Добірка наукової літератури з теми "TRIAZOLO-PYRIMIDINE"
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Статті в журналах з теми "TRIAZOLO-PYRIMIDINE"
Jakubowski, Mateusz, Iwona Łakomska, Adriana Kaszuba, Andrzej Wojtczak, Jerzy Sitkowski, and 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, no. 7 (March 26, 2022): 3656. http://dx.doi.org/10.3390/ijms23073656.
Повний текст джерелаShah, Tariq A., Zubair Ahmad, Niyaz A. Mir, M. Muneer, Nigam P. Rath, and 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, no. 130 (2015): 107931–37. http://dx.doi.org/10.1039/c5ra21270g.
Повний текст джерелаBadolato, Mariateresa, Fabrizio Manetti, Antonio Garofalo, and Francesca Aiello. "Triazolopyrimidinium salts: discovery of a new class of agents for cancer therapy." Future Medicinal Chemistry 12, no. 5 (March 2020): 387–402. http://dx.doi.org/10.4155/fmc-2019-0317.
Повний текст джерелаShah, Tariq A., Zubair Ahmad, Niyaz A. Mir, M. Muneer, Nigam P. Rath, and 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, no. 12 (2016): 9437. http://dx.doi.org/10.1039/c6ra90004f.
Повний текст джерелаArgăseală, 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, no. 3 (January 24, 2022): 765. http://dx.doi.org/10.3390/molecules27030765.
Повний текст джерелаNassar, 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, and 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, no. 23 (2022): 14865–82. http://dx.doi.org/10.1039/d2ra01968j.
Повний текст джерелаFan, Ning-Juan, Yuan-feng Li, Shuang Liang, and 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, no. 7 (July 2017): 413–15. http://dx.doi.org/10.3184/174751917x14967701767003.
Повний текст джерелаŁakomska, Iwona, Dariusz Śmiłowicz, Mateusz Jakubowski, Jerzy Sitkowski, and Andrzej Wojtczak. "Platinum(II) Complexes with Bulky Disubstitute Triazolopyrimidines as Promising Materials for Anticancer Agents." Materials 13, no. 23 (November 24, 2020): 5312. http://dx.doi.org/10.3390/ma13235312.
Повний текст джерелаHossain, M. I., and M. M. H. Bhuiyan. "Synthesis and Antimicrobial Activities of Some New Thieno and Furopyrimidine Derivatives." Journal of Scientific Research 1, no. 2 (April 23, 2009): 317–25. http://dx.doi.org/10.3329/jsr.v1i2.2299.
Повний текст джерелаTang, Caifei, Zhiming Li, and 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 (November 25, 2013): 2629–34. http://dx.doi.org/10.3762/bjoc.9.298.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаЧастини книг з теми "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." In Synthesis and Chemistry of Agrochemicals III, 10–16. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch002.
Повний текст джерелаKleschick, 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." In Synthesis and Chemistry of Agrochemicals III, 17–25. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch003.
Повний текст джерелаCostales, Mark J., William A. Kleschick, and B. Clifford Gerwick. "N-(Substituted-2-fluorophenyl)- andN-(Substituted-2-trifluoromethylphenyl)-1,2,4-triazolo-[1,5-a]pyrimidine-2-sulfonanilides." In Synthesis and Chemistry of Agrochemicals III, 26–33. Washington, DC: American Chemical Society, 1992. http://dx.doi.org/10.1021/bk-1992-0504.ch004.
Повний текст джерелаPardasani, R. T., and P. Pardasani. "Magnetic properties of bromine-bridged copper(II) dimer with 5,7-dimethyl[1,2,4-triazolo(1,5-α)]pyrimidine." In 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.
Повний текст джерелаPardasani, R. T., and P. Pardasani. "Magnetic properties of trans-aquatrichlorobis-(5, 7-dimethyl[1, 2, 4]triazolo[1, 5-a]pyrimidine-N3)-ruthenium(III) monohydrate." In 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.
Повний текст джерела"Kap. 2: Azapurine, Formamid als „Wunderreagenz“, Purinsynthese und Dimethylformamid/DimethylsulfatKomplexe." In Von Aromaten und Heterocyclen zur Bio- und Nanotechnologie, 39–52. GNT-Verlag GmbH, 2023. http://dx.doi.org/10.47261/1551-2.
Повний текст джерелаFischer, Gunther. "Recent Progress in 1,2,4-Triazolo[1,5-a]pyrimidine Chemistry." In Advances in Heterocyclic Chemistry, 143–219. Elsevier, 2007. http://dx.doi.org/10.1016/s0065-2725(07)95003-5.
Повний текст джерелаFischer, Gunther. "Recent advances in 1,2,4-triazolo[1,5-a]pyrimidine chemistry." In Advances in Heterocyclic Chemistry, 1–101. Elsevier, 2019. http://dx.doi.org/10.1016/bs.aihch.2018.10.002.
Повний текст джерелаLauria, Antonino, Chiara Patella, Patrizia Diana, Paola Barraja, Alessandra Montalbano, Gaetano Dattolo, Girolamo Cirrincione, and 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." In 19th International Congress on Heterocyclic Chemistry, 224. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50216-1.
Повний текст джерелаТези доповідей конференцій з теми "TRIAZOLO-PYRIMIDINE"
Scapin, Elisandra, Lilian Buriol, Taiana Scalco München, Clarissa Piccinin Frizzo, and Marcos A. P. Martins. "Synthesis of 1,2,4-Triazolo[1,5-a]pyrimidine Supported under Ultrasound Irradiation." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20131012143813.
Повний текст джерелаScapin, Elisandra, Lilian Buriol, Taiana Scalco München, Clarissa Piccinin Frizzo, Mara Marzari, and Marcos A. P. Martins. "Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0028-1.
Повний текст джерелаLyapustin, D. N., E. N. Ulomsky, E. K. Voinkov, and 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." In 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.
Повний текст джерелаGharib, Ali, Mina Roshani, and 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." In The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00169.
Повний текст джерела