Literatura académica sobre el tema "Triazole and tetrazole"
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Artículos de revistas sobre el tema "Triazole and tetrazole"
Suresh, Lingala, P. Sagar Vijay Kumar, T. Vinodkumar y G. V. P. Chandramouli. "Heterogeneous recyclable nano-CeO2 catalyst: efficient and eco-friendly synthesis of novel fused triazolo and tetrazolo pyrimidine derivatives in aqueous medium". RSC Advances 6, n.º 73 (2016): 68788–97. http://dx.doi.org/10.1039/c6ra16307f.
Texto completoChandrasekhar, Attoor, Venkatachalam Ramkumar y Sethuraman Sankararaman. "Palladium catalyzed carbonylative annulation of the C(sp2)–H bond of N,1-diaryl-1H-tetrazol-5-amines and N,4-diaryl-4H-triazol-3-amines to quinazolinones". Organic & Biomolecular Chemistry 16, n.º 44 (2018): 8629–38. http://dx.doi.org/10.1039/c8ob02516a.
Texto completoLysenko, Andrey B. "The heterobifunctional ligand 5-[4-(1,2,4-triazol-4-yl)phenyl]-1H-tetrazole and its role in the construction of a CdIImetal–organic chain structure". Acta Crystallographica Section C Crystal Structure Communications 68, n.º 10 (18 de septiembre de 2012): m291—m294. http://dx.doi.org/10.1107/s0108270112038498.
Texto completoPavlov, Dmitry, Taisiya Sukhikh, Evgeny Filatov y Andrei Potapov. "Facile Synthesis of 3-(Azol-1-yl)-1-adamantanecarboxylic Acids—New Bifunctional Angle-Shaped Building Blocks for Coordination Polymers". Molecules 24, n.º 15 (26 de julio de 2019): 2717. http://dx.doi.org/10.3390/molecules24152717.
Texto completoCiesielski, Witold y Anna Krenc. "Potentiometric Titration of Triazolethiols and Tetrazolethiols with Iodine in Alkaline Medium". Collection of Czechoslovak Chemical Communications 67, n.º 8 (2002): 1193–99. http://dx.doi.org/10.1135/cccc20021193.
Texto completoDioukhane, Khadim, Younas Aouine, Salaheddine Boukhssas, Asmae Nakkabi, Hassane Faraj y Anouar Alami. "Synthesis and Characterization of a Novel Biheterocyclic -amino Acid Precursor of the Triazole-Tetrazole Type, via the Copper (I) Catalyzed Alkyne-Azide Cycloaddition Reaction (CuAAC)". European Journal of Advanced Chemistry Research 2, n.º 2 (26 de marzo de 2021): 7–15. http://dx.doi.org/10.24018/ejchem.2021.2.2.53.
Texto completoZhao, Gang, Chunlin He, Haixiang Gao, Gregory H. Imler, Damon A. Parrish y Jean'ne M. Shreeve. "Improving the density and properties of nitrogen-rich scaffolds by the introduction of a C–NO2 group". New Journal of Chemistry 42, n.º 19 (2018): 16162–66. http://dx.doi.org/10.1039/c8nj03472a.
Texto completoTiwari, Vibha, Jacob T. Bingham, Shubham Vyas y Anand Singh. "Intermolecular fluoroamination of allenes towards substituted vinyl fluorides". Organic & Biomolecular Chemistry 18, n.º 44 (2020): 9044–49. http://dx.doi.org/10.1039/d0ob01697g.
Texto completoTang, Yongxing, Chunlin He, Gregory H. Imler, Damon A. Parrish y Jean'ne M. Shreeve. "Design and synthesis of N-methylene-C linked tetrazole and nitramino-1,2,4-triazole: an approach to promising energetic materials". Journal of Materials Chemistry A 4, n.º 36 (2016): 13923–29. http://dx.doi.org/10.1039/c6ta05057c.
Texto completoHamdan, Fatima, Fatemeh Tahoori y Saeed Balalaie. "Synthesis of novel cyclopeptides containing heterocyclic skeletons". RSC Advances 8, n.º 59 (2018): 33893–926. http://dx.doi.org/10.1039/c8ra03899f.
Texto completoTesis sobre el tema "Triazole and tetrazole"
Radies, Hendrik. "Tetrazole und Triazole als neuartige Oxidationsmittel in IR-Täuschkörpern". Diss., lmu, 2009. http://nbn-resolving.de/urn:nbn:de:bvb:19-113956.
Texto completoMadadi, Nikhil Reddy. "Synthesis and Biological Evaluation of Novel Resveratrol and Combretastatin A4 Derivatives as Potent Anti-Cancer Agents". UKnowledge, 2014. http://uknowledge.uky.edu/pharmacy_etds/42.
Texto completoSproll, Stefan Michael. "Investigation of Nitrogen-Rich Polymers based on tetrazoles and triazoles". Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-119590.
Texto completoBetzler, Franziska Maria. "Investigation of Nitrogen-Rich polymers based on cellulose, tetrazoles and triazoles". Diss., Ludwig-Maximilians-Universität München, 2013. http://nbn-resolving.de/urn:nbn:de:bvb:19-179281.
Texto completoBetzler, Franziska Maria [Verfasser] y Thomas M. [Akademischer Betreuer] Klapötke. "Investigation of Nitrogen-Rich polymers based on cellulose, tetrazoles and triazoles / Franziska Maria Betzler. Betreuer: Thomas M. Klapötke". München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2013. http://d-nb.info/1067055258/34.
Texto completoZhang, Yixin. "Design and Synthesis of a Series of Redox Active Tetrazine and Triazine Based Transition Metal Complexes". Thesis, Université d'Ottawa / University of Ottawa, 2018. http://hdl.handle.net/10393/37233.
Texto completoIhle, Andreas. "Synthese neuer makrocyclischer Triazolsysteme". Doctoral thesis, Universitätsbibliothek Chemnitz, 2006. http://nbn-resolving.de/urn:nbn:de:swb:ch1-200601537.
Texto completoPellegatti, Laurent. "Méthodologie en chimie hétérocyclique et application à la synthèse d'inhibiteurs de kinases". Thesis, Orléans, 2010. http://www.theses.fr/2010ORLE2046.
Texto completoCancer, one of the leading causes of death, represents today a major public health problem. Over the last few years, marine alkaloids represent a source of inspiration for chemists in order to obtain new anticancer drugs. For this purpose, as a part of our laboratory researches, analogues of marine alkaloids were synthesized possessing a tris-aromatic structure. We developed originals analogs of these alacaloïds formed by a central heterocycle core (1,2,4-triazine et imidazo[1,2-b][1,2,4,5]tetrazine) on wich is graft two arylic moiety variously substituted. Obtaining these compounds was also an opportunity to develop news synthetic methodologies. So a new Buchwald-Hartwig reaction type based on methylsulfanyl-1,2,4-triazines has been perfect, as palladocatalyzed CH arylation pathway on imidazo[1,2-b][1,2,4,5]tetrazine. A part is devoted to Groebke-Blackburn multicomponant reaction. Various pharmacological analyses were carried out in particular with inhibition of various kinases and cytotoxicity evaluation on various human cancer cell lines
S, Venkatesan. "Synthesis and inhibition studies of steviamine stereoisomers, novel triazole and tetrazole-fused five membered iminocyclitols". Thesis, 2018. http://eprint.iitd.ac.in:80//handle/2074/7939.
Texto completoRadies, Hendrik [Verfasser]. "Tetrazole und Triazole als neuartige Oxidationsmittel in IR-Täuschkörpern / vorgelegt von Hendrik Radies". 2009. http://d-nb.info/100399329X/34.
Texto completoCapítulos de libros sobre el tema "Triazole and tetrazole"
Naik, Anil D., Antoine P. Railliet, Marinela M. Dîrtu y Yann Garcia. "Coordination preference and magnetic properties of FeII assemblies with a bis-azole bearing 1,2,4-triazole and tetrazole". En ICAME 2011, 119–23. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-4762-3_15.
Texto completoOstrovskii, Vladimir A. y Rostislav E. Trifonov. "Fluorinated Triazoles and Tetrazoles". En Fluorine in Heterocyclic Chemistry Volume 1, 459–513. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04346-3_11.
Texto completoGupta, Pankuri y Abha Sharma. "Pharmacological Significance of Triazoles and Tetrazoles in Neurodegenerative Disease: An Overview". En N-Heterocycles, 355–93. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_10.
Texto completoJadhav, Popat M., A. B. Kanagare, Anand B. Dhirbassi, Atam B. Tekale, R. M. Borade, S. U. Tekale, Keshav Lalit Ameta y R. P. Pawar. "Recent Advances in Nanocatalyzed Synthesis of Triazoles and Tetrazoles and Their Biological Studies". En Nanocatalysis, 177–200. New York: CRC Press, 2022. http://dx.doi.org/10.1201/9781003141488-8.
Texto completoBegtrup, Mikael. "Diazole, Triazole, and Tetrazole N-Oxides". En Advances in Heterocyclic Chemistry Volume 106, 1–109. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-12-396531-8.00001-8.
Texto completoMurumkar, Prashant R. y Rupesh V. Chikhale. "Vicinal Diaryl Triazoles and Tetrazoles". En Vicinal Diaryl Substituted Heterocycles, 191–219. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-08-102237-5.00006-7.
Texto completoElashry, E. S. H. y N. Rashed. "1,2,4-Triazolo- and Tetrazolo[x,y-z]pyrimidines". En Advances in Heterocyclic Chemistry Volume 72, 127–224. Elsevier, 1998. http://dx.doi.org/10.1016/s0065-2725(08)60316-5.
Texto completoGrimshaw, James. "Photochemistry of Aryl Diazonium Salts, Triazoles and Tetrazoles". En CRC Handbookof Organic Photochemistry and Photobiology, Volumes 1 & 2, Second Edition. CRC Press, 2003. http://dx.doi.org/10.1201/9780203495902.ch43.
Texto completo"Photochemistry of Aryl Diazonium Salts, Triazoles and Tetrazoles". En CRC Handbook of Organic Photochemistry and Photobiology, Volumes 1 & 2, 829–46. CRC Press, 2003. http://dx.doi.org/10.1201/9780203495902-49.
Texto completoGonçalves, Raoni Schroeder B. y Leandro Soter de Mariz e Miranda. "Copper catalysis in the synthesis of 1,2,3-triazoles and tetrazoles". En Copper in N-Heterocyclic Chemistry, 75–113. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-821263-9.00003-5.
Texto completoActas de conferencias sobre el tema "Triazole and tetrazole"
Jovanović-Šanta, Suzana S., Aleksandar M. Oklješa, Antos B. Sachanka, Yaraslau U. Dzichenka y Sergei A. Usanov. "17-SUBSTITUTED STEROIDAL TETRAZOLES – NOVEL LIGANDS FOR HUMAN STEROID-CONVERTING CYP ENZYMES". En 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.336js.
Texto completoSzymanowska, Anna, Kamila Buzun, Wojciech Szymanowski, Robert Czarnomysy, Agnieszka Gornowicz, Mariusz Mojzych, Anna Bielawska y Krzysztof Bielawski. "The pro-apoptotic effect of novel pyrazolo[4,3-e]tetrazolo[4,5-b][1,2,4]triazine derivatives in HT-29 colon cancer cells". En RAD Conference. RAD Centre, 2021. http://dx.doi.org/10.21175/rad.abstr.book.2021.8.3.
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