Статті в журналах з теми "TRIAZOLO-PYRIMIDINE"
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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 джерелаHempel, Ute, Eberhard Lippmann, and Ernst Tenor. "1,2,4-Triazolo [1,5-a] pyrimidine, Darstellung 7-aminsubstituierter 6-Nitro-1,2,4-triazolo[1,5-a]-pyrimidine." Zeitschrift für Chemie 30, no. 5 (August 31, 2010): 170. http://dx.doi.org/10.1002/zfch.19900300505.
Повний текст джерелаAhmed, Essam K., Johannes Fröhlich, and Fritz Sauter. "Fusion Reactions of N-Heterocyclic Moieties to Thiopyrano[4',3':4,5]thieno[2,3-d]pyrimidines." Collection of Czechoslovak Chemical Communications 61, no. 1 (1996): 147–54. http://dx.doi.org/10.1135/cccc19960147.
Повний текст джерелаMounir, Salem, Magda Marzouk, and Naglaa Mahmoud. "Synthesis of various fused pyrimidine rings with their pharmacological and antimicrobial evaluation." Journal of the Serbian Chemical Society 79, no. 9 (2014): 1059–73. http://dx.doi.org/10.2298/jsc130528016m.
Повний текст джерелаYu, Guang-Xi, Ying Hu, Wei-Xin Zhang, Xin-Yi Tian, Sai-Yang Zhang, Yan Zhang, Shuo Yuan, and Jian Song. "Design, Synthesis and Biological Evaluation of [1,2,4]Triazolo[1,5-a]pyrimidine Indole Derivatives against Gastric Cancer Cells MGC-803 via the Suppression of ERK Signaling Pathway." Molecules 27, no. 15 (August 5, 2022): 4996. http://dx.doi.org/10.3390/molecules27154996.
Повний текст джерелаSalas, Juan M., Miguel Quirós, Mohammad Abul Haj, Rosa Magán, Clotilde Marín, Manuel Sáchez-Moreno, and René Faure. "Activity of Pt(II) and Ru(III) Triazolopyrimidine Complexes Against Parasites of the Genus Leishmania, Trypanosomas and Phytomonas." Metal-Based Drugs 8, no. 3 (January 1, 2001): 119–24. http://dx.doi.org/10.1155/mbd.2001.119.
Повний текст джерелаAbdel-Hafez, Shams H., Ragaa A. Ahmed, Mohamed A. Abdel-Azim, and Khairy M. Hassan. "Selenium containing Heterocycles: Part 1. Synthesis of Some New Substituted Pyrido[3′,2′:4,5]selenolo[3,2-d]pyrimidines and Related Fused Tetracyclic Systems." Journal of Chemical Research 2007, no. 10 (October 2007): 580–84. http://dx.doi.org/10.3184/030823407x25506.
Повний текст джерелаOdabaşoğlu, Mustafa, and Orhan Büyükgüngör. "5,7-Dimethyl-1,2,4-triazolo[1,5-a]pyrimidine." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 10, 2006): o1310—o1311. http://dx.doi.org/10.1107/s1600536806008166.
Повний текст джерелаHempel, Ute, Eberhard Lippmann, and Ernst Tenor. "1,2,4-Triazolo [1,5-a] pyrimidine: Reaktionen von Amino-und Hydrazino-1,2,4-triazolo[1,5-a]pyrimidine mit Dimethylformamid-dimethylacetal." Zeitschrift für Chemie 30, no. 9 (August 31, 2010): 320–21. http://dx.doi.org/10.1002/zfch.19900300905.
Повний текст джерелаBiagi, Giuliana, Irene Giorgi, Oreste Livi, Federica Pacchini, and Valerio Scartoni. "New 1,2,3-triazolo[4,5-e]1,2,4-triazolo[4,3-c]pyrimidine derivatives II." Journal of Heterocyclic Chemistry 39, no. 5 (September 2002): 885–88. http://dx.doi.org/10.1002/jhet.5570390505.
Повний текст джерелаOgorodnik, A. G., V. A. Yanchenko, L. S. Bobkova, N. M. Seredinska та A. M. Demchenko. "Synthesis and anаlgеsic activity 5-methyl-3-aryl[1,2,4]triazolo[4,3-a]pyrimidin-7-oles derivatives". Farmatsevtychnyi zhurnal, № 2 (14 серпня 2018): 55–61. http://dx.doi.org/10.32352/0367-3057.2.17.07.
Повний текст джерелаAbdelhamid, Abdou O., and Sobhi M. Gomha. "Synthesis of New Pyrazolo[1,5-a]pyrimidine, Triazolo[4,3-a]pyrimidine Derivatives, and Thieno[2,3-b]pyridine Derivatives from Sodium 3-(5-Methyl-1-phenyl-1H-pyrazol-4-yl)-3-oxoprop-1-en-1-olate." Journal of Chemistry 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/327095.
Повний текст джерелаŁakomska, Iwona, Magdalena Babinska, Andrzej Wojtczak, Anna Kozakiewicz, Jerzy Sitkowski, and Andrzej A. Jarzęcki. "Experimental and theoretical investigation of the complexation of 5-methyl-7-isobutyl-1,2,4-triazolo[1,5-a]pyrimidine with platinum(ii) ions." New Journal of Chemistry 41, no. 15 (2017): 7775–82. http://dx.doi.org/10.1039/c7nj01112a.
Повний текст джерелаAttanzio, Alessandro, Simone D’Agostino, Rosalia Busà, Anna Frazzitta, Simona Rubino, Maria Assunta Girasolo, Piera Sabatino, and Luisa Tesoriere. "Cytotoxic Activity of Organotin(IV) Derivatives with Triazolopyrimidine Containing Exocyclic Oxygen Atoms." Molecules 25, no. 4 (February 15, 2020): 859. http://dx.doi.org/10.3390/molecules25040859.
Повний текст джерелаShah, A. M., and A. J. Rojivadiya. "An Expeditious Synthesis of 1,2,4-Triazolo[1,5-a]Pyrimidine." International Letters of Chemistry, Physics and Astronomy 51 (May 2015): 1–4. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.51.1.
Повний текст джерелаShah, A. M., and A. J. Rojivadiya. "An Expeditious Synthesis of 1,2,4-Triazolo[1,5-<i>a</i>]Pyrimidine." International Letters of Chemistry, Physics and Astronomy 51 (May 15, 2015): 1–4. http://dx.doi.org/10.56431/p-p4100a.
Повний текст джерелаFizer, O. I., M. M. Fizer, A. O. Kryvoviaz, and 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, no. 2 (February 10, 2022): 55–62. http://dx.doi.org/10.24144/2414-0260.2021.2.55-62.
Повний текст джерелаOtero, Iran, Holger Feist, Dirk Michalik, Manfred Michalik, José Quincoces та Klaus Peseke. "Synthesis of Iso-C-nucleoside Analogues from 1-(Methyl 2-O-benzyl-4,6- O-benzylidene-3-deoxy-α-D-altropyranosid-3-yl)but-3-yn-2-ones". Zeitschrift für Naturforschung B 60, № 11 (1 листопада 2005): 1175–85. http://dx.doi.org/10.1515/znb-2005-1110.
Повний текст джерелаMIYAMOTO, YOSHIKO. "Synthesis of (1,2,4)triazolo(1,5-c)pyrimidine derivatives." CHEMICAL & PHARMACEUTICAL BULLETIN 33, no. 7 (1985): 2678–87. http://dx.doi.org/10.1248/cpb.33.2678.
Повний текст джерелаAbarca, Belén, Rafael Ballesteros, Mimoun Chadlaoui, Javier Miralles, José Vicente Murillo, and Dimas Colonna. "The chemistry of [1,2,3]triazolo[1,5- c ]pyrimidine." Tetrahedron 57, no. 51 (December 2001): 10111–17. http://dx.doi.org/10.1016/s0040-4020(01)01053-5.
Повний текст джерелаFizer, Maksym, and Mikhailo Slivka. "Synthesis of [1,2,4]triazolo[1,5-a]pyrimidine (microreview)." Chemistry of Heterocyclic Compounds 52, no. 3 (March 2016): 155–57. http://dx.doi.org/10.1007/s10593-016-1851-5.
Повний текст джерелаChechina, Natal’ya V., Nadezhda N. Kolos, Irina V. Omelchenko, and Vladimir I. Musatov. "Synthesis of functionalized triazolo[1,5-a]pyrimidine derivatives." Chemistry of Heterocyclic Compounds 54, no. 1 (January 2018): 58–62. http://dx.doi.org/10.1007/s10593-018-2230-1.
Повний текст джерелаEl Ashry, E. S. H., Y. El Kilany, N. Rashed, A. Mousaad, and H. Assafir. "Synthesis and Dimroth Rearrangement of 6-Cyano-l,2,4-triazolo- [4,3-a]pyrimidin-5- and 7-ones. A Novel Alkylation with Orthoesters and a New Participation of the Cyano Group in the Rearrangement." Zeitschrift für Naturforschung B 53, no. 10 (October 1, 1998): 1203–12. http://dx.doi.org/10.1515/znb-1998-1017.
Повний текст джерелаSwelam, Samira, Abd El-Salam, and Magdi Zaki. "Synthesis of some pyrazolo[3,4-d]pyrimidines and their fused triazole and tetrazole derivatives." Journal of the Serbian Chemical Society 64, no. 11 (1999): 655–62. http://dx.doi.org/10.2298/jsc9911655s.
Повний текст джерелаGami, Sagar P., Kalpesh V. Vilapara, Hasmukh R. Khunt, Jayesh S. Babariya, and Yogesh T. Naliapara. "Synthesis and Antimicrobal Activities of some Novel Triazolo[1,5-a]Pyrimidine Derivatives." International Letters of Chemistry, Physics and Astronomy 30 (March 2014): 127–34. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.30.127.
Повний текст джерелаGami, Sagar P., Kalpesh V. Vilapara, Hasmukh R. Khunt, Jayesh S. Babariya, and Yogesh T. Naliapara. "Synthesis and Antimicrobal Activities of some Novel Triazolo[1,5-a]Pyrimidine Derivatives." International Letters of Chemistry, Physics and Astronomy 30 (March 12, 2014): 127–34. http://dx.doi.org/10.56431/p-2r9pl7.
Повний текст джерелаSyrota, Natalia O., Sergiy V. Kemskiy, Lesya M. Saliyeva, and 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, no. 2 (July 20, 2022): 27–51. http://dx.doi.org/10.24959/ophcj.22.258512.
Повний текст джерелаSurdykowski, A., E. Szłyk, and S. Larsen. "5,7-Diphenyl[1,2,4]triazolo[1,5-a]pyrimidine at 122K." Acta Crystallographica Section C Crystal Structure Communications 55, no. 8 (August 15, 1999): 1337–39. http://dx.doi.org/10.1107/s0108270199004631.
Повний текст джерелаYavolovskii, A. A., E. I. Ivanov, A. V. Mazepa, and Yu E. Ivanov. "Synthesis of [1,2,3]Triazolo[4,5-d]pyrimidine 3-Oxides." Russian Journal of General Chemistry 73, no. 9 (September 2003): 1486–88. http://dx.doi.org/10.1023/b:rugc.0000016004.71832.bb.
Повний текст джерелаFettouhi, M., A. Boukhari, B. El Otmani, and E. M. Essassi. "7-Ethoxycarbonylmethyl-5-methyl-1,2,4-triazolo[1,5-a]pyrimidine." Acta Crystallographica Section C Crystal Structure Communications 52, no. 4 (April 15, 1996): 1031–32. http://dx.doi.org/10.1107/s0108270195013680.
Повний текст джерелаSalas, Juan M., M. Angustias Romero, M. Purificación Sánchez, and Miguel Quirós. "Metal complexes of [1,2,4]triazolo-[1,5-a]pyrimidine derivatives." Coordination Chemistry Reviews 193-195 (October 1999): 1119–42. http://dx.doi.org/10.1016/s0010-8545(99)00004-1.
Повний текст джерелаHori, Mikio, Kiyomi Tanaka, Tadashi Kataoka, Hiroshi Shimizu, Eiji Imai, Kazuhiko Kimura, and Yoshinobu Hashimoto. "Thermolysis of [1,2,4]triazolo[1,5-a]pyrimidine n-ylides." Tetrahedron Letters 26, no. 10 (January 1985): 1321–22. http://dx.doi.org/10.1016/s0040-4039(00)94882-2.
Повний текст джерелаRusinov, V. L., T. L. Pilicheva, and O. N. Chupakhin. "Synthesis of indolyl derivatives of triazolo[1,5-a]pyrimidine." Chemistry of Heterocyclic Compounds 21, no. 9 (September 1985): 1058. http://dx.doi.org/10.1007/bf00515036.
Повний текст джерелаLokaj, Jan, Viktor Kettmann, Svetozár Katuščák, Petra Černuchová, Viktor Milata, and Fridrich Gregáň. "5-Methyl-1,2,4-triazolo[1,5-a]pyrimidine-6-carbonitrile." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 8, 2006): o1252—o1253. http://dx.doi.org/10.1107/s1600536806007240.
Повний текст джерелаBrazeau, Jean-Francois, and Gerard Rosse. "Triazolo[4,5-d]pyrimidine Derivatives as Inhibitors of GCN2." ACS Medicinal Chemistry Letters 5, no. 4 (February 12, 2014): 282–83. http://dx.doi.org/10.1021/ml500052f.
Повний текст джерелаGründler, Peter, Waldemar Hofmann, and Gunther Fischer. "Die anodischen Polarogramme der symm.-Triazolo [1,5-a]pyrimidine." Zeitschrift für Chemie 14, no. 11 (September 1, 2010): 442. http://dx.doi.org/10.1002/zfch.19740141113.
Повний текст джерелаJaenecke, Günter, Lieselotte Meister, Lisa Dressel, Renate Richter, and Harry Voigt. "Synthese substituierter 3H,5H-1,2,4-Triazolo[1,5-a]pyrimidine." Zeitschrift für Chemie 29, no. 10 (August 31, 2010): 378–79. http://dx.doi.org/10.1002/zfch.19890291005.
Повний текст джерелаFischer, Gunther. "Synthese und Eigenschaften der s-Triazolo[1,5-a]pyrimidine." Zeitschrift für Chemie 30, no. 9 (August 31, 2010): 305–15. http://dx.doi.org/10.1002/zfch.19900300902.
Повний текст джерелаShankar, Ravi B., and R. Garth Pews. "Synthesis of 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides." Journal of Heterocyclic Chemistry 30, no. 1 (January 1993): 169–72. http://dx.doi.org/10.1002/jhet.5570300130.
Повний текст джерелаKleschick, William A., Mark J. Costales, Joseph E. Dunbar, Richard W. Meikle, William T. Monte, Norman R. Pearson, Sigrid W. Snider, and Anna P. Vinogradoff. "New herbicidal derivatives of 1,2,4-triazolo [1,5-a] pyrimidine." Pesticide Science 29, no. 3 (1990): 341–55. http://dx.doi.org/10.1002/ps.2780290309.
Повний текст джерелаDooley, Michael J., Ronald J. Quinn, Wyona C. Patalinghug, and Allan H. White. "Synthesis of a pyrimidine by elimination of nitrogen from a triazolo[4,5-d]pyrimidine." Tetrahedron Letters 31, no. 42 (January 1990): 6103–4. http://dx.doi.org/10.1016/s0040-4039(00)98041-9.
Повний текст джерела