Relevant bibliographies by topics / Oxadiazol

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Oxadiazol'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Oxadiazol"

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Solet, Sanwar Mal, Neetesh Kumar Sharma, and Raghvendra Singh Bhadauria. "Synthesis of 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives." Journal of Drug Delivery and Therapeutics 9, no. 4-A (2019): 528–60. http://dx.doi.org/10.22270/jddt.v9i4-a.3514.

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Synthesis of a series of various 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives (7a-7u) have been done. Synthesis of a series of intermediates (3a-3c and 5a-5c) have been also done, ethyl-2-phenoxyacetate (3a), ethyl 2-(2, 4-dichlorophenoxy)acetate (3b), ethyl 2-(4-nitrorophenoxy) acetate (3c), 2-phenoxyacetohydrazide (5a), 2-(2, 4-dichlorophenoxy) acetohydrazide (5b), 2-(4-nitrophenoxy)acetohydrazide (5c), and final product (7a-7u), 2-(phenoxymethyl)-5-phenyl-1, 3, 4-oxadiazole (7a), 4-(5-(phenoxymethyl)-1, 3, 4-oxadiazol-2-yl)aniline (7b), 3-(5-(phenoxymethyl)-1, 3, 4-oxadiazol-2-yl) anil
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Solet, Sanwar Mal, Neetesh Kumar Sharma, and Raghvendra Singh Bhadauria. "Biological Evaluation of Novel Synthesized 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives." Journal of Drug Delivery and Therapeutics 9, no. 4-A (2019): 573–76. http://dx.doi.org/10.22270/jddt.v9i4-a.3522.

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Synthesis of a series of various 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives (7a-7v) have been done previously. These novel synthesized derivatives (7a-7v) have been tested for their antibacterial activity against Gram +ve S. aureus and Gram -ve E. Coli bacterias by broth dilution method. A comparative study has been done for all derivatives. Based on the visual turbidity, the MIC of the evaluated molecules has been studied, the evaluation concentration was used single therefore, the exact MIC could not determined and results are represented in less than and more than based on growth of
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Górecki, Sebastian, and Agnieszka Kudelko. "Synthesis and Characterization of Novel 2-Alkyl-1,3,4-Oxadiazoles Containing a Phenylazo Group." Molecules 29, no. 18 (2024): 4316. http://dx.doi.org/10.3390/molecules29184316.

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An efficient method for the synthesis of novel phenylazo-containing moieties is described. The derivatives of 5-(4-(phenyldiazenyl)phenyl)-1,3,4-oxadiazole, substituted at position 2 of the heterocyclic scaffold with alkyl groups of different chain lengths, were prepared. The titled compounds were obtained using the appropriate 4-(5-alkyl-1,3,4-oxadiazol-2-yl)anilines, which were directed to diazotization and subsequently coupled to phenol, resorcinol, and N,N-dimethylaniline. Additionally, we report a mild and effective procedure for the preparation of 4-(5-alkyl-1,3,4-oxadiazol-2-yl)anilines
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Tang, Yongxing, Chunlin He, Lauren A. Mitchell, Damon A. Parrish, and Jean'ne M. Shreeve. "Energetic compounds consisting of 1,2,5- and 1,3,4-oxadiazole rings." Journal of Materials Chemistry A 3, no. 46 (2015): 23143–48. http://dx.doi.org/10.1039/c5ta06898c.

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3-Nitroamino-4-(5-amino-1,3,4-oxadiazol-2-yl)furazan monohydrate (2·H<sub>2</sub>O), which is a combination of the nitroaminofurazan and 1,3,4-oxadiazole rings, was obtained by the nitration of 3-amino-4-(5-amino-1,3,4-oxadiazol-2-yl)furazan (1) with 100% nitric acid.
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Stepanova, Elena V., and Andrei I. Stepanov. "UNUSUAL WAY OF REACTION OF 3-AMINO-4-(5-CHLOROMETHYL-1,2,4-OXADIAZOLE-3-YL)-FURAZAN WITH HYDRAZINE." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 60, no. 4 (2017): 26. http://dx.doi.org/10.6060/tcct.2017604.5522.

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The results of our study of the pathways of selective reactivity of 3-amino-4-(5-chloromethyl-1,2,4-oxadiazole-3-yl)furazan versus 5-unsubstituted or 5-methyl and 5-trifluoromethyl substituted 4-(5R-1,2,4-oxadiazole-3-yl)furazans (R = H, Me, CF3) towards the action of hydrazine are discussed. If the reductive opening of 1,2,4-oxadiazole ring in unsubstituted at the С-5 atom (1,2,4-oxadiazol-3-yl)furazan derivatives under the treatment with hydrazine can be used as a method for the preparation of a range of amidrazones of 4-R-furazan-3-carboxylic acid. 3-amino-4-(5-trifluoromethyl-1,2,4-oxadiaz
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Ahsan, Mohamed Jawed, Mohd Zaheen Hassan, Surender Singh Jadav, et al. "Synthesis and Biological Potentials of 5-aryl-N-[4-(trifluoromethyl) phenyl]-1,3,4-oxadiazol-2-amines." Letters in Organic Chemistry 17, no. 2 (2020): 133–40. http://dx.doi.org/10.2174/1570178616666190401193928.

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Oxadiazoles are an important class of heterocyclic compounds, having broad-spectrum activity. They were also reported as anticancer, and antioxidant agents, hence it is of significant importance to explore new oxadiazoles. A series of eleven (5-aryl-N-[4-(trifluoromethyl)phenyl]-1,3,4- oxadiazol-2-amines (6a-k) was synthesized based on the structures of reported compounds, SU-101, IMC38525, and FTAB. All these oxadiazoles were synthesized, characterized by spectral data, and further tested against melanoma, leukemia, colon, lung, CNS, ovarian, renal, breast and prostate cancer cell lines’ pane
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Saini, Sachin. "Synthesis and Anticonvulsant Studies of Thiazolidinone and Azetidinone Derivatives from Indole Moiety." Drug Research 69, no. 08 (2018): 445–50. http://dx.doi.org/10.1055/a-0809-5098.

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Abstract2-Amino-5-(3’-indolomethylene)-1, 3 , 4 - oxadiazole (3) undergoes facile condensation with various aromatic aldehydes to gave 2-substitiuted arylidenylamino-5-(3’- indolomethylene) – 1, 3 , 4 – oxadiazole (4–8). Cyclocondensation of (4–8) with thioglycolic acid and triethylamine yielded 3-[5’-(3”- indolomethylene)- 1’, 3’, 4’- oxadiazol-2’-yl]- 2- (substituted aryl)-4- thiazolidinones (9–13) and 1-[5’-(3”- indolomethylene) -1’, 3’, 4’- oxadiazol - 2’- yl ] -4-(substituted aryl) -2- azetidinones (14–18). The structures of these compounds were established on the basis of analytical and
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R., K. TEWARI, K. MISHRA R., K. SRIVASTAVA SHISHIR, and C. BAHEL S. "Synthesis of some New Mannich Bases, Sulphides and Disulphides of 1,3,4-Oxadiazol-2-thiones as Potential Antifungal Agents." Journal of Indian Chemical Society Vol. 68, Feb 1991 (1991): 108–10. https://doi.org/10.5281/zenodo.6135048.

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Department of Chemistry, University of Gorakhpur, Gorakhpur-273 009 <em>Manuscript&nbsp;received 27 March 1990, revised 14 November 1990, accepted 6 December&nbsp;1990</em> VARIOUS 3, 5-disubstituted-1, 3,4-oxadiazol-2-thiones and several benzidine derivatives display biological activities<sup>1-2</sup>.&nbsp;Several oxadiazolyl sulphides and disulphides also exhibit biological activity<sup>3</sup>.&nbsp;In view of these observations the title compounds, viz. the sulphides, disulphides, benzidine and piperazine derivatives and Mannich bases of substituted-1,3,4- oxadiazoi-2-thiones have been p
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Maftei, Catalin V., Elena Fodor, Peter G. Jones, et al. "Synthesis and characterization of novel bioactive 1,2,4-oxadiazole natural product analogs bearing the N-phenylmaleimide and N-phenylsuccinimide moieties." Beilstein Journal of Organic Chemistry 9 (October 25, 2013): 2202–15. http://dx.doi.org/10.3762/bjoc.9.259.

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Taking into consideration the biological activity of the only natural products containing a 1,2,4-oxadiazole ring in their structure (quisqualic acid and phidianidines A and B), the natural product analogs 1-(4-(3-tert-butyl-1,2,4-oxadiazol-5-yl)phenyl)pyrrolidine-2,5-dione (4) and 1-(4-(3-tert-butyl-1,2,4-oxadiazol-5-yl)phenyl)-1H-pyrrole-2,5-dione (7) were synthesized starting from 4-(3-tert-butyl-1,2,4-oxadiazol-5-yl)aniline (1) in two steps by isolating the intermediates 4-(4-(3-tert-butyl-1,2,4-oxadiazol-5-yl)phenylamino)-4-oxobutanoic acid (3) and (Z)-4-(4-(3-tert-butyl-1,2,4-oxadiazol-5
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Obruchnikova, Natalia V., and Oleg A. Rakitin. "4-(2,5-Dimethyl-1H-pyrrol-1-yl)-1,2,5-oxadiazol-3-amine." Molbank 2023, no. 3 (2023): M1700. http://dx.doi.org/10.3390/m1700.

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1,2,5-Oxadiazol-3-amines with a heterocyclic substituent in the 4-position are being intensively investigated as compounds with valuable pharmacological activity. In this communication, the reaction of 1,2,5-oxadiazole-3,4-diamine with 2,5-hexanedione was shown to selectively give 4-(2,5-dimethyl-1H-pyrrol-1-yl)-1,2,5-oxadiazol-3-amine as a product of the Paal–Knorr reaction. The structure of the synthesized compound was established by elemental analysis, high-resolution mass spectrometry, 1H and 13C NMR, and IR spectroscopy.
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Dissertations / Theses on the topic "Oxadiazol"

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Girotto, Edivandro. "Síntese e caracterização de novos materiais funcionais contendo 1,2,4-oxadiazol, 1,3,4-oxadiazol e 1,2,3-triazol." reponame:Repositório Institucional da UFSC, 2014. https://repositorio.ufsc.br/xmlui/handle/123456789/129283.

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Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas, Programa de Pós-Graduação em Química, Florianópolis, 2014<br>Made available in DSpace on 2015-02-05T20:54:31Z (GMT). No. of bitstreams: 1 327229.pdf: 6986040 bytes, checksum: ce35ce41826360330498fe96fde765a8 (MD5) Previous issue date: 2014<br>Neste trabalho de tese de doutorado são apresentadas as sínteses ecaracterizações de três novas séries dos compostos derivados dosheterociclos 1,2,4-oxadiazol, 1,3,4-oxadiazol e 1,2,3-triazol. Aspropriedades térmicas desses materiais foram investigadas p
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Ferreira, Marli. "Síntese de moléculas com estrutura curvada derivadas dos heterociclos 1,2,4-oxadiazol e 1,3,4-oxadiazol capazes de apresentar mesomofismo." reponame:Repositório Institucional da UFSC, 2012. http://repositorio.ufsc.br/xmlui/handle/123456789/95675.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas, Programa de Pós-Graduação em Química, Florianópolis, 2011<br>Made available in DSpace on 2012-10-26T04:47:00Z (GMT). No. of bitstreams: 1 296869.pdf: 4811314 bytes, checksum: d95c74392d82fee3febbcbb2fd6873c8 (MD5)<br>Neste estudo, a síntese, caracterização e propriedades mesomórficas de dezenove novas moléculas, com estrutura curvada contendo duas unidades de 1,2,4-oxadiazol ou 1,3,4-oxadiazol, são relatadas. A fim de compreender a relação entre a estrutura molecular e o comportamento mes
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Madaram, Karunakar Reddy. "ROUTES TO 1,3,4 – OXADIAZOL-2(3H)-ONES." Wright State University / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=wright1464279310.

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Cristiano, Rodrigo. "Síntese de cristais líquidos fotoluminescentes derivados do heterociclo 1,3,4-Oxadiazol." Florianópolis, SC, 2004. http://repositorio.ufsc.br/xmlui/handle/123456789/86805.

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Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemática. Programa de Pós-Graduação em Química<br>Made available in DSpace on 2012-10-21T10:48:22Z (GMT). No. of bitstreams: 1 203290.pdf: 2061073 bytes, checksum: e006f27b24bf853cd3a3ec78a709c18a (MD5)<br>A síntese, propriedades fotofísicas e térmicas de duas séries de compostos líquido cristalinos fotoluminescentes contendo o heterociclo 1,3,4-oxadiazol são descritas. A primeira série de moléculas constitui-se de 1,3-Bis-[5-(4-alquoxifenil)-1,3,4-oxadiazol-2-il]benzeno (dupla simetria) e 1,3,5-Tri
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Westphal, Eduard. "Síntese de cristais líquidos funcionalizados contendo o heterociclo 1,3,4-oxadiazol." reponame:Repositório Institucional da UFSC, 2013. https://repositorio.ufsc.br/handle/123456789/106888.

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Tese (doutorado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas, Programa de Pós-Graduação em Química, Florianópolis, 2013.<br>Made available in DSpace on 2013-12-05T22:39:25Z (GMT). No. of bitstreams: 1 317574.pdf: 31127469 bytes, checksum: feceea55300609babc7009401b10dd73 (MD5)<br>Neste trabalho são descritas a síntese, a caracterização e os estudos das propriedades ópticas, térmicas, elétricas e organizacionais de novos materiais líquido-cristalinos funcionalizados e derivados do heterociclo 1,3,4-oxadiazol 2,5-dissubstituído. Quatro projetos foram desenv
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Reis, Milena Ramos. "Participação dos canais para potássio nos efeitos cardiovasculares induzidos por um novo composto 1,3,4- oxadiazol." Universidade Federal da Paraí­ba, 2012. http://tede.biblioteca.ufpb.br:8080/handle/tede/6744.

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Made available in DSpace on 2015-05-14T12:59:39Z (GMT). No. of bitstreams: 1 Arquivototal.pdf: 1442527 bytes, checksum: 9d12b86569a24dac4080acc552110564 (MD5) Previous issue date: 2012-02-16<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>It was observed the pharmacological effects of OXDINH, a 1,3,4-oxadiazole derivative obtained by organic synthesis, on the cardiovascular system and the involvement of K+ channels in this response, were studied in rats using techniques combined in vivo and in vitro. In the superior mesenteric artery rings isolated from rats with
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Coelho, Rafael Levi, Ieda Maria 1965 Begnini, and Universidade Regional de Blumenau Programa de Pós-Graduação em Química. "Amidas e ésteres derivados de 1,2,4-oxadiazol com características líquido cristalinas /." reponame:Biblioteca Digital de Teses e Dissertações FURB, 2011. http://www.bc.furb.br/docs/DS/2011/350123_1_1.PDF.

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Tumey, Jonathan Michael. "Synthesis and Reactivity of Sydnone Derived 1,3,4-Oxadiazol-2(3H)-ones." Wright State University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=wright1515170202954677.

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Santos, Alexsandro Fernandes dos. "Síntese, Caracterização e Avaliação Antimicrobiana de Novos Derivados do Sistema 1,3,4-oxadiazol." Universidade Federal da Paraíba, 2015. http://tede.biblioteca.ufpb.br:8080/handle/tede/9010.

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Submitted by Maike Costa (maiksebas@gmail.com) on 2017-06-21T12:11:13Z No. of bitstreams: 1 arquivototal.pdf: 5280829 bytes, checksum: 081debefa3f10398a1c9461855ba5b9d (MD5)<br>Made available in DSpace on 2017-06-21T12:11:14Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 5280829 bytes, checksum: 081debefa3f10398a1c9461855ba5b9d (MD5) Previous issue date: 2015-07-29<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>Two series based on the structure of 2,5-diaryl-1,3,4-oxadiazole were synthesized, 2-aryl-5-methyl-1,3,4-oxadiazole (1a,h) and 2-aryl-5- trifluorometh
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Oliveira, Cledualdo Soares de. "Síntese, caracterização e atividade antimicrobiana de compostos heterocíclicos da classe 2,3-diidro-1,3,4-oxadiazol derivados de N-acilhidrazonas." Universidade Federal da Paraí­ba, 2013. http://tede.biblioteca.ufpb.br:8080/handle/tede/7108.

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Made available in DSpace on 2015-05-14T13:21:26Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 8587505 bytes, checksum: 3dc99b05c6b4e46c71e2ec550261f7cf (MD5) Previous issue date: 2013-01-18<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>Among the heterocyclic compounds, 1,3,4-oxadiazole represents an important unit for the development of new drugs, since compounds containing this unit present a broad spectrum of biological activities such as antibacterial, antifungal, analgesic, anti- inflammatory, antiviral, antitumor, antihypertensive, anticonvulsant, etc.
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Books on the topic "Oxadiazol"

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Tremblay, Rose-Marie. Synthesis of 5-methyl-1, 3, 4-oxadiazol-2-carboxylate esters. Laurentian University, 1994.

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Rakaric, Peter. Oligo - 1, 3, 4 - oxadiazoles. Laurentian University, 1998.

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Ben, Robert N. Synthesis of 2-carboxyethyl-5-methyl-1,3,4-oxadiazole and thiadiazole. Laurentian University, 1990.

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Bradley, Jean-Claude. A study of the reactivity of the carboxyl function in 1, 3, 4-oxadiazole-2-carboxylates. Laurentian University, 1989.

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Berlin, Freie Universität, ed. 3-Amino- und 3-Arylazo- 1,2,4-oxadiazol-5-one als neue NO-Donatoren. 1996.

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Kaur, Ms Rajwant. Synthesis and Antimicrobial Activity of 1,3,4-Oxadiazole Derivatives. Independently Published, 2018.

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Kayukova, L. A., A. V. Vologzhanina та E. M. Yergaliyeva. SPIROPYRAZOLINIUM COMPOUNDS AS A RESULT OF β-AMINOPROPIOAMIDOXIMES INTRAMOLECULAR REARRANGEMENTS. Daryn, Almaty, Kazakhstan, 2022. http://dx.doi.org/10.51580/2022-ebook.01.

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The monograph deals with unexpected rearrangements of β-aminopropioamidoxime derivatives, which form previously unknown spiropyrazolinium compounds. Recently we found that the 3,5-substituted 1,2,4-oxadiazoles, which are derivatives of β-aminopropioamidoximes, are of interest for practical medicine since they possess local anaesthetic, anti-tubercular and anti-diabetic properties. But when analyzing biological activity, it is necessary to take into account the chemical stability of the studied compounds. It turned out that 3,5-substituted 1,2,4-oxadiazoles taken for screening according to the
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Book chapters on the topic "Oxadiazol"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 6-(5-methyl-1,2,4-oxadiazol-3-yl)-2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_58.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 6-(5-methyl-1,2,4-oxadiazol-3-yl)-2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_59.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 6-(5-methyl-1,2,4-oxadiazol-3-yl)-2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_60.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 6-(5-methyl-1,2,4-oxadiazol-3-yl)-2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_61.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 6-(5-methyl-1,2,4-oxadiazol-3-yl)-2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_62.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with 6-(5-methyl-1,2,4-oxadiazol-3-yl)-2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_63.

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Rauf, Abdul, and Nida Nayyar Farshori. "Oxadiazoles." In SpringerBriefs in Molecular Science. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_5.

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Romeo, Giovanni, and Ugo Chiacchio. "Oxadiazoles." In Modern Heterocyclic Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527637737.ch13.

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Sahoo, Priya Ranjan, Abhishek Saxena, and Satish Kumar. "Oxadiazole as Inhibitors." In Oxadiazole in Material and Medicinal Chemistry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003384441-7.

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Chen, Chin-Hsiang, Ming-Han Yang, and Wei-Chi Lin. "GaN MIS Photodetectors with l,3-bis [2-(2,20-bipyridin-6–yl) -1,3,4-oxadiazol-5-yl]-benzene (Bpy-OXD) Insulators." In Lecture Notes in Electrical Engineering. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04573-3_138.

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Conference papers on the topic "Oxadiazol"

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Tyrkov, Alexey, Svetlana Luzhnova, Evgenia Utyaganova, and Ekaterina Yurtayeva. "Promising materials based on Tetrahydro-[1,2,4]Oxadiazole[3,2-C][1,4]Oxazine for innovative biotechnologies." In "The Caspian in the Digital Age" within the framework of the International Scientific Forum "Caspian 2021: Ways of Sustainable Development". Dela Press Publishing House, 2022. http://dx.doi.org/10.56199/dpcsebm.sddh5085.

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The synthesis of 2-[(1,3-diphenyl-1H-1,2,4-triazol-5-yl) dinitromethyl]-5,6,8,8a-tetrahydro-[1,2,4] oxadiazol[3,2-c][1,4] oxazine is caused by the reaction of morpholine interaction in the presence of hydrogen peroxide with 2-(1,3-diphenyl-1H-1,2,4-triazol-5-yl)-2,2-dinitroacetonitrile and sodium tungstate in a catalytic amount. The latter interacts with an excess of KOH in ethanol to form the potassium salt aci-5-dinitromethyl-1,3-diphenyl-1H-1,2,4-triazole and 5,6,8,8a-tetrahydro-[1,2,4] oxadiazole[3,2-c] [1,4] oxazine-2-ol. The ability of compounds 3-5 to inhibit the growth and development
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Malavolta, Juliana L., Alex F. C. Flores, Rayane B. Goularte, Alynne A. Souto, and Morgana Doneda. "Synthesis of new biheterocyclic 4-(2-(1,3,4-oxadiazol-2- yl)ethyl)-6-(trifluoromethyl)pyrimidines." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0107-1.

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Szafrański, Krzysztof, Jarosław Sławiński, and Anna Kawiak. "Optimization of 4-chloro-5-[5-(2-arylvinyl)-1,3,4-oxadiazol-2-yl]benzenesulfonamide structure towards anticancer activity." In 5th International Electronic Conference on Medicinal Chemistry. MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06318.

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Yarovenko, V., I. Zavarzin, and M. Krayushkin. "Convenient synthesis of 1,2,5-(1,3,4)-oxadiazolyl-1,2,4-oxadiazoles." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02051.

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Ahsan, Mohamed Jawed, and Sunil Shastri. "Synthesis of N-{[5-aryl/alkyl-1,3,4-oxadiazol-2-yl]methyl}pyridin-2-amine as Antimicrobial and Anticancer Agents." In 1st International Electronic Conference on Medicinal Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a029.

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Likhar, Rupali, and Tabassum Khan. "Design, Synthesis, Molecular Docking Studies, and Biological Evaluation of 1, 3, 4-oxadiazol-3(2H)-yl] Ethan-1-one Derivatives as Antimicrobial Agents." In International Electronic Conference on Medicinal Chemistry. MDPI, 2022. http://dx.doi.org/10.3390/ecmc2022-13247.

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Troitskaya-Markova, Nadezhda, Olga Vlasova та Oleg Rakitin. "4,5-DIOXO-4,5-DIHYDRO-4Λ4,5Λ4-BIS([1,2,5]OXADIAZOLO)[3,4-с:3',4'-e]PYRIDAZINE AS A SYNTHETIC EQUIVALENT OF 4,4'-DINITROSO-3,3'-BI(1,2,5-OXADIAZOLE)". У Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m779.aks-2019/305-307.

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Choy, Wallace C. H., K. N. Hui, Y. J. Liang, et al. "Oxadiazole-Triphenylamine derivatives for OLEDs." In Optics & Photonics 2005, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2005. http://dx.doi.org/10.1117/12.616721.

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M. AHMED, Riyadh, Sarah S. ABDUL RAHMAN, Dhefaf H. BADRI, Khawla M. SULTAN, Ismaeel Y. MAJEED, and Ghada M. KAMIL. "SYNTHESIS AND CHARACTERISATION OF NEW Co(II), Zn(II) AND Cd(II) COMPLEXES DERIVED FROM OXADIAZOLE LIGAND AND 1,10-PHENANTHROLINE AS Co-LIGAND." In V. International Scientific Congress of Pure, Applied and Technological Sciences. Rimar Academy, 2022. http://dx.doi.org/10.47832/minarcongress5-5.

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In this work, prepared new ligand namely 5-(2,4—dichloro-phenyl)-1,3,4- oxadiazole-2-(3H)-thion, which was obtained from the 2,4-dichlorobenzoyl chloride with hydrazine, after that reaction with CS2/KOH in methanol. This ligand was reaction with (Co, Zn and Cd) and 1,10-phenanthroline as co-ligand. The ligand and complexes were characterised by IR, UV-Vis, C-H-N, magnetic moment, A.A, Cl content, and m.p.. The data that collected indicate the octahedral geometry around metal ions in all complexes. In IR spectra of complexes, the small shift in ν(C=S), indicating the exocyclic sulfur is not bon
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Jung, Gun-Young, Changsheng Wang, Christopher Pearson, Martin R. Bryce, Ifor D. W. Samuel, and Michael C. Petty. "Electroluminescent devices incorporating a new oxadiazole derivative." In International Symposium on Optical Science and Technology, edited by Zakya H. Kafafi. SPIE, 2001. http://dx.doi.org/10.1117/12.416909.

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Reports on the topic "Oxadiazol"

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Byrd, Edward F., and Jesse J. Sabatini. Theoretical Prediction of the Heats of Formation, Densities and Relative Sensitivities, and/or Synthetic Approaches Toward the Synthesis of High Energy Dense Materials (HEDMs): 3,5-Dinitro-1,3,5-Oxadiazinane, Bis-Adjacent RDX, Bis-Adjacent HMX, 4,4',6,6'-Tetranitro-1,1'-Bis(N-oxide)-5,5',6,6'-4H,4'H-5,5'-Bisimidazo Oxadiazole, and the Open-Cage Derivative of CL-20. Defense Technical Information Center, 2015. http://dx.doi.org/10.21236/ada626921.

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