Petr Špaček, Ivan Votruba, Petra Břehová, Martin Dračínský, Blanka Klepetářová y Zlatko Janeba. "Efficient one-pot synthesis of polysubstituted 6-[(1H-1,2,3-triazol-1-yl)methyl]uracils through the “click” protocol". Collection of Czechoslovak Chemical Communications 76, n.º 9 (2011): 1121–31. http://dx.doi.org/10.1135/cccc2011074.
Texto completoRajeswar Rao, Vedula, Vedula M. Sharma y Tadepally V. Padmanabha Rao. "Synthesis of Some New Type of Naphthothiazole Triazoles from Lawsone". Collection of Czechoslovak Chemical Communications 58, n.º 5 (1993): 1191–94. http://dx.doi.org/10.1135/cccc19931191.
Texto completoHajri, A., D. Alimi, K. Rtibi y H. Sebai. "Novel 6-aryl-7-alkyl/aryl-[1,2,4]triazolo[4,3-a][1,3,5]triazine-5(6H)-thiones, processes for their preparation, characterization and evaluation of their in vitro antioxidant activity". Bulletin of the Chemical Society of Ethiopia 35, n.º 3 (31 de enero de 2022): 565–72. http://dx.doi.org/10.4314/bcse.v35i3.8.
Texto completoSlivka, Mikhailo, Nataliya Korol, Ivan Rusyn y Vasyl Lendel. "Synthesis of [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium and [1,2,4]triazolo[5,1-b][1,3]thiazin-4-ium salts via regioselective electrophilic cyclization of 3-[(2-alken-1-yl)sulfanyl]-4H-1,2,4-triazoles". Heterocyclic Communications 21, n.º 6 (1 de diciembre de 2015): 397–401. http://dx.doi.org/10.1515/hc-2015-0158.
Texto completoCaiana, Rodrigo Ribeiro Alves, Cosme Silva Santos, Ronaldo Nascimento de Oliveira y Juliano Carlo Rufino Freitas. "Scientific and Technological Prospecting of 1H-1,2,3-Triazoles". Current Organic Chemistry 26, n.º 3 (febrero de 2022): 275–86. http://dx.doi.org/10.2174/1385272826666220126153429.
Texto completoPandey, Vinod Kumar, Zehra Tusi, Sumerah Tusi y Madhawanand Joshi. "Synthesis and Biological Evaluation of Some Novel 5-[(3-Aralkyl Amido/Imidoalkyl) Phenyl]-1,2,4-Triazolo[3,4-b]-1,3,4-Thiadiazines as Antiviral Agents". ISRN Organic Chemistry 2012 (11 de septiembre de 2012): 1–7. http://dx.doi.org/10.5402/2012/760517.
Texto completoRyzhikova, Olga V., Kseniya N. Sedenkova, Sergey V. Kositov, Victor A. Tafeenko, Yuri K. Grishin y Elena B. Averina. "Stereoselective Approach to Hydroxyalkyl-1,2,3-triazoles Containing Cyclooctane Core and Their Use for CuAAC Catalysis". Catalysts 13, n.º 5 (3 de mayo de 2023): 835. http://dx.doi.org/10.3390/catal13050835.
Texto completoOhloblina, M. V. "Biological features of new 1,2,4-triazole derivatives (a literature review)". Current issues in pharmacy and medicine: science and practice 15, n.º 1 (15 de febrero de 2022): 107–12. http://dx.doi.org/10.14739/2409-2932.2022.1.252305.
Texto completoFedotov, S. O. y A. S. Hotsulia. "Synthesis and properties of 3-(ethylthio)-9-methyl-6-(alkylthio)pyrazolo[1,5-d][1,2,4]triazolo[3,4-f][1,2,4]triazines". Current issues in pharmacy and medicine: science and practice 15, n.º 3 (15 de noviembre de 2022): 227–34. http://dx.doi.org/10.14739/2409-2932.2022.3.263994.
Texto completoRathmann, Stephanie M., Nancy Janzen y John F. Valliant. "Synthesis, radiolabelling, and biodistribution studies of triazole derivatives for targeting melanoma". Canadian Journal of Chemistry 94, n.º 9 (septiembre de 2016): 773–80. http://dx.doi.org/10.1139/cjc-2016-0239.
Texto completoGotsulya, A. S., A. I. Panasenko, E. G. Knysh y A. O. Pryimenko. "UV-spectrophotometric study of the 7-((3-thio-4-R-1,2,4-triazole-3-yl)methyl)-theophyllines". Farmatsevtychnyi zhurnal, n.º 4 (4 de septiembre de 2018): 65–70. http://dx.doi.org/10.32352/0367-3057.4.15.03.
Texto completoSonawane, R. y M. A. Sagare. "Design, Synthesis and Evaluation of Some Substituted Triazole Phenyl Methanones from Substituted Anilines". Asian Journal of Organic & Medicinal Chemistry 7, n.º 4 (2023): 295–98. http://dx.doi.org/10.14233/ajomc.2022.ajomc-p405.
Texto completoBortolot, Carolina S., Luana da S.M. Forezi, Roberta K. F. Marra, Marcelo I. P. Reis, Bárbara V. F. e. Sá, Ricardo I. Filho, Zeinab Ghasemishahrestani et al. "Design, Synthesis and Biological Evaluation of 1H-1,2,3-Triazole-Linked-1H-Dibenzo[b,h]xanthenes as Inductors of ROS-Mediated Apoptosis in the Breast Cancer Cell Line MCF-7". Medicinal Chemistry 15, n.º 2 (12 de febrero de 2019): 119–29. http://dx.doi.org/10.2174/1573406414666180524071409.
Texto completoJoshi, K. A., J. M. Dhalani, H. B. Bhatt y K. M. Kapadiya. "Synthesis of some new 6-aryl-3-(4-isopropylphenyl)[1,2,4]triazolo[3,4-b][1,3,4] thiadiazoles and its anti-microbial study". Current Chemistry Letters 10, n.º 4 (2021): 479–88. http://dx.doi.org/10.5267/j.ccl.2021.4.003.
Texto completoCanseco-González, Daniel, José Luis Rodríguez de la O y José Enrique Herbert-Pucheta. "Combined XRD-paramagnetic 13C NMR spectroscopy of 1,2,3-triazoles for revealing copper traces in a Huisgen click-chemistry cycloaddition. A model case". Heterocyclic Communications 25, n.º 1 (28 de noviembre de 2019): 98–106. http://dx.doi.org/10.1515/hc-2019-0018.
Texto completoKar, C. y K. Gupta. "Effect of triazole-type plant growth regulators on sunflower and safflower seed viability". Canadian Journal of Botany 69, n.º 6 (1 de junio de 1991): 1344–48. http://dx.doi.org/10.1139/b91-174.
Texto completoRavikumar, Krishnan, Balasubramanian Sridhar, Jagadeesh Babu Nanubolu, Venkatasubramanian Hariharakrishnan y Awadesh Narain Singh. "Structures of benzoxazine-fused triazoles as potential diuretic agents". Acta Crystallographica Section C Crystal Structure Communications 68, n.º 8 (13 de julio de 2012): o302—o307. http://dx.doi.org/10.1107/s0108270112029800.
Texto completoSingh, Rakesh, Harpreet Kaur y Pankaj Gupta. "1,2,3-Triazoles: Lead Molecules For Promising Drugs: A Review". Asian Journal of Chemistry 33, n.º 12 (2021): 2896–918. http://dx.doi.org/10.14233/ajchem.2021.23488.
Texto completoKantlehner, Willi, Kai Edelmann y Wolfgang Frey. "Orthoamide und Iminiumsalze, LXXXII [1]. Die Spaltung von Alkincarbonsäure-orthoamiden mit Trimethylsilylazid / Orthoamides and Iminium Salts LXXXII [1]. The Cleavage of Orthoamides of Alkynecarboxylic Acids by Trimethylsilyl Azide". Zeitschrift für Naturforschung B 67, n.º 9 (1 de septiembre de 2012): 913–20. http://dx.doi.org/10.5560/znb.2012-0124.
Texto completoJalihal, Prabhu C., Vaibhav Rajoriya y Varsha Kashaw. "DESIGN, SYNTHESIS, AND EVALUATION OF NEW DERIVATIVE OF 1,2,4-TRIAZOLES FOR ANTIMICROBIAL AND ANTI-INFLAMMATORY ACTIVITY". International Journal of Current Pharmaceutical Research 10, n.º 4 (16 de julio de 2018): 29. http://dx.doi.org/10.22159/ijcpr.2018v10i4.28455.
Texto completoTang, Yongxing, Ziwei An, Ajay Kumar Chinnam, Richard J. Staples y Jean'ne M. Shreeve. "Very thermostable energetic materials based on a fused-triazole: 3,6-diamino-1H-[1,2,4]triazolo[4,3-b][1,2,4]triazole". New Journal of Chemistry 45, n.º 1 (2021): 85–91. http://dx.doi.org/10.1039/d0nj05152g.
Texto completoKhan, Imtiaz, Shahid Hameed, Najim A. Al-Masoudi, Nabeel A. Abdul-Reda y Jim Simpson. "New triazolothiadiazole and triazolothiadiazine derivatives as kinesin Eg5 and HIV inhibitors: synthesis, QSAR and modeling studies". Zeitschrift für Naturforschung B 70, n.º 1 (1 de enero de 2015): 47–58. http://dx.doi.org/10.1515/znb-2014-0162.
Texto completoMaj, Anna, Agnieszka Kudelko y Marcin Świątkowski. "Novel Conjugated s-Tetrazine Derivatives Bearing a 4H-1,2,4-Triazole Scaffold: Synthesis and Luminescent Properties". Molecules 27, n.º 2 (11 de enero de 2022): 459. http://dx.doi.org/10.3390/molecules27020459.
Texto completoCebeci, Yıldız Uygun y Şengül Alpay Karaoğlu. "Design and microwave-assisted synthesis of a novel Mannich base and conazole derivatives and their biological assessment". Heterocyclic Communications 27, n.º 1 (1 de enero de 2021): 100–111. http://dx.doi.org/10.1515/hc-2020-0126.
Texto completoPalchak, Zachary L., Paula T. Nguyen y Catharine H. Larsen. "Synthesis of alpha-tetrasubstituted triazoles by copper-catalyzed silyl deprotection/azide cycloaddition". Beilstein Journal of Organic Chemistry 11 (14 de agosto de 2015): 1425–33. http://dx.doi.org/10.3762/bjoc.11.154.
Texto completoБакумовська, Х. Д. y А. С. Гоцуля. "Synthesis and properties of 7-((6-aryl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazol-3-yl)methyl)theophyllines". Farmatsevtychnyi zhurnal, n.º 1 (27 de febrero de 2023): 58–65. http://dx.doi.org/10.32352/0367-3057.1.23.06.
Texto completoShah, Tariq A., Zubair Ahmad, Niyaz A. Mir, M. Muneer, Nigam P. Rath y Musheer Ahmad. "One step synthesis of highly functionalized thiazolo[3,2-b][1,2,4]triazole, triazolo[1,5-a]pyrimidine and triazolo[3,4-b][1,3,4]thiadiazine". RSC Advances 5, n.º 130 (2015): 107931–37. http://dx.doi.org/10.1039/c5ra21270g.
Texto completoCools, H. J., B. A. Fraaije, S. H. Kim y J. A. Lucas. "Impact of changes in the target P450 CYP51 enzyme associated with altered triazole-sensitivity in fungal pathogens of cereal crops". Biochemical Society Transactions 34, n.º 6 (25 de octubre de 2006): 1219–22. http://dx.doi.org/10.1042/bst0341219.
Texto completoDanilkina, Natalia A., Nina S. Bukhtiiarova, Anastasia I. Govdi, Anna A. Vasileva, Andrey M. Rumyantsev, Artemii A. Volkov, Nikita I. Sharaev et al. "Synthesis and Properties of 6-Aryl-4-azidocinnolines and 6-Aryl-4-(1,2,3-1H-triazol-1-yl)cinnolines". Molecules 24, n.º 13 (27 de junio de 2019): 2386. http://dx.doi.org/10.3390/molecules24132386.
Texto completoNeelgundmath, Mahabaleshwaraiah y Oblennavar Kotresh. "Synthesis, Evaluation and Characterization of Some 1,3,4-Triazole-2-one Derivatives as Antimicrobial Agents". E-Journal of Chemistry 9, n.º 4 (2012): 2407–14. http://dx.doi.org/10.1155/2012/672125.
Texto completoAli, Abdelselam S., John S. Wilkie y Kevin N. Winzenberg. "Synthesis of Some 1H-1,2,4-Triazole, 4H-1,2,4-Triazole, Thiazolo[2,3-c]-1,2,4-triazole and 5H-1,2,4-Triazolo-[3,4-b][1,3]thiazine Derivatives by Metal Compound-Mediated Oxidative Cyclization of Derivatives of 2-(Phenylmethylidene)hydrazinecarboximidothioic Acid". Australian Journal of Chemistry 50, n.º 9 (1997): 911. http://dx.doi.org/10.1071/c97058.
Texto completoMroczyńska, Martyna, Ewelina Kurzyk, Magdalena Śliwka-Kaszyńska, Urszula Nawrot, Marta Adamik y Anna Brillowska-Dąbrowska. "The Effect of Posaconazole, Itraconazole and Voriconazole in the Culture Medium on Aspergillus fumigatus Triazole Resistance". Microorganisms 8, n.º 2 (19 de febrero de 2020): 285. http://dx.doi.org/10.3390/microorganisms8020285.
Texto completoSafonov, A. A. y O. I. Panasenko. "Synthesis, antimicrobial and antifungal activity of 3-(2-bromophenyl)-5-(alkylthio)-4-phenyl-4H-1,2,4-triazoles". Current issues in pharmacy and medicine: science and practice 15, n.º 3 (15 de noviembre de 2022): 235–40. http://dx.doi.org/10.14739/2409-2932.2022.3.264691.
Texto completoShah, Tariq A., Zubair Ahmad, Niyaz A. Mir, M. Muneer, Nigam P. Rath y Musheer Ahmad. "Correction: One step synthesis of highly functionalized thiazolo[3,2-b][1,2,4]triazole, triazolo[1,5-a]pyrimidine and triazolo[3,4-b][1,3,4]thiadiazine". RSC Advances 6, n.º 12 (2016): 9437. http://dx.doi.org/10.1039/c6ra90004f.
Texto completoTsyrenova, Biligma y Valentine Nenajdenko. "Synthesis and Spectral Study of a New Family of 2,5-Diaryltriazoles Having Restricted Rotation of the 5-Aryl Substituent". Molecules 25, n.º 3 (23 de enero de 2020): 480. http://dx.doi.org/10.3390/molecules25030480.
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 completoGümüş, Mustafa Kemal. "Green Formation of Novel Pyridinyltriazole-Salicylidene Schiff Bases". Current Organic Synthesis 16, n.º 2 (26 de marzo de 2019): 309–13. http://dx.doi.org/10.2174/1570179416666181207145951.
Texto completoAguiar, Renata Alves, Marcos Gomes Cunha, Fernando Godinho Araújo, Luciana Celeste Carneiro, Edson Pereira Borges y Valtemir José Carlin. "EFFICIENCY LOSS OF RECORDED FUNGICIDES FOR THE CONTROL OF ASIAN SOYBEAN RUST IN CENTRAL REGION OF BRAZIL". JOURNAL OF NEOTROPICAL AGRICULTURE 3, n.º 2 (2 de septiembre de 2016): 41–47. http://dx.doi.org/10.32404/rean.v3i2.1066.
Texto completoRai, Vishakha, Kavyashree P., Sarvesh S. Harmalkar, Sundar N. Dhuri y Mahagundappa R. Maddani. "1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N1 and N2 substituted triazoles". Organic & Biomolecular Chemistry 20, n.º 2 (2022): 345–51. http://dx.doi.org/10.1039/d1ob01717a.
Texto completoGovdi, Anastasia I., Polina V. Tokareva, Andrey M. Rumyantsev, Maxim S. Panov, Johannes Stellmacher, Ulrike Alexiev, Natalia A. Danilkina y Irina A. Balova. "4,5-Bis(arylethynyl)-1,2,3-triazoles—A New Class of Fluorescent Labels: Synthesis and Applications". Molecules 27, n.º 10 (17 de mayo de 2022): 3191. http://dx.doi.org/10.3390/molecules27103191.
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