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Relevant bibliographies by topics / Tetrazolona

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Academic literature on the topic 'Tetrazolona'

Author: Grafiati

Published: 5 September 2021

Last updated: 29 July 2025

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Journal articles on the topic "Tetrazolona"

1

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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2

Khidre, Rizk E., Tahah A. Ameen, and Mounir A. I. Salem. "Tetrazoloquinolines: Synthesis, Reactions, and Applications." Current Organic Chemistry 24, no. 4 (2020): 439–64. http://dx.doi.org/10.2174/1385272824666200217095341.

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This review summarizes the synthesis, reactions, and biological activities of tetrazolo[1,5-a]quinoline derivatives. These derivatives were synthesized by several methods such as i) from the reaction of 2-chloroquinoline with sodium azide ii) from diazotization 2-hydrazinylquinoline derivatives, and iii) from intramolecular cyclocondensation of 2-azidoarylidenes. Also, the chemical reactions and pharmacological activities of some tetrazoloquinolines such as tetrazolo[1,5-a]quinoline-4-carbaldehyde, 5-chlorotetrazolo[ 1,5-a]quinoline, 4-(chloromethyl)tetrazolo[1,5-a]quinoline, tetrazolo[1,5- a]

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3

Reason, Thomas E., Benjamin Goka, Jeanette A. Krause, Abelline K. Fionah, Elsayed M. Zahran, and Sundeep Rayat. "Cu2O nanoparticle-catalyzed synthesis of diaryl tetrazolones and investigation of their solid-state properties." CrystEngComm 23, no. 17 (2021): 3220–29. http://dx.doi.org/10.1039/d1ce00119a.

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1,4-Diaryl tetrazolones 1 have been synthesized by Cu<sub>2</sub>O nanoparticle-catalyzed C–N coupling of aryl tetrazolones 2 with aryl boronic acids 3 in the presence of oxygen, and their crystal structures have been reported.

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4

He, Piao, Le Wu, Jin-Ting Wu, Xin Yin, Michael Gozin, and Jian-Guo Zhang. "Alkali and alkaline earth metal salts of tetrazolone: structurally interesting and excellently thermostable." Dalton Transactions 46, no. 26 (2017): 8422–30. http://dx.doi.org/10.1039/c7dt01179b.

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5

Duncton, Matthew A. J., Ryan B. Murray, Gary Park, and Rajinder Singh. "Tetrazolone as an acid bioisostere: application to marketed drugs containing a carboxylic acid." Organic & Biomolecular Chemistry 14, no. 39 (2016): 9343–47. http://dx.doi.org/10.1039/c6ob01646d.

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6

Monzon, Loana I., Nicole C. M. Rocha, Gabriela T. Quadros, et al. "Synthesis of 4-(Phenylchalcogenyl)tetrazolo[1,5-a]quinolines by Bicyclization of 2-Azidobenzaldehydes with Phenylchalcogenylacetonitrile." Molecules 28, no. 13 (2023): 5036. http://dx.doi.org/10.3390/molecules28135036.

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A general methodology to access valuable 4-(phenylchalcogenyl)tetrazolo[1,5-a]quinolines was developed by the reaction of 2-azidobenzaldehyde with phenylchalcogenylacetonitriles (sulfur and selenium) in the presence of potassium carbonate (20 mol%) as a catalyst. The reactions were conducted using a mixture of dimethylsulfoxide and water (7:3) as solvent at 80 °C for 4 h. This new methodology presents a good functional group tolerance to electron-deficient and electron-rich substituents, affording a total of twelve different 4-(phenylchalcogenyl)tetrazolo[1,5-a]quinolines selectively in modera

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7

Könnecke, Andreas, Christian Richter, and Eberhard Lippmann. "s-Triazolo[4,3-c]tetrazolo[1,5-a]pyrimidine aus 5-substituierten Tetrazolen und 5-Chlor-7-methyltetrazolo[1,5-a]py-rimidin." Zeitschrift für Chemie 19, no. 3 (2010): 101–2. http://dx.doi.org/10.1002/zfch.19790190310.

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8

Duncton, Matthew A. J., and Rajinder Singh. "A one-pot synthesis of tetrazolones from acid chlorides: understanding functional group compatibility, and application to the late-stage functionalization of marketed drugs." Organic & Biomolecular Chemistry 14, no. 39 (2016): 9338–42. http://dx.doi.org/10.1039/c6ob01644h.

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9

Sepsey Für, Csilla, György Keglevich, and Hedvig Bölcskei. "Unexpected Formation of 4-aryl-1-(Propane-2-ylidenehydrazono)-2,3-diazaspiro[5.5]undec-3-ene by the Reaction of Pyridazinethiones Derivatives with Hydrazine." Molbank 2021, no. 3 (2021): M1243. http://dx.doi.org/10.3390/m1243.

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After making a new series of spiro[cycloalkane]pyridazinones with high Fsp3 character available, the new target was to synthesize derivatives comprising nitrogen-containing heterocycles, such as triazolo or tetrazolo rings. The corresponding thioxo derivatives (1a,b) seemed to be good starting materials for the synthesis of tetrazolo derivatives. The reaction of the pyridazinethiones (1a,b) with hydrazine surprisingly resulted in Schiff bases (3a,b) deriving from the reaction of hydrazones (2a,b) with acetone.

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10

Ramírez-López, Sandra C., M. V. Basavanag Unnamatla, and Rocío Gámez-Montaño. "Solvent-Free Synthesis of Imidazo [1,2-a] pyridin-tetrazolo [1,5-a] Quinolines via an IMCR One-Pot Process." Proceedings 9, no. 1 (2018): 41. http://dx.doi.org/10.3390/ecsoc-22-05796.

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A solvent-free and catalyst-free synthesis of fused bis-heterocycles containing imidazo[1,2-a]pyridine and tetrazolo[1,5-a]quinoline frameworks is reported via a one-pot process. This Groebke–Blackburn–Bienaymé reaction (GBBR)/SNAr/ring-chain azido tautomerization cascade proceeds under eco-friendly conditions. The tetrazolo[1,5-a]quinoline and imidazo[1,2-a]pyridine scaffolds are present in various compounds with interesting pharmacological properties and could lead to the discovery of novel bioactive molecules.

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Dissertations / Theses on the topic "Tetrazolona"

1

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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2

Oliveira, Lanussy Porfiro de. "Atividade analgésica, anti-inflamatóriae vasorelaxante de dois derivados pirazólicos: 5-[1-(4- fluorfenil)-1H-pirazol-4-IL]-2H-tetrazola(LQFM 020) e 5- [1-(2-fluorofenil)-1H-pirazol-4-IL]-2H-tetrazola (LQFM 039)." Universidade Federal de Goiás, 2014. http://repositorio.bc.ufg.br/tede/handle/tede/4876.

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Submitted by Cláudia Bueno (claudiamoura18@gmail.com) on 2015-11-11T20:45:46Z No. of bitstreams: 2 Dissertação - Lanussy Porfiro de Oliveira - 2014.pdf: 1478536 bytes, checksum: 2646f221282c9b288ef2da403ef374d4 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)<br>Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2015-11-12T09:40:17Z (GMT) No. of bitstreams: 2 Dissertação - Lanussy Porfiro de Oliveira - 2014.pdf: 1478536 bytes, checksum: 2646f221282c9b288ef2da403ef374d4 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b

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Prata, Amílcar Duque. "Fotoquímica de Tetrazolonas: Um Estudo Teórico." Master's thesis, 2020. http://hdl.handle.net/10316/92491.

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Dissertação de Mestrado em Química apresentada à Faculdade de Ciências e Tecnologia<br>Os compostos tetrazólicos apresentam aplicações em áreas que se estendem da Química Medicinal até à indústria de materiais energéticos. As tetrazolonas incluem-se na família de compostos tetrazólicos, e distinguem-se por formarem um grupo carbonilo com o carbono do anel tetrazólico.A fotoquímica destes compostos foca-se na clivagem do anel, apresentando, na maioria dos casos, azidas, isocianatos e aziridinas como produtos finais, estando descritas, no entanto, várias vias reacionais alternativas. Estas vias

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4

Peters, Lars [Verfasser]. "Nichtkovalente Wechselwirkungen von Tetrazolen und Carbonsäuren mit Amidinbasen / vorgelegt von Lars Peters." 2001. http://d-nb.info/961829281/34.

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Books on the topic "Tetrazolona"

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

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

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Book chapters on the topic "Tetrazolona"

1

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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2

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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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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4

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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5

Elashry, E. S. H., and N. Rashed. "1,2,4-Triazolo- and Tetrazolo[x,y-z]pyrimidines." In Advances in Heterocyclic Chemistry Volume 72. Elsevier, 1998. http://dx.doi.org/10.1016/s0065-2725(08)60316-5.

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6

Aggarwal, P., and M. W. P. Bebbington. "Ring Cleavage of Tetrazolo[1,5-][1,2,4]triazin-7-amines." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-117-00281.

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7

"Tetrazolo[5,1-a]phthalazine to Azepino[2,1-b]-1,3-benzothiazole." In Substance Index Cyclic Compounds VIII, Tricyclic compounds II, edited by Büchel, Falbe, Hagemann, et al. Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114893.

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8

"A. Herstellung: 5. aus anderen Tetrazolen unter Erhaltung des Ringsystems (I)." In Hetarene III, edited by Ernst Schaumann. Georg Thieme Verlag, 1994. http://dx.doi.org/10.1055/b-0035-110367.

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9

"A. Herstellung: 5. aus anderen Tetrazolen unter Erhaltung des Ringsystems (II)." In Hetarene III, edited by Ernst Schaumann. Georg Thieme Verlag, 1994. http://dx.doi.org/10.1055/b-0035-110368.

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10

"4H-Benzopyrano[3,4-d]-1,2,5-oxadiazole to 3,5-Dihydro-tetrazolo[5,1-b]quinazoline." In Substance Index Cyclic Compounds VIII, Tricyclic compounds II, edited by Büchel, Falbe, Hagemann, et al. Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114892.

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Conference papers on the topic "Tetrazolona"

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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Reports on the topic "Tetrazolona"

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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