Literatura académica sobre el tema "TRIAZOLO-PYRIMIDINE"
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Artículos de revistas sobre el tema "TRIAZOLO-PYRIMIDINE"
Jakubowski, Mateusz, Iwona Łakomska, Adriana Kaszuba, Andrzej Wojtczak, Jerzy Sitkowski y Andrzej A. Jarzęcki. "Factors Affecting the Stability of Platinum(II) Complexes with 1,2,4-Triazolo[1,5-a]pyrimidine Derivatives and Tetrahydrothiophene-1-Oxide or Diphenyl Sulfoxide". International Journal of Molecular Sciences 23, n.º 7 (26 de marzo de 2022): 3656. http://dx.doi.org/10.3390/ijms23073656.
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 completoBadolato, Mariateresa, Fabrizio Manetti, Antonio Garofalo y Francesca Aiello. "Triazolopyrimidinium salts: discovery of a new class of agents for cancer therapy". Future Medicinal Chemistry 12, n.º 5 (marzo de 2020): 387–402. http://dx.doi.org/10.4155/fmc-2019-0317.
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 completoArgăseală, Aura, Cătălin Maxim, Mihaela Badea, Larisa Ioniță, Mariana Carmen Chifiriuc, Arpad Mihai Rostas, Mihaela Bacalum et al. "Insights into Structure and Biological Activity of Copper(II) and Zinc(II) Complexes with Triazolopyrimidine Ligands". Molecules 27, n.º 3 (24 de enero de 2022): 765. http://dx.doi.org/10.3390/molecules27030765.
Texto completoNassar, Ibrahim F., Mohammed T. Abdel Aal, Wael A. El-Sayed, Mahmoud A. E Shahin, Elsayed G. E. Elsakka, Mahmoud Mohamed Mokhtar, Maghawry Hegazy, Mohamed Hagras, Asmaa A. Mandour y Nasser S. M. Ismail. "Discovery of pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives as novel CDK2 inhibitors: synthesis, biological and molecular modeling investigations". RSC Advances 12, n.º 23 (2022): 14865–82. http://dx.doi.org/10.1039/d2ra01968j.
Texto completoFan, Ning-Juan, Yuan-feng Li, Shuang Liang y Jiang-Jiang Tang. "Synthesis and cytotoxic activity of novel steroidal derivatives containing a [1,2,4]triazolo[1,5-a]pyrimidine ring". Journal of Chemical Research 41, n.º 7 (julio de 2017): 413–15. http://dx.doi.org/10.3184/174751917x14967701767003.
Texto completoŁakomska, Iwona, Dariusz Śmiłowicz, Mateusz Jakubowski, Jerzy Sitkowski y Andrzej Wojtczak. "Platinum(II) Complexes with Bulky Disubstitute Triazolopyrimidines as Promising Materials for Anticancer Agents". Materials 13, n.º 23 (24 de noviembre de 2020): 5312. http://dx.doi.org/10.3390/ma13235312.
Texto completoHossain, M. I. y M. M. H. Bhuiyan. "Synthesis and Antimicrobial Activities of Some New Thieno and Furopyrimidine Derivatives". Journal of Scientific Research 1, n.º 2 (23 de abril de 2009): 317–25. http://dx.doi.org/10.3329/jsr.v1i2.2299.
Texto completoTang, Caifei, Zhiming Li y Quanrui Wang. "IBD-mediated oxidative cyclization of pyrimidinylhydrazones and concurrent Dimroth rearrangement: Synthesis of [1,2,4]triazolo[1,5-c]pyrimidine derivatives". Beilstein Journal of Organic Chemistry 9 (25 de noviembre de 2013): 2629–34. http://dx.doi.org/10.3762/bjoc.9.298.
Texto completoTesis sobre el tema "TRIAZOLO-PYRIMIDINE"
Xu, Kuiying. "Pyrrolo[2,3-d]pyrimidine, Pyrazolo[3,4-d]pyrimidine and Triazolo[4,5-d]pyrimidine nucleosides and oligonucleotides: Synthesis, physical properties and base-pairing = Pyrrolo[2,3-d]pyrimidin, Pyrazolo[3,4-d]pyrimidin und Triazolo[4,5-d]pyrimidin nucleoside und oligonucleotide: Synthese, physikalische Eigenschaften und Basenpaarung /". Osnabrück, 2008. http://opac.nebis.ch/cgi-bin/showAbstract.pl?sys=000254557.
Texto completoCapítulos de libros sobre el tema "TRIAZOLO-PYRIMIDINE"
Kleschick, William A., Mark J. Costales, B. Clifford Gerwick, J. B. Holtwick, R. W. Meikle, W. T. Monte, N. R. Pearson et al. "1,2,4-Triazolo[1,5-a]pyrimidine-2-sulfonanilide Herbicides". En Synthesis and Chemistry of Agrochemicals III, 10–16. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch002.
Texto completoKleschick, William A., C. M. Carson, Mark J. Costales, J. J. Doney, B. Clifford Gerwick, J. B. Holtwick, R. W. Meikle et al. "1,2,4-Triazolo[1,5-a]pyrimidine-2-sulfonanilide Herbicides". En Synthesis and Chemistry of Agrochemicals III, 17–25. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch003.
Texto completoCostales, Mark J., William A. Kleschick y B. Clifford Gerwick. "N-(Substituted-2-fluorophenyl)- andN-(Substituted-2-trifluoromethylphenyl)-1,2,4-triazolo-[1,5-a]pyrimidine-2-sulfonanilides". En Synthesis and Chemistry of Agrochemicals III, 26–33. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch004.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of bromine-bridged copper(II) dimer with 5,7-dimethyl[1,2,4-triazolo(1,5-α)]pyrimidine". En Magnetic Properties of Paramagnetic Compounds, 932–33. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_532.
Texto completoPardasani, R. T. y P. Pardasani. "Magnetic properties of trans-aquatrichlorobis-(5, 7-dimethyl[1, 2, 4]triazolo[1, 5-a]pyrimidine-N3)-ruthenium(III) monohydrate". En Magnetic Properties of Paramagnetic Compounds, 447–48. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_231.
Texto completo"Kap. 2: Azapurine, Formamid als „Wunderreagenz“, Purinsynthese und Dimethylformamid/DimethylsulfatKomplexe". En Von Aromaten und Heterocyclen zur Bio- und Nanotechnologie, 39–52. GNT-Verlag GmbH, 2023. http://dx.doi.org/10.47261/1551-2.
Texto completoFischer, Gunther. "Recent Progress in 1,2,4-Triazolo[1,5-a]pyrimidine Chemistry". En Advances in Heterocyclic Chemistry, 143–219. Elsevier, 2007. http://dx.doi.org/10.1016/s0065-2725(07)95003-5.
Texto completoFischer, Gunther. "Recent advances in 1,2,4-triazolo[1,5-a]pyrimidine chemistry". En Advances in Heterocyclic Chemistry, 1–101. Elsevier, 2019. http://dx.doi.org/10.1016/bs.aihch.2018.10.002.
Texto completoLauria, Antonino, Chiara Patella, Patrizia Diana, Paola Barraja, Alessandra Montalbano, Gaetano Dattolo, Girolamo Cirrincione y Anna Maria Almerico. "New Tetracyclic Ring System of Biological Interest Indolo[3,2-e][1,2,3]triazolo[1,5-a]pyrimidine through domino reactions of 2-azidoindole". En 19th International Congress on Heterocyclic Chemistry, 224. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50216-1.
Texto completoActas de conferencias sobre el tema "TRIAZOLO-PYRIMIDINE"
Scapin, Elisandra, Lilian Buriol, Taiana Scalco München, Clarissa Piccinin Frizzo y Marcos A. P. Martins. "Synthesis of 1,2,4-Triazolo[1,5-a]pyrimidine Supported under Ultrasound Irradiation". En 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20131012143813.
Texto completoScapin, Elisandra, Lilian Buriol, Taiana Scalco München, Clarissa Piccinin Frizzo, Mara Marzari y Marcos A. P. Martins. "Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods". En 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0028-1.
Texto completoLyapustin, D. N., E. N. Ulomsky, E. K. Voinkov y V. L. Rusinov. "Preparation of new 5-methylthio-6-nitro-1,2,4-triazolo[1,5-a]pyrimidine-7-ones as structural analogues of antiviral drugs". En PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087320.
Texto completoGharib, Ali, Mina Roshani y Manouchehr Jahangir. "Efficient Catalytic Synthesis of Pyrazolo[3,4-d]pyrimidine, Pyrazolo[4,3- e][1,2,4]triazolo[1,5-c]pyrimidine, Pyrazolo[4,3-e][1,2,4]triazolo[1,5- c]pyrimidine, Pyrazolo[3,4-d]pyrimidin-4-one derivatives using Heterogeneous Preyssler Heteropolyacid, H14[NaP5W30O110]/SiO2". En The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00169.
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