Artículos de revistas sobre el tema "TRIAZOLO-TRIAZINE"
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Wang, Qian, Yanli Shao y Ming Lu. "Amino-tetrazole functionalized fused triazolo-triazine and tetrazolo-triazine energetic materials". Chemical Communications 55, n.º 43 (2019): 6062–65. http://dx.doi.org/10.1039/c9cc01777a.
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 completoNavarro, Amparo, M. Paz Fernández-Liencres, Gregorio García, José M. Granadino-Roldán y Manuel Fernández-Gómez. "A DFT approach to the charge transport related properties in columnar stacked π-conjugated N-heterocycle cores including electron donor and acceptor units". Physical Chemistry Chemical Physics 17, n.º 1 (2015): 605–18. http://dx.doi.org/10.1039/c4cp04220d.
Texto completoBernat, Zofia, Anna Szymanowska, Mateusz Kciuk, Katarzyna Kotwica-Mojzych y Mariusz Mojzych. "Review of the Synthesis and Anticancer Properties of Pyrazolo[4,3-e][1,2,4]triazine Derivatives". Molecules 25, n.º 17 (29 de agosto de 2020): 3948. http://dx.doi.org/10.3390/molecules25173948.
Texto completoHojo, Ryoga, Don M. Mayder y Zachary M. Hudson. "Donor–acceptor materials exhibiting deep blue emission and thermally activated delayed fluorescence with tris(triazolo)triazine". Journal of Materials Chemistry C 9, n.º 40 (2021): 14342–50. http://dx.doi.org/10.1039/d1tc03480d.
Texto completoHojo, Ryoga, Don M. Mayder y Zachary M. Hudson. "Donor–acceptor materials exhibiting deep blue emission and thermally activated delayed fluorescence with tris(triazolo)triazine". Journal of Materials Chemistry C 9, n.º 40 (2021): 14342–50. http://dx.doi.org/10.1039/d1tc03480d.
Texto completoHundemer, Fabian, Ettore Crovini, Yoshimasa Wada, Hironori Kaji, Stefan Bräse y Eli Zysman-Colman. "Tris(triazolo)triazine-based emitters for solution-processed blue thermally activated delayed fluorescence organic light-emitting diodes". Materials Advances 1, n.º 8 (2020): 2862–71. http://dx.doi.org/10.1039/d0ma00659a.
Texto completoFang, Zhou, Shengyue Wang, Junxu Liao, Xinrui Chen, Yuanyuan Zhu, Weiguo Zhu y Yafei Wang. "Asymmetric sky-blue thermally-activated delayed fluorescence emitters bearing tris(triazolo)triazine moiety for solution-processable organic light-emitting diodes". Journal of Materials Chemistry C 10, n.º 12 (2022): 4837–44. http://dx.doi.org/10.1039/d1tc05372h.
Texto completoAnikin, Oleg V., Nikita E. Leonov, Michael S. Klenov, Aleksandr M. Churakov, Alexey A. Voronin, Nikita V. Muravyev, Yurii A. Strelenko, Ivan V. Fedyanin y Vladimir A. Tartakovsky. "An Energetic (Nitro-NNO -azoxy)triazolo-1,2,4-triazine". European Journal of Organic Chemistry 2019, n.º 26 (13 de junio de 2019): 4189–95. http://dx.doi.org/10.1002/ejoc.201900314.
Texto completoMolina, Pedro, Mateo Alajar地, Ma Jes徭 P屍ez de Vega y Antonio L用ez. "Preparation of [1,2,4]Triazolo[5,1-c][1,2,4]triazine Derivatives from 3,4-Diamino[1,2,4]triazine". HETEROCYCLES 29, n.º 8 (1989): 1607. http://dx.doi.org/10.3987/com-89-5056.
Texto completoPiercey, Davin G., David E. Chavez, Brian L. Scott, Greg H. Imler y Damon A. Parrish. "An Energetic Triazolo-1,2,4-Triazine and its N-Oxide". Angewandte Chemie International Edition 55, n.º 49 (9 de noviembre de 2016): 15315–18. http://dx.doi.org/10.1002/anie.201608723.
Texto completoPiercey, Davin G., David E. Chavez, Brian L. Scott, Greg H. Imler y Damon A. Parrish. "An Energetic Triazolo-1,2,4-Triazine and its N-Oxide". Angewandte Chemie 128, n.º 49 (9 de noviembre de 2016): 15541–44. http://dx.doi.org/10.1002/ange.201608723.
Texto completoAbdel-Rahman, Reda M., Abdulrahman S. Alharbi, Nawaa A. Alshammari y Yousuf O. Adnan. "Design, Synthesis and Molluscicidal Activity of New Phosphorus Compounds Bearing Fluorine Substituted 1,2,4-Triazolo[3,2-c][1,2,4]triazine Derivatives". Letters in Organic Chemistry 17, n.º 3 (19 de febrero de 2020): 184–90. http://dx.doi.org/10.2174/1570178616666190718120953.
Texto completoHeravi, Majid M., Naser Montazeri, Mohammad Rahimizadeh, Mehdi Bakavoli y Mitra Ghassemzadeh. "Synthesis of 1,2,4-triazolo[1,5-d]-1,2,4-triazine-5-thiones". Journal of Heterocyclic Chemistry 42, n.º 5 (julio de 2005): 1021–25. http://dx.doi.org/10.1002/jhet.5570420544.
Texto completoKumar, Dheeraj, Gregory H. Imler, Damon A. Parrish y Jean'ne M. Shreeve. "A Highly Stable and Insensitive Fused Triazolo-Triazine Explosive (TTX)". Chemistry - A European Journal 23, n.º 8 (21 de diciembre de 2016): 1743–47. http://dx.doi.org/10.1002/chem.201604919.
Texto completoEpishina, Margarita A., Alexander S. Kulikov y Leonid L. Fershtat. "Revisiting the Synthesis of Functionally Substituted 1,4-Dihydrobenzo[e][1,2,4]triazines". Molecules 27, n.º 8 (15 de abril de 2022): 2575. http://dx.doi.org/10.3390/molecules27082575.
Texto completoBianchi, Mario, Alina Butti y Jacques Perronnet. "A new heterocyclic structure. The [1,2,3]triazolo[1,5-d][1,2,4]triazine". Journal of Heterocyclic Chemistry 25, n.º 3 (mayo de 1988): 743–50. http://dx.doi.org/10.1002/jhet.5570250309.
Texto completoFahim, Asmaa, Ahmad Farag, Mohamed Shaaban y Eman Ragab. "Microwave Assisted Synthesis of Pyrazolo[1,5-a]pyrimidine, Triazolo[1,5-a]pyrimidine, Pyrimido[1,2-a]benzimdazole, Triazolo[5,1-c][1,2,4]triazine and Imidazo[2,1-c][1,2,4]triazine". Current Microwave Chemistry 5, n.º 2 (8 de enero de 2019): 111–19. http://dx.doi.org/10.2174/2213335605666180425144009.
Texto completoAkahoshi, Fumihiko, Shinji Takeda, Takehiro Okada, Masahiko Kajii, Hiroko Nishimura, Masanori Sugiura, Yoshihisa Inoue et al. "Synthesis and Pharmacological Activity of Triazolo[1,5-a]triazine Derivatives Inhibiting Eosinophilia". Journal of Medicinal Chemistry 41, n.º 16 (julio de 1998): 2985–93. http://dx.doi.org/10.1021/jm970759u.
Texto completoMironovich, L. M., M. A. Ivanov y E. P. Koval'chuk. "ChemInform Abstract: Synthesis of 8-tert-Butyl-9-oxo-1,2,4-triazolo[4,5-b]-1,2,4-triazolo [3,4-c]-1,2,4-triazine." ChemInform 33, n.º 32 (20 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200232154.
Texto completoEl-Shehry, M. F., F. A. A. El-Hag y E. F. Ewies. "Synthesis and Antimicrobial Study of New Fused Thiazolo[3,2-b]triazine, Triazolo[4,3-b]triazine, and 1,2,4-Triazinone Derivatives". Russian Journal of Organic Chemistry 56, n.º 1 (enero de 2020): 129–36. http://dx.doi.org/10.1134/s1070428020010200.
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 completoEzema, B. E., L. E. S. Akpanisi, C. G. Ezema y A. E. Onoabedje. "A New Method of Dimroth Rearrangement in Fused Triazolo[1,5-d]-1,2,4-triazine". Journal of Heterocyclic Chemistry 52, n.º 5 (31 de julio de 2014): 1411–14. http://dx.doi.org/10.1002/jhet.2252.
Texto completoKurella, M. G., L. G. Vorontsova, A. R. Amamchyan y V. A. Dorokhov. "Crystal and molecular structure of 7-phenyl-1,2,4-triazolo[1,5-a]-1,3,5-triazine". Bulletin of the Russian Academy of Sciences Division of Chemical Science 41, n.º 6 (junio de 1992): 1084–86. http://dx.doi.org/10.1007/bf00866591.
Texto completoKhalil, Mohamed A., Samia M. Sayed y Mohamed A. Raslan. "Synthesis of New Pyrazolo[5,1-c]triazine, Triazolo[5,1-c]triazine, Triazino[4,3-b]indazole and Benzimidazo[2,1-c]triazine Derivatives Incorporating Chromen-2-one Moiety". Journal of the Korean Chemical Society 57, n.º 5 (20 de octubre de 2013): 612–17. http://dx.doi.org/10.5012/jkcs.2013.57.5.612.
Texto completoDeeb, Ali, Medhat El-Mobayed, Abdel Naby Essawy, Adel Abd El-Hamid y Atef Mohamid Abd El-Hamid. "Heterocyclic synthesis from 3-amino-4-cyanopyrazole". Collection of Czechoslovak Chemical Communications 55, n.º 3 (1990): 728–33. http://dx.doi.org/10.1135/cccc19900728.
Texto completoKrutošíková, Alžbeta, Slavomír Mastik, Miloslava Dandárová y Antonín Lyčka. "Synthesis and Reactions of 8-Hydrazinofuro[2',3':4,5]pyrrolo-[1,2-d][1,2,4]triazines". Collection of Czechoslovak Chemical Communications 62, n.º 10 (1997): 1612–22. http://dx.doi.org/10.1135/cccc19971612.
Texto completoGomha, Sobhi y Hatem Abdel-Aziz. "Synthesis of new functionalized derivatives of indolo[2,3-e][1,2,4]-triazolo-[4,5-b]-1,2,4-triazine". Journal of the Serbian Chemical Society 78, n.º 8 (2013): 1119–25. http://dx.doi.org/10.2298/jsc120914013g.
Texto completoNAITO, Y. y ET AL ET AL. "ChemInform Abstract: Synthesis and Pharmacological Activity of Triazolo[1,5-a]triazine Derivatives Inhibiting Eosinophilia." ChemInform 29, n.º 48 (18 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199848167.
Texto completoZhang, Guojie, Wei Hu, Jinchao Ma, Hongwei Yang y Guangbin Cheng. "Combining 5,6-fused triazolo-triazine with pyrazole: A novel energetic framework for heat-resistant explosive". Chemical Engineering Journal 426 (diciembre de 2021): 131297. http://dx.doi.org/10.1016/j.cej.2021.131297.
Texto completoQu, Yanyang. "Synthesis and Properties for Benzotriazole Nitrogen Oxides (BTzO) and Tris[1,2,4]triazolo[1,3,5]triazine Derivatives". International Journal of Materials Science and Applications 7, n.º 2 (2018): 49. http://dx.doi.org/10.11648/j.ijmsa.20180702.13.
Texto completoBera, Hriday, Anton V. Dolzhenko, Lingyi Sun, Sayan Dutta Gupta y Wai-Keung Chui. "Synthesis andin vitroEvaluation of 1,2,4-Triazolo[1,5-a][1,3,5]triazine Derivatives as Thymidine Phosphorylase Inhibitors". Chemical Biology & Drug Design 82, n.º 3 (22 de agosto de 2013): 351–60. http://dx.doi.org/10.1111/cbdd.12171.
Texto completoAbdelrehim, El-sayed M. y Doaa S. El-Sayed. "A New Synthesis of Poly Heterocyclic Compounds Containing [1,2,4]triazolo and [1,2,3,4]tetrazolo Moieties and their DFT Study as Expected Anti-cancer Reagents". Current Organic Synthesis 17, n.º 3 (9 de junio de 2020): 211–23. http://dx.doi.org/10.2174/1570179417666200226092516.
Texto completoZohdi, Hussein F. "Reactions with 3-Amino-5-trifluoromethyl[1,2,4]-triazole: A Convenient Route to Fluorinated Triazolo[1,5-c]thiadiazine, Triazolo[1,5-a]triazine, Thiazoles and Thiadiazoles". Journal of Chemical Research, n.º 9 (1998): 536–37. http://dx.doi.org/10.1039/a802034e.
Texto completoEl-Sayed, Wael A., Ibrahim F. Nassar y Adel A. H. Abdel-Rahman. "Synthesis and antitumor activity of new 1,2,4-triazine and [1,2,4]triazolo[4,3-b][1,2,4]triazine derivatives and their thioglycoside and acyclic C-nucleoside analogs". Journal of Heterocyclic Chemistry 48, n.º 1 (10 de septiembre de 2010): 135–43. http://dx.doi.org/10.1002/jhet.522.
Texto completoHajri, A. y L. Marzouki. "Easy Strategy for the Synthesis of New 5,6-Dihydro-[1,2,4]triazolo[4,3-a][1,3,5]triazine Derivatives". Russian Journal of Organic Chemistry 55, n.º 9 (septiembre de 2019): 1394–98. http://dx.doi.org/10.1134/s1070428019090203.
Texto completoHAJRI, A. y L. MARZOUKI. "EASY STRATEGY FOR THE SYNTHESIS OF NEW 5,6-DIHYDRO[1,2,4]TRIAZOLO[4,3-A][1,3,5]TRIAZINE DERIVATIVES". Журнал органической химии 55, n.º 9 (septiembre de 2019): 1475. http://dx.doi.org/10.1134/s0514749219090222.
Texto completoVu, Chi B., Bo Peng, Gnanasambandam Kumaravel, Glenn Smits, Xiaowei Jin, Deepali Phadke, Thomas Engber et al. "Piperazine Derivatives of [1,2,4]Triazolo[1,5-a][1,3,5]triazine as Potent and Selective Adenosine A2aReceptor Antagonists". Journal of Medicinal Chemistry 47, n.º 17 (agosto de 2004): 4291–99. http://dx.doi.org/10.1021/jm0498405.
Texto completoF. Zohdi, Hussein. "Reactions with 3-Amino-5-trifluoromethyl-1,2,4-triazole: a Simple Route to Fluorinated Poly-substituted Triazolo[1,5-a]pyrimidine and Triazolo[5,1-c]triazine Derivatives". Journal of Chemical Research, n.º 11 (1997): 392. http://dx.doi.org/10.1039/a701093a.
Texto completoM. Farag, Ahmad, Mohamed R. Shaaban y Tamer S. Saleh. "An Efficient Single Step Synthesis of Pyridazine, Pyrazolo[5,1-c]-1,2,4-triazine, 1,2,4-Triazolo[5,1-c]-1,2,4-triazine and 1,2,4-Triazino[4,3-a]benzimidazole Derivatives". HETEROCYCLES 78, n.º 3 (2009): 699. http://dx.doi.org/10.3987/com-08-11559.
Texto completoAbdel-Aziz, Hatem A., Nehal A. Hamdy, Issa M. I. Fakhr y Ahmad M. Farag. "Synthesis of some novel pyrazolo[1,5-a]pyrimidine, 1,2,4-triazolo[1,5-a]pyrimidine, pyrido[2,3-d]pyrimidine, pyrazolo[5,1-c]-1,2,4-triazine and 1,2,4-triazolo[5,1-c]-1,2,4-triazine derivatives incorporating a thiazolo[3,2-a]benzimidazole moiety". Journal of Heterocyclic Chemistry 45, n.º 4 (julio de 2008): 1033–37. http://dx.doi.org/10.1002/jhet.5570450413.
Texto completoKruglenko, V. P., V. P. Gnidets y M. V. Povstyanoi. "Synthesis of 2-methyl-1,2,4-triazolo[4,3-d]-1,2,4-triazino[2,3-a]-benzimidazole and 2-methyl-9-phenylimidazo[1,2-b]-1,2,4-triazolo[4,3-d]-1,2,4-triazine". Chemistry of Heterocyclic Compounds 36, n.º 1 (enero de 2000): 103–4. http://dx.doi.org/10.1007/bf02256854.
Texto completoZohdi, Hussein F. "ChemInform Abstract: Reactions with 3-Amino-5-trifluoromethyl[1,2,4]triazole: A Convenient Route to Fluorinated Triazolo[1,5-c]thiadiazine, Triazolo[1,5-a]triazine, Thiazoles, and Thiadiazoles." ChemInform 30, n.º 12 (17 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199912144.
Texto completoLi Huixue, 李会学, 胥亨霞 Xu Hengxia, 李志峰 Li Zhifeng, 王晓峰 Wang Xiaofeng, 董小宁 Dong Xiaoning, 袁昆 Yuan Kun, 朱元成 Zhu Yuancheng y 萧泰 Xiao Tai. "Crystal Structure and Photoelectric Properties of 3-Phenyl-6-(4-Methylphenyl)-1,2,4-Triazolo[4,3-b]-1,2,4-Triazine". Acta Optica Sinica 29, n.º 1 (2009): 236–43. http://dx.doi.org/10.3788/aos20092901.0236.
Texto completoMIYAMOTO, Yoshiko, Hitoshi KOHNO, Wolfgang PFLEIDERER, Peter BÖGER y Ko WAKABAYASHI. "Synthesis of 1, 2, 4-Triazolo[1, 5-a]-1, 3, 5-triazine Derivatives for Phytotoxic Activity". Journal of Pesticide Science 20, n.º 2 (1995): 119–28. http://dx.doi.org/10.1584/jpestics.20.119.
Texto completoEl-Mahdy, Kamelia M. "Facile synthesis of novel carbothioylbis[1,2,4]triazolo [4,3-a]pyrimidine and carbothioylbispyrimido[2,1-c] [1,2,4]triazine derivatives". Journal of Sulfur Chemistry 34, n.º 5 (12 de febrero de 2013): 539–45. http://dx.doi.org/10.1080/17415993.2013.765431.
Texto completoVu, Chi B., Deborah Pan, Bo Peng, Gnanasambandam Kumaravel, Glenn Smits, Xiaowei Jin, Deepali Phadke et al. "Novel Diamino Derivatives of [1,2,4]Triazolo[1,5-a][1,3,5]triazine as Potent and Selective Adenosine A2aReceptor Antagonists". Journal of Medicinal Chemistry 48, n.º 6 (marzo de 2005): 2009–18. http://dx.doi.org/10.1021/jm0498396.
Texto completoMontazeri, Nasser, Majid M. Heravi, Farzaneh Tajfirooz y Niousha Nazari. "Synthesis of bis[1,2,4]triazolo[4,3-b:1′,5′-d][1,2,4]triazine, a novel polynitrogenated heterocyclic system". Monatshefte für Chemie - Chemical Monthly 148, n.º 4 (17 de agosto de 2016): 691–94. http://dx.doi.org/10.1007/s00706-016-1810-y.
Texto completoMIRONOVICH, L. M. "ChemInform Abstract: Synthesis of 3-Hydrazino-6-tert-butyl-1,2,4-triazolo(3,4-c)-1,2,4- triazine-5-one." ChemInform 26, n.º 25 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199525170.
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