Статті в журналах з теми "TRIAZOLO-TRIAZINE"
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Wang, Qian, Yanli Shao, and Ming Lu. "Amino-tetrazole functionalized fused triazolo-triazine and tetrazolo-triazine energetic materials." Chemical Communications 55, no. 43 (2019): 6062–65. http://dx.doi.org/10.1039/c9cc01777a.
Повний текст джерелаPathak, Suraj Kumar, Yepeng Xiang, Manli Huang, Taian Huang, Xiaosong Cao, He Liu, Guohua Xie, and 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, no. 26 (2020): 15523–29. http://dx.doi.org/10.1039/d0ra01925a.
Повний текст джерелаZeng, Qun, Yanyang Qu, Jinshan Li, and 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, no. 7 (2016): 5419–27. http://dx.doi.org/10.1039/c5ra22524h.
Повний текст джерелаNavarro, Amparo, M. Paz Fernández-Liencres, Gregorio García, José M. Granadino-Roldán та 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, № 1 (2015): 605–18. http://dx.doi.org/10.1039/c4cp04220d.
Повний текст джерелаBernat, Zofia, Anna Szymanowska, Mateusz Kciuk, Katarzyna Kotwica-Mojzych, and Mariusz Mojzych. "Review of the Synthesis and Anticancer Properties of Pyrazolo[4,3-e][1,2,4]triazine Derivatives." Molecules 25, no. 17 (August 29, 2020): 3948. http://dx.doi.org/10.3390/molecules25173948.
Повний текст джерелаHojo, Ryoga, Don M. Mayder, and 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, no. 40 (2021): 14342–50. http://dx.doi.org/10.1039/d1tc03480d.
Повний текст джерелаHojo, Ryoga, Don M. Mayder, and 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, no. 40 (2021): 14342–50. http://dx.doi.org/10.1039/d1tc03480d.
Повний текст джерелаHundemer, Fabian, Ettore Crovini, Yoshimasa Wada, Hironori Kaji, Stefan Bräse, and Eli Zysman-Colman. "Tris(triazolo)triazine-based emitters for solution-processed blue thermally activated delayed fluorescence organic light-emitting diodes." Materials Advances 1, no. 8 (2020): 2862–71. http://dx.doi.org/10.1039/d0ma00659a.
Повний текст джерелаFang, Zhou, Shengyue Wang, Junxu Liao, Xinrui Chen, Yuanyuan Zhu, Weiguo Zhu, and 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, no. 12 (2022): 4837–44. http://dx.doi.org/10.1039/d1tc05372h.
Повний текст джерелаAnikin, Oleg V., Nikita E. Leonov, Michael S. Klenov, Aleksandr M. Churakov, Alexey A. Voronin, Nikita V. Muravyev, Yurii A. Strelenko, Ivan V. Fedyanin, and Vladimir A. Tartakovsky. "An Energetic (Nitro-NNO -azoxy)triazolo-1,2,4-triazine." European Journal of Organic Chemistry 2019, no. 26 (June 13, 2019): 4189–95. http://dx.doi.org/10.1002/ejoc.201900314.
Повний текст джерелаMolina, Pedro, Mateo Alajar地, Ma Jes徭 P屍ez de Vega, and 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, no. 8 (1989): 1607. http://dx.doi.org/10.3987/com-89-5056.
Повний текст джерелаPiercey, Davin G., David E. Chavez, Brian L. Scott, Greg H. Imler, and Damon A. Parrish. "An Energetic Triazolo-1,2,4-Triazine and its N-Oxide." Angewandte Chemie International Edition 55, no. 49 (November 9, 2016): 15315–18. http://dx.doi.org/10.1002/anie.201608723.
Повний текст джерелаPiercey, Davin G., David E. Chavez, Brian L. Scott, Greg H. Imler, and Damon A. Parrish. "An Energetic Triazolo-1,2,4-Triazine and its N-Oxide." Angewandte Chemie 128, no. 49 (November 9, 2016): 15541–44. http://dx.doi.org/10.1002/ange.201608723.
Повний текст джерелаAbdel-Rahman, Reda M., Abdulrahman S. Alharbi, Nawaa A. Alshammari, and 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, no. 3 (February 19, 2020): 184–90. http://dx.doi.org/10.2174/1570178616666190718120953.
Повний текст джерелаHeravi, Majid M., Naser Montazeri, Mohammad Rahimizadeh, Mehdi Bakavoli, and Mitra Ghassemzadeh. "Synthesis of 1,2,4-triazolo[1,5-d]-1,2,4-triazine-5-thiones." Journal of Heterocyclic Chemistry 42, no. 5 (July 2005): 1021–25. http://dx.doi.org/10.1002/jhet.5570420544.
Повний текст джерелаKumar, Dheeraj, Gregory H. Imler, Damon A. Parrish, and Jean'ne M. Shreeve. "A Highly Stable and Insensitive Fused Triazolo-Triazine Explosive (TTX)." Chemistry - A European Journal 23, no. 8 (December 21, 2016): 1743–47. http://dx.doi.org/10.1002/chem.201604919.
Повний текст джерелаEpishina, Margarita A., Alexander S. Kulikov, and Leonid L. Fershtat. "Revisiting the Synthesis of Functionally Substituted 1,4-Dihydrobenzo[e][1,2,4]triazines." Molecules 27, no. 8 (April 15, 2022): 2575. http://dx.doi.org/10.3390/molecules27082575.
Повний текст джерелаBianchi, Mario, Alina Butti, and Jacques Perronnet. "A new heterocyclic structure. The [1,2,3]triazolo[1,5-d][1,2,4]triazine." Journal of Heterocyclic Chemistry 25, no. 3 (May 1988): 743–50. http://dx.doi.org/10.1002/jhet.5570250309.
Повний текст джерелаFahim, Asmaa, Ahmad Farag, Mohamed Shaaban, and 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, no. 2 (January 8, 2019): 111–19. http://dx.doi.org/10.2174/2213335605666180425144009.
Повний текст джерелаAkahoshi, 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, no. 16 (July 1998): 2985–93. http://dx.doi.org/10.1021/jm970759u.
Повний текст джерелаMironovich, L. M., M. A. Ivanov, and 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, no. 32 (May 20, 2010): no. http://dx.doi.org/10.1002/chin.200232154.
Повний текст джерелаEl-Shehry, M. F., F. A. A. El-Hag, and 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, no. 1 (January 2020): 129–36. http://dx.doi.org/10.1134/s1070428020010200.
Повний текст джерелаFedotov, S. O., and 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, no. 3 (November 15, 2022): 227–34. http://dx.doi.org/10.14739/2409-2932.2022.3.263994.
Повний текст джерелаEzema, B. E., L. E. S. Akpanisi, C. G. Ezema, and A. E. Onoabedje. "A New Method of Dimroth Rearrangement in Fused Triazolo[1,5-d]-1,2,4-triazine." Journal of Heterocyclic Chemistry 52, no. 5 (July 31, 2014): 1411–14. http://dx.doi.org/10.1002/jhet.2252.
Повний текст джерелаKurella, M. G., L. G. Vorontsova, A. R. Amamchyan, and 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, no. 6 (June 1992): 1084–86. http://dx.doi.org/10.1007/bf00866591.
Повний текст джерелаKhalil, Mohamed A., Samia M. Sayed, and 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, no. 5 (October 20, 2013): 612–17. http://dx.doi.org/10.5012/jkcs.2013.57.5.612.
Повний текст джерелаDeeb, Ali, Medhat El-Mobayed, Abdel Naby Essawy, Adel Abd El-Hamid, and Atef Mohamid Abd El-Hamid. "Heterocyclic synthesis from 3-amino-4-cyanopyrazole." Collection of Czechoslovak Chemical Communications 55, no. 3 (1990): 728–33. http://dx.doi.org/10.1135/cccc19900728.
Повний текст джерелаKrutošíková, Alžbeta, Slavomír Mastik, Miloslava Dandárová, and 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, no. 10 (1997): 1612–22. http://dx.doi.org/10.1135/cccc19971612.
Повний текст джерелаGomha, Sobhi, and 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, no. 8 (2013): 1119–25. http://dx.doi.org/10.2298/jsc120914013g.
Повний текст джерелаNAITO, Y., and ET AL ET AL. "ChemInform Abstract: Synthesis and Pharmacological Activity of Triazolo[1,5-a]triazine Derivatives Inhibiting Eosinophilia." ChemInform 29, no. 48 (June 18, 2010): no. http://dx.doi.org/10.1002/chin.199848167.
Повний текст джерелаZhang, Guojie, Wei Hu, Jinchao Ma, Hongwei Yang, and Guangbin Cheng. "Combining 5,6-fused triazolo-triazine with pyrazole: A novel energetic framework for heat-resistant explosive." Chemical Engineering Journal 426 (December 2021): 131297. http://dx.doi.org/10.1016/j.cej.2021.131297.
Повний текст джерелаQu, 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, no. 2 (2018): 49. http://dx.doi.org/10.11648/j.ijmsa.20180702.13.
Повний текст джерелаBera, Hriday, Anton V. Dolzhenko, Lingyi Sun, Sayan Dutta Gupta, and 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, no. 3 (August 22, 2013): 351–60. http://dx.doi.org/10.1111/cbdd.12171.
Повний текст джерелаAbdelrehim, El-sayed M., and 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, no. 3 (June 9, 2020): 211–23. http://dx.doi.org/10.2174/1570179417666200226092516.
Повний текст джерелаZohdi, 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, no. 9 (1998): 536–37. http://dx.doi.org/10.1039/a802034e.
Повний текст джерелаEl-Sayed, Wael A., Ibrahim F. Nassar, and 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, no. 1 (September 10, 2010): 135–43. http://dx.doi.org/10.1002/jhet.522.
Повний текст джерелаHajri, A., and 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, no. 9 (September 2019): 1394–98. http://dx.doi.org/10.1134/s1070428019090203.
Повний текст джерелаHAJRI, A., and 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, no. 9 (September 2019): 1475. http://dx.doi.org/10.1134/s0514749219090222.
Повний текст джерелаVu, 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, no. 17 (August 2004): 4291–99. http://dx.doi.org/10.1021/jm0498405.
Повний текст джерелаF. 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, no. 11 (1997): 392. http://dx.doi.org/10.1039/a701093a.
Повний текст джерелаM. Farag, Ahmad, Mohamed R. Shaaban, and 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, no. 3 (2009): 699. http://dx.doi.org/10.3987/com-08-11559.
Повний текст джерелаAbdel-Aziz, Hatem A., Nehal A. Hamdy, Issa M. I. Fakhr, and 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, no. 4 (July 2008): 1033–37. http://dx.doi.org/10.1002/jhet.5570450413.
Повний текст джерелаKruglenko, V. P., V. P. Gnidets, and 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, no. 1 (January 2000): 103–4. http://dx.doi.org/10.1007/bf02256854.
Повний текст джерелаZohdi, 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, no. 12 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199912144.
Повний текст джерелаLi 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, and 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, no. 1 (2009): 236–43. http://dx.doi.org/10.3788/aos20092901.0236.
Повний текст джерелаMIYAMOTO, Yoshiko, Hitoshi KOHNO, Wolfgang PFLEIDERER, Peter BÖGER, and Ko WAKABAYASHI. "Synthesis of 1, 2, 4-Triazolo[1, 5-a]-1, 3, 5-triazine Derivatives for Phytotoxic Activity." Journal of Pesticide Science 20, no. 2 (1995): 119–28. http://dx.doi.org/10.1584/jpestics.20.119.
Повний текст джерелаEl-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, no. 5 (February 12, 2013): 539–45. http://dx.doi.org/10.1080/17415993.2013.765431.
Повний текст джерелаVu, 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, no. 6 (March 2005): 2009–18. http://dx.doi.org/10.1021/jm0498396.
Повний текст джерелаMontazeri, Nasser, Majid M. Heravi, Farzaneh Tajfirooz, and 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, no. 4 (August 17, 2016): 691–94. http://dx.doi.org/10.1007/s00706-016-1810-y.
Повний текст джерелаMIRONOVICH, 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, no. 25 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199525170.
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