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Relevant bibliographies by topics / Tetrazolo

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Academic literature on the topic 'Tetrazolo'

Author: Grafiati

Published: 4 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Tetrazolo"

1

Ramírez-López, Sandra C., M. V. Basavanag Unnamatla, and Rocío Gámez-Montaño. "A One-Pot Process for the Synthesis of Alkyne-3-tretrazolyl-tetrazolo [1,5-a] Quinolines." Proceedings 9, no. 1 (2018): 42. http://dx.doi.org/10.3390/ecsoc-22-05798.

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An efficient synthesis of alkyne-3-tetrazolyl-tetrazolo[1,5-a] quinolones via a one-pot isocyanide-based multicomponent reaction (IMCR) process: I-MCR Ugi-azide/SNAr/ring-chain azido tautomerization was performed under eco-friendly conditions. We report the one-pot synthesis of tris-heterocycles containing a tetrazolo[1,5-a] quinoline connected to a 1,5-disubstituted-tetrazole (1,5-DS-T). The synthesis of these compounds is of great interest in synthetic and medicinal chemistry because these heterocycles are considered privileged scaffolds and their preparation and evaluation may lead to the d

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2

Liu, Teng, Yi-Gang Ji, and Lei Wu. "tert-Butyl nitrite-mediated radical cyclization of tetrazole amines and alkynes toward tetrazolo[1,5-a]quinolines." Organic & Biomolecular Chemistry 17, no. 10 (2019): 2619–23. http://dx.doi.org/10.1039/c9ob00169g.

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He, Piao, Jian-Guo Zhang, Kun Wang, Xin Yin, Shao-Wen Zhang, and Jian-She Jiao. "Calculations predict a novel desired compound containing eight catenated nitrogen atoms: 1-amino-tetrazolo-[4,5-b]tetrazole." RSC Adv. 4, no. 48 (2014): 25302–9. http://dx.doi.org/10.1039/c4ra03515a.

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4

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.

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In this study, two insensitive energetic compounds using fused triazolo-triazine and tetrazolo-triazine as the framework, one amino and one tetrazole as functional groups, were prepared through a two-step reaction.

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Madhavachary, Rudrakshula, Qian Wang, and Alexander Dömling. "With unprotected amino acids to tetrazolo peptidomimetics." Chemical Communications 53, no. 61 (2017): 8549–52. http://dx.doi.org/10.1039/c7cc03370b.

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We have synthesized a library of tetrazolo peptidomimetics in two steps. The universality of this Ugi-tetrazole reaction was further examined using the N,C-unprotected dipeptide Gly–Gly and tripeptide Gly–Gly–Gly for the first time.

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Suresh, Lingala, P. Sagar Vijay Kumar, T. Vinodkumar, and 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, no. 73 (2016): 68788–97. http://dx.doi.org/10.1039/c6ra16307f.

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A ceria nanocatalyst was used for the one-pot, multicomponent condensation reaction of benzoylacetonitrile, aromatic aldehydes and 5-amino-triazole/tetrazole proceeding via C–C and C–N bond formation to deliver triazolo/tetrazolo[1,5-a]pyrimidines.

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Scapin, Elisandra, Paulo R. S. Salbego, Caroline R. Bender, et al. "Synthesis, effect of substituents on the regiochemistry and equilibrium studies of tetrazolo[1,5-a]pyrimidine/2-azidopyrimidines." Beilstein Journal of Organic Chemistry 13 (November 10, 2017): 2396–407. http://dx.doi.org/10.3762/bjoc.13.237.

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An efficient synthesis methodology for a series of tetrazolo[1,5-a]pyrimidines substituted at the 5- and 7-positions from the cyclocondensation reaction [CCC + NCN] was developed. The NCN corresponds to 5-aminotetrazole and CCC to β-enaminone. Two distinct products were observed in accordance with the β-enaminone substituent. When observed in solution, the compounds can be divided into two groups: (a) precursor compounds with R = CF3 or CCl3, which leads to tetrazolo[1,5-a]pyrimidines in high regioselectivity with R at the 7-position of the heterocyclic ring; and (b) precursor compounds with R

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Leškovskis, Kristaps, Anatoly Mishnev, Irina Novosjolova, and Māris Turks. "SNAr Reactions of 2,4-Diazidopyrido[3,2-d]pyrimidine and Azide-Tetrazole Equilibrium Studies of the Obtained 5-Substituted Tetrazolo[1,5-a]pyrido[2,3-e]pyrimidines." Molecules 27, no. 22 (2022): 7675. http://dx.doi.org/10.3390/molecules27227675.

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A straightforward method for the synthesis of 5-substituted tetrazolo[1,5-a]pyrido[2,3-e]pyrimidines from 2,4-diazidopyrido[3,2-d]pyrimidine in SNAr reactions with N-, O-, and S- nucleophiles has been developed. The various N- and S-substituted products were obtained with yields from 47% to 98%, but the substitution with O-nucleophiles gave lower yields (20–32%). Furthermore, the fused tetrazolo[1,5-a]pyrimidine derivatives can be regarded as 2-azidopyrimidines and functionalized in copper(I)-catalyzed azide-alkyne dipolar cycloaddition (CuAAC) and Staudinger reactions due to the presence of a

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9

Mamdouh, A. M. Taha. "Use of 1,5-diaminotetrazole in the synthesis of some fused heterocyclic compounds." Journal of Indian Chemical Society Vol. 82, Feb 2005 (2005): 172–74. https://doi.org/10.5281/zenodo.5825077.

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Department of Chemistry, Faculty of Science, Cairo University at Faiyoum, Egypt <em>Manuscript received 5 May 2004, accepted 2 September 2004</em> 1,5-Diaminotetrazole was reacted in 'one-pot' with one carbon cyclizing reagents to afford the corresponding 1,2,4-triazolo[1,5- d]tetrazoles. Analogues reactions with nitrous acid, benzil, diethyl oxalate, pyruvic acid and ethyl acetoacetate afforded tetrazolo-heterocycles for biological interest. 

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Bonyad, Ali Moin. "Synthesis of Chalcones from Acetone and tetrazole and 2-acetyl naphthalene Assisted by Microwave." Engineering and Technology Quarterly Reviews 3, no. 1 (2020): 16–22. https://doi.org/10.5281/zenodo.3686827.

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In the present study, we understood the total synthesis one chalcone derivative via Claisen-Schmidt condensation of the respective aldehydes and ketones using Microwave assisted irradiation method. In the microwave environment, chemical reactions usually proceed faster and give higher yields with fewer by- products. In the synthesis, a common aldehyde namely tetrazolo {1, 5-a} quinoline-4-carbaldehyde was used while the ketones used were respectively acetone, 2- acetyl Naphthalene. The Chalcone synthesised from Tetrazolo {1, 5-a} quinolone-4-carbaldehyde and acetone was 4-(tetrazolo {1, 5-a} q

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Dissertations / Theses on the topic "Tetrazolo"

1

Krest, Alexander [Verfasser]. "Synthese neuer Tetrazole, N-Alkyltetrazole und Übergangsmetall(II)komplexe mit Tetrazolat-Liganden / Alexander Krest." München : Verlag Dr. Hut, 2015. http://d-nb.info/1080754164/34.

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Costa, Thiago Santangelo. "Obtenção do copolímero de acrilonitrila e vinil-tetrazol e sua aplicação como inibidor de corrosão para meio ácido." Universidade do Estado do Rio de Janeiro, 2007. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=2803.

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Polímeros heterocíclicos abrangem uma grande variedade de materiais, desde simples polímeros lineares sintetizados a partir de monômeros do tipo heterocíclicos vinílicos até polímeros altamente funcionalizados e reticulados. Neste trabalho realizou-se a modificação química da poliacrilonitrila com a incorporação de grupos tetrazol em diferentes teores (1%, 2,5%, 5% e 10%). Os copolímeros de acrilonitrila e vinil-tetrazol obtidos foram caracterizados por FTIR e o seu comportamento térmico analisado por DSC e TGA. Os polímeros heterocíclicos foram avaliados como inibidores de corrosão para aço-c

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Cloarec, Thomas. "Processing and Characterization of Polycarbonate Foams with Supercritical Co2 and 5-Phenyl-1H-tetrazole." Thesis, University of North Texas, 2015. https://digital.library.unt.edu/ark:/67531/metadc799500/.

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Since their discovery in the 1930s, polymeric foams have been widely used in the industry for a variety of applications such as acoustical and thermal insulation, filters, absorbents etc. The reason for this ascending trend can be attributed to factors such as cost, ease of processing and a high strength to weight ratio compared to non-foamed polymers. The purpose of this project was to develop an “indestructible” material made of polycarbonate (PC) for industrial applications. Due to the high price of polycarbonate, two foaming methods were investigated to reduce the amount of material used.

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Cezário, Wendel Rodrigues. "Avaliação do copolímero de acrilonitrila e 5-vinil-tetrazol na eficiência de inibição de corrosão química." Universidade do Estado do Rio de Janeiro, 2010. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=2141.

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A corrosão é um processo resultante da ação do meio sobre um determinado material, causando sua deterioração. Em geral, essa deterioração causa prejuízos incalculáveis, fazendo com que o material se torne inadequado ao uso. Os heterocíclicos apresentam inúmeras aplicações tecnológicas e em alguns casos médico-farmacológicas. Mais recentemente, esses compostos têm sido utilizados como eficientes inibidores de corrosão para a proteção de metais em meio ácido ou salino. Nesta Dissertação realizou-se a modificação química da poliacrilonitrila com a incorporação de grupos tetrazol em diferentes teo

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Oliveira, Edson de Almeida Ferreira. "Modificação química da poliacrilonitrila com grupos tetrazol assistida por micro-ondas." Universidade do Estado do Rio de Janeiro, 2011. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=2609.

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Nos últimos anos, a irradiação por micro-ondas tem sido cada vez mais usada na síntese de varias moléculas orgânicas, devido a uma série de vantagens que essa nova tecnologia apresenta. Até o momento, existem poucos estudos sobre polimerizações assistidas por micro-ondas e menos ainda sobre a modificação de polímeros usando essa nova fonte de energia. Polímeros heterocíclicos contendo anéis azóicos, como o tetrazol possuem interesse acadêmico e comercial devido as suas várias aplicações. Nesta Dissertação foi estuda a modificação química da poliacrilonitrila pela incorporação em sua cadeia pol

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6

Castro, Guilherme Vieira de. "Síntese de tetrazóis a partir de cianamidas : novos ligantes do receptor PPARy." reponame:Repositório Institucional da UFABC, 2014.

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Orientadora: Prof.ª Dr.ª Mirela Inês de Sairre<br>Dissertação (mestrado) - Universidade Federal do ABC, Programa de Pós-Graduação em Ciência & Tecnologia - Química, 2014.<br>Dentro da superfamilia de proteinas chamadas de receptores nucleares, tem-se como um importante alvo terapeutico o receptor PPAR¿Á, uma proteina que participa de muitos processos de regulacao do metabolismo de lipideos e carboidratos, fazendo com que a modulacao deste receptor seja uma alternativa de grande importancia para o tratamento de diversas doencas como a sindrome metabolica, diabetes melito tipo 2 e a obesidade. N

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Bhandari, Sonali. "Organometallic tetrazoles." Thesis, University of Bath, 1998. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390309.

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8

Samanta, Susnata. "Reversible carbon dioxide gels, synthesis and characterization of energetic ionic liquids, synthesis and characterization of tetrazole monomers and polymers, encapsulation of sodium azide for controlled release." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2007. http://hdl.handle.net/1853/22602.

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Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2007.<br>Committee Chair: Prof. Charles L. Liotta; Committee Member: Prof. Arthur J. Ragauskas; Committee Member: Prof. Charles A. Eckert; Committee Member: Prof. John D. Muzzy; Committee Member: Prof. Rigiberto Hernandez.

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Peters, Lars. "Nichtkovalente Wechselwirkungen von Tetrazolen und Carbonsäuren mit Amidinbasen." [S.l. : s.n.], 2001. http://deposit.ddb.de/cgi-bin/dokserv?idn=961829281.

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10

Young, Richard Getliff. "Tetrazoles in heterocyclic synthesis." Thesis, Imperial College London, 1989. http://hdl.handle.net/10044/1/47727.

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Books on the topic "Tetrazolo"

1

Prokudin, V. G. O termicheskom razlozhenii tetrazola i 5-zameshchennykh tetrazolov. Otd-nie In-ta khim. fiziki AN SSSR, 1989.

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2

Poganiuch, Peter. Untersuchung des thermisch- und lichtinduzierten Spinüberganges in Eisen(II)-Komplexen [Eisen-Komplexen] des Typs [Fe(1-Methyl-1H-tetrazol)₆]X₂ [Fe-Methyl-H-tetrazol-X]: (X = BF⁻₄, ClO⁻₄, PF⁻₆, CF₃SO⁻₃). [s.n.], 1989.

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3

Gutenberg-Universität, Johannes, ed. Untersuchungen zum thermischen und lichtinduzierten Spinübergang in Eisen(II)-Komplexen mit Triazol- und Tetrazol-Liganden. [s.n.], 1996.

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4

Brehme, Franziska. Oxime und 1H-Tetrazol-ole als NO-Donatoren. 1997.

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Prokudin, V. G. O mekhanizme monomolekuli͡arnogo termicheskogo razlozhenii͡a 1,5- i 2,5-dizameshchennykh tetrazolov: Preprint. 1989.

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6

Izuchenie mitokhondriĭ i bakteriĭ s pomoshchʹi͡u soli tetrazolii͡a p-NTF. Akademii͡a nauk SSSR, Nauch. t͡sentr biologicheskikh issledovaniĭ, In-t biologicheskoĭ fiziki, 1990.

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7

Singh, Rajesh Kumar, ed. Key Heterocyclic Cores for Smart Anticancer Drug–Design Part I. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150400741220101.

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This book provides an update on heterocyclic compounds that serve as key components of anti-cancer agents administered in pre-clinical settings. Many of the compounds highlighted in the book are being actively investigated for the bioactive properties against a range of cancer cell lines. There is potential for heterocyclic compounds to design agents that can target specific molecules to treat different types of cancers. Chapters are contributed by experts in pharmaceutical chemistry and are written to give a general overview of the topic to readers involved in all levels of research and decis

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Book chapters on the topic "Tetrazolo"

1

Sherazi, Tauqir A. "Tetrazole Group." In Encyclopedia of Membranes. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_575-1.

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Sherazi, Tauqir A. "Tetrazole Group." In Encyclopedia of Membranes. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_575.

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3

Dreikorn, Barry A., and Gregory L. Durst. "Retrospective Quantitative Structure—Activity Relationship (QSAR) Analysis of Tetrazolo- and Triazoloquinolines, a Series of Rice Blast Control Agents." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0584.ch031.

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Matyáš, Robert, and Jiří Pachman. "Tetrazoles." In Primary Explosives. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-28436-6_8.

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Lieber, Eugene, Taskashi Enkoji, and Raymond C. Burrows. "Tetrazolone." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132371.ch18.

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Matyáš, Robert, and Jiří Pachman. "Tetrazole Ring-Containing Complexes." In Primary Explosives. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-28436-6_9.

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7

Klapötke, Thomas M., and Jörg Stierstorfer. "Energetic TetrazoleN-oxides." In Green Energetic Materials. John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118676448.ch06.

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8

Ellis, G. P. "Chromone Carbonitriles and Tetrazole Derivatives." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187012.ch18.

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Banupriya, K., and B. Preethi. "Synthesis, Anticancer Evaluation, and Molecular Docking Studies of Novel 1-Phenyl-3A,9-Dihydro-1H-Benzo[E]Tetrazolo[5,1-b][1,3]Thiazine with the Inhibitor." In Springer Proceedings in Physics. Springer Nature Switzerland, 2024. https://doi.org/10.1007/978-3-031-69970-2_22.

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10

Ostrovskii, Vladimir A., and Rostislav E. Trifonov. "Fluorinated Triazoles and Tetrazoles." In Fluorine in Heterocyclic Chemistry Volume 1. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04346-3_11.

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Conference papers on the topic "Tetrazolo"

1

Hu, Anguang, Fan Zhang, Mark Elert, et al. "AB INITIO MOLECULAR DYNAMICS SIMULATIONS ON SENSITIVITY OF NITROGEN-RICH POLY-TETRAZOLO ENERGETIC COMPOUNDS." In SHOCK COMPRESSION OF CONDENSED MATTER 2009: Proceedings of the American Physical Society Topical Group on Shock Compression of Condensed Matter. AIP, 2009. http://dx.doi.org/10.1063/1.3295265.

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2

Scapin, Elisandra, Lilian Buriol, Clarissa Piccinin Frizzo, and Marcos A. P. Martins. "Synthesis of 7-trifluo[trichlo]romethyl-5-aryl[alkyl]-tetrazolo[1,5-a] pyrimidines in Ionic Liquid." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819155310.

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3

Szymanowska, Anna, Kamila Buzun, Wojciech Szymanowski, et al. "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." In RAD Conference. RAD Centre, 2021. http://dx.doi.org/10.21175/rad.abstr.book.2021.8.3.

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Nurminen, Erkki J., Jorma K. Mattinen, and Harri Lönnberg. "Catalysis in tetrazole-promoted phosphoramidite alcoholysis." In XIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902219.

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Samal, Kanyanjali, Manini Nayak, and Anita Pati. "Microwave assisted synthesis of tetrazole derivative." In 2ND INTERNATIONAL CONFERENCE ON EMERGING SMART MATERIALS IN APPLIED CHEMISTRY (ESMAC-2021): ESMAC-2021. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0127508.

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Helmy, A., and W. Tong. "Thermal decomposition of 5 amino tetrazole propellant." In 36th AIAA/ASME/SAE/ASEE Joint Propulsion Conference and Exhibit. American Institute of Aeronautics and Astronautics, 2000. http://dx.doi.org/10.2514/6.2000-3330.

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Rogozin, Mark, Konstantin Pekhotin, Oksana Golubtsova, Rudolf Stepanov, Ludmila Kruglyakova, and Alexander Vasiliev. "Synthesis of 2-nitromethyl-5-nitro-1,2,3,4-tetrazole." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01877.

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Natale Domingos Tamacia Giraldelo, Denise, and Gisele Herbst Vazquez. "RELAÇÃO ENTRE A CONDUTIVIDADE ELÉTRICA E O DESEMPENHO DE SEMENTES DE UROCHLOA BRIZANTHA EM CAMPO." In ANAIS V CONTEC BRASIL 2024. Universidade Brasil, 2024. https://doi.org/10.63021/vcontec.978-6589249313.2024.art039.

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Introdução: O Brasil é o maior produtor, consumidor e exportador de sementes de poáceas forrageiras do mundo. A determinação da condutividade elétrica (CE) é um dos testes mais rápidos na avaliação da qualidade e vigor de sementes, contudo, os estudos para espécies forrageiras são escassos. Objetivos: Correlacionar os resultados do teste de CE com os de emergência e de tetrazólio em sementes de Urochloa brizantha, de forma a determinar valores que indiquem a qualidade de um lote e se este é ou não apropriado para a semeadura. Material e Métodos: O experimento está sendo conduzido na Universida

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Gudkova, Inessa, and David Lempert. "SOME HYPOTETICAL TETRAZOLE DERIVATIVES AS COMPONENTS OF SOLID COMPOSITE PROPELLANTS." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m763.aks-2019/241-245.

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Kabanov, D. S., M. P. Kitaeva, and T. A. Fedotcheva. "YELLOW TETRAZOLE FOR CYTOTOXIC ASSAY OF PLANT BIOLOGICALLY ACTIVE SUBSTANCES." In 90 лет - от растения до лекарственного препарата: достижения и перспективы. Федеральное государственное бюджетное научное учреждение "Всероссийский научно-исследовательский институт лекарственных и ароматических растений", 2021. http://dx.doi.org/10.52101/9785870191003_2021_607.

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Reports on the topic "Tetrazolo"

1

Lowe-Ma, Charlotte K., Robin A. Nissan, and William S. Wilson. Tetrazolo(1,5-A)pyridines and Furazano(4,5-B)pyridine-1-oxides as Energetic Materials. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada209357.

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