Academic literature on the topic '4-oxadiazole'

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Journal articles on the topic "4-oxadiazole"

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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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Bandeira, Gustavo Neto, Claudio Augusto Gomes da Camara, Marcílio Martins de Moraes, João Paulo Ramos de Melo, João Rufino de Freitas Filho, and Jucleiton José Rufino de Freitas. "Synthesis and Insecticidal Activity of 1,2,4-Oxadiazoles Derivates against (Plutella xylostella L.) Diamondback Moth." Archives of Current Research International 25, no. 1 (2025): 283–92. https://doi.org/10.9734/acri/2025/v25i11058.

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The diamondback moth (Plutella xylostella) is a cosmopolitan pest known for its destruction of cruciferous plants. Commercial insecticides, such as Decis 25 EC and Azamax, are the main forms of controlling this pest in irrigated systems in the agricultural communities of the city of Garanhuns (northeastern Brazil). However, the difficulty in controlling this pest resides in its high fecundity and short lifecycle, which serve as resistance mechanisms to insecticides. Considering the immediate need to find alternative products to insecticides employed in these agricultural communities, nine 1,2,
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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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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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Nisheeth, Rastogi, and Anil Harrison Darwin. "Synthesis and antifungal activity of some new derivatives of 5-{ 4' -(2" ,4"- dichlorobenzyloxy)-phenyl }-1 ,3,4-oxadiazole-2(3H)-thione." Journal of Indian Chemical Society Vol. 89, Nov 2012 (2012): 1543–50. https://doi.org/10.5281/zenodo.5771647.

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Department of Chemistry, Lucknow Christian Post-Graduate College, Lucknow-226 018, Uttar Pradesh, India <em>E-mail </em>: nisheethrastogi2003@gmail.com <em>Manuscript received 06 June 2011, revised OJ February 2012, accepted 08 February 2012</em> 5-{ 4&#39;-(2&quot; ,4&quot; -Dichlorobenzyloxy)-phenyl}-1,3,4-oxadiazole-2(3<em>H</em>)-thione (2) was prepared by the reaction of 4- (2&#39; ,4&#39; -dichlorobenzyloxy)-benzoylhydrazine (1) with potassium isopropylxanthate in isopropyl alcohol. 5-{ 4&#39; -(2&quot; ,4&quot;- Dichlorobenzyloxy)-phenyl}-1,3,4-oxadiazole-2(3<em>H</em>)-thione (2) on be
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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., Sapthagiri, Sriram R., Ilavarasan L., and Ravi A. "SYNTHESIS AND CHARACTERIZATION OF 2-AMINO-1, 3, 4-OXODIAZOLE DERIVATIVES." International Journal of Applied and Advanced Scientific Research 1, no. 2 (2017): 61–65. https://doi.org/10.5281/zenodo.258975.

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A simple protocol for the synthesis of 2-amino-1, 3, 4-oxadiazole derivatives using iodoaceticacid as a cyclodesulfurization agent. This method is also applicable to the synthesis of various substituted 2-amino-1, 3, 4-oxadiazole derivatives such as 5-(2-bromophenyl)-N-phenyl-1, 3, 4-oxadiazol-2-amine. The synthesized methodology was simple and hazardless, it’s giving good yield.
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Jin, Guoxia, Yuqi Ji, Teng Wang, et al. "Syntheses and characterization of dinuclear and tetranuclear AgI supramolecular complexes generated from symmetric and asymmetric molecular clips containing oxadiazole rings." Acta Crystallographica Section C Structural Chemistry 75, no. 10 (2019): 1327–35. http://dx.doi.org/10.1107/s2053229619011744.

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A new asymmetric ligand, 5-{3-[5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl]phenyl}-2-(pyridin-3-yl)-1,3,4-oxadiazole (L5), which contains two oxadiazole rings, was synthesized and characterized. The assembly of symmetric 2,5-bis(pyridin-3-yl)-1,3,4-oxadiazole (L1) and asymmetric L5 with AgCO2CF3 in solution yielded two novel AgI complexes, namely catena-poly[[di-μ-trifluoroacetato-disilver(I)]-bis[μ-2,5-bis(pyridin-3-yl)-1,3,4-oxadiazole]], [Ag2(C2F3O2)2(C12H8N4O)2] n or [Ag2(μ2-O2CCF3)2(L1)2] n (1), and bis(μ3-5-{3-[5-(4-methylphenyl)-1,3,4-oxadiazol-2-yl]phenyl}-2-(pyridin-3-yl)-1,3,4-oxadiazole
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Farah, Deeba, Abbas Naeem, Tahir Butt Muhammad, Ahmad Khan Rauf, Muneeb Ahsan Muhammad, and Ain Khan Misbahul. "Synthesis, characterization and biological activities of 1,3,4-oxadiazole derivatives of nalidixic acid and their copper complexes." Chemistry International 4, no. 4 (2018): 206–15. https://doi.org/10.5281/zenodo.1475387.

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A series of novel 1, 3, 4-oxadiazole analogues was synthesized from cyclization of hydrazones of substituted 1-ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carbohydrazides were prepared from nalidixic acid. The structures of synthesized oxadiazole derivatives and their copper complexes were elucidated on the basis of FTIR, elemental analyses, 1H-NMR and atomic absorption spectral analysis. It was observed from spectral data that metal ligand ratio was 1:1 in all copper complexes and they were bidentate, coordination was found to be done through oxygen of 4-oxo group and nitrogen of oxa
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Dissertations / Theses on the topic "4-oxadiazole"

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Kivrak, Arif. "Development Of New Methods For The Synthesis Of Pyrazoles, 4-iodopyrazoles, Isoxazoles And 1,2,4-oxadiazoles." Phd thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12612945/index.pdf.

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Synthesis of five-membered heteroaromatic compounds such as pyrazoles, isoxazoles and 1,2,4-oxadiazoles are important for pharmaceutical industry and material science due to their applications. Although there are many methods to prepare such compounds, new variants continue to appear since they exhibit a wide range of biological and medicinal activities. In this thesis, new methods were developed for the synthesis of 4-iodopyrazoles, pyrazoles, isoxazoles, 1,2,4-oxadiazoles and/or 1,2,4-oxadiazepines. In the first part of the study, electrophilic cyclization of &alpha<br>,&beta<br>-alkynic hy
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Le, Falher Laetitia. "Préparation et dérivatisation de 4H-pyrido[e][1,3]oxazinones : une contribution à la diversité chimique." Thesis, Paris 6, 2014. http://www.theses.fr/2014PA066344.

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Ce manuscrit porte sur la synthèse et les applications d'une nouvelle série de composés hétéroaromatiques : les 4H-pyrido[e][1,3]oxazin-4-ones. La première partie de ce manuscrit présente la préparation de ces squelettes via une réaction d'O-arylation intramoléculaire. La seconde partie du manuscrit repose sur la réactivité de ces entités chimiques et de leur utilisation en tant qu'intermédiaires de synthèse. La fonctionnalisation des 4H-pyrido[e][1,3]oxazin-4-ones, via des réactions de couplage pallado-catalysées, a permis d'obtenir des systèmes polyfonctionnalisés plus complexes. Les pyrido-
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Singh, Neeraj. "Generation of 4,5-Dihydro-1,2,3-oxadiazole and Study of the Decomposition Products." Doctoral thesis, Universitätsbibliothek Chemnitz, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-191706.

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4,5-Dihydro-1,2,3-oxadiazoles are postulated to be key intermediates in the synthesis of ketones from alkenes on an industrial scale, alkylation of DNA in vivo, decomposition of N-nitrosoureas (potent carcinogens), and are also a subject of great interest for theoretical chemists. In this thesis, formation of the parent compound and decay into secondary products has been studied by NMR monitoring analysis. The elusive properties and the intermediacy of the parent compound, 4,5-dihydro-1,2,3-oxadiazole, in the decomposition of suitably substituted N-nitrosoureas using Tl(I) alkoxides as bases,
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Wolf, Lucas. "Síntese de heterociclos: 2-alquil/arilcalcogeno-n-(4-aril-1,3-tiazol-2-il)acetamidas e (s)-n-(1-(3-aril-1,2,4-oxadiazol-5-il)alquil)-2-(calcogenofenil) acetamidas derivados de organocalcogênios." Universidade Federal de Santa Maria, 2015. http://repositorio.ufsm.br/handle/1/4271.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>In the present work, a series of 2-alkyl/arylchalcogenide-N-(4-aryl-1,3-thiazol-2-yl)acetamide was prepared via addition of aryl or alkyl chalcogenides. This methodology allowed the preparation of new derivatives of 2-amino-1,3-thiazoles in good yields. The compound synthesized is intended to evaluate the biological potential from the antioxidant activity by scavenging capacity of the assay by ABTS and DPPH. Was also developed a methodology for obtaining the compounds (S)-N-(alkyl-1-(3-aryl-1,2,4-oxadiazol-5-yl)-2-(phenylchalcogeni
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Paulo, TÃrcio de Freitas. "5-(4-PIRIDIL)-1,3,4-(OXADIAZOL)-2-TIOL E Na3[Fe(CN)5Hpyt].3H2O: SÃntese, caracterizaÃÃo e estudos de formaÃÃo de monocamadas automontadas." Universidade Federal do CearÃ, 2007. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=1418.

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Conselho Nacional de Desenvolvimento CientÃfico e TecnolÃgico<br>As espÃcies 5-(4-piridil)-1,3,4-oxadiazol-2-tiol (Hpyt) e [Fe(CN)5Hpyt]3- (FeHpyt) adsorvem espontaneamente sobre ouro formando monocamadas automontadas (SAM - "Self-Assembled Monolayers") das quais, de acordo com os dados eletroquÃmicos, apresentam defeitos ou nanoporos por onde as molÃculas de prova [Fe(CN)6]4â e [Ru(NH3)6]3+ acessam a superfÃcie do eletrodo de ouro policristalino. A partir dessas molÃculas de prova e da dependÃncia entre a corrente faradÃica e o pH do eletrÃlito, o pKa da monocamada de Hpyt foi calculada como
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Paulo, Tércio de Freitas. "5-(4-PIRIDIL)-1,3,4-(OXADIAZOL)-2-TIOL E Na3[Fe(CN)5Hpyt].3H2O: Síntese, caracterização e estudos de formação de monocamadas automontadas." reponame:Repositório Institucional da UFC, 2007. http://www.repositorio.ufc.br/handle/riufc/13715.

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PAULO, T. F.; DIÓGENES, I. C. N. 5-(4-PIRIDIL)-1,3,4-(OXADIAZOL)-2-TIOL E Na3[Fe(CN)5Hpyt].3H2O: Síntese, caracterização e estudos de formação de monocamadas automontadas. 2007. 85 f. Dissertação (Mestrado em Química Inorgânica) - Centro de Ciências, Universidade Federal do Ceará, Fortaleza, 2007.<br>Submitted by José Jairo Viana de Sousa (jairo@ufc.br) on 2014-10-15T17:50:25Z No. of bitstreams: 1 2007_dis_tfpaulo.pdf: 2052309 bytes, checksum: bfeda1bf390b31ae8ba8c29ee74f6e40 (MD5)<br>Approved for entry into archive by José Jairo Viana de Sousa(jairo@ufc.br) on 2015-10-22T23:18:53Z (GMT) No
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Ko, Changheui. "Optimization of bulkheterojunction organic photovoltaics structure/property study with oxadiazole contained poly(p-phenylene)s [OXA-PPVs] and device system engineering /." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 208 p, 2009. http://proquest.umi.com/pqdweb?did=1663060511&sid=4&Fmt=2&clientId=8331&RQT=309&VName=PQD.

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Riederer, Cordula. "Zur Synthese von Tetrahydro-oxazolo[4,3-c]-1,2,4-oxadiazol-5-onen und Tetrahydro-oxazolo[4,3-c]-1,2,4-oxadiazin-6-onen aus 4-Hydroxyimino-oxazolidin-2-onen." [S.l. : s.n.], 1999. http://www.sub.uni-hamburg.de/disse/68/riederer.PDF.

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Almeida, Leonardo Viana de. "Síntese e determinação da atividade antimicrobiana de 2-[5-nitro-tiofen-2-il]-3-acetil-5-[4-fenil-substituído]-2,3-diidro-1,3,4-oxadiazol frente à cepa ATCC 25923 de Staphylococcus aureus." Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/9/9135/tde-07042010-131506/.

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A introdução de um grupo substituinte na molécula de um fármaco promove alterações químico-estruturais que, por sua vez, modificam suas propriedades físicoquímicas. O arranjo espacial de átomos ou grupos de átomos, em especial grupos funcionais, na molécula de um fármaco, expressos por meio de suas propriedades físico-químicas, influenciam direta ou indiretamente na interação fármaco-receptor. Esta, por sua vez, determina aspectos farmacológicos e farmacocinéticos que influem na eficácia terapêutica do medicamento. Assim, uma série de compostos 2-[5-nitro-tiofen-2-il]-3-acetil-5-[4-fenil-subst
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Oliveira, Alex Alfredo de. "Planejamento, síntese, determinação da atividade biológica e estudos de QSAR-2D de derivados 1,3,4-oxadiazolínicos frente ao Trypanosoma cruzi." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/9/9135/tde-22122011-084355/.

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Doenças como malária, esquistossomose, filaríase linfática, dengue, leishmaniose e mal de Chagas são endêmicas em países tropicais. Referente ao período entre 1975 e 2004, apenas 1% dos 1.556 novos fármacos registrados foi destinado ao tratamento destas doenças. Somente a doença de Chagas possui aproximadamente 18 milhões de casos em todo mundo. Até o momento, a quimioterapia para o tratamento dessa antropozoonose constitui-se basicamente de dois fármacos, o nifurtimox, proscrito no Brasil, e o benznidazol. Estes fármacos, além de apresentarem vários efeitos colaterais, são pouco eficazes, o q
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Books on the topic "4-oxadiazole"

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

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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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Book chapters on the topic "4-oxadiazole"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) complex with 5-(4-methoxy-phenyl)-1,3,4-oxadiazole-2-thione containing ethylenediamine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_65.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(II) complex with 5-(4-pyridyl)-1,3,4-oxadiazole-2-thione containing 2,2′-bipyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_67.

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Sahoo, Priya Ranjan, Abhishek Saxena, and Satish Kumar. "Oxadiazole as Electrochromic Materials." In Oxadiazole in Material and Medicinal Chemistry. CRC Press, 2024. http://dx.doi.org/10.1201/9781003384441-4.

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Ambhore, Ajay N. "An Efficient Green Synthesis of Diphenyl Pyrazol-4-Yl-Thiopyridin-4-Yl-1,3,4-Oxadiazole Derivatives and Evaluation of Their Antimicrobial and Antioxidant Activity." In Modern Green Chemistry and Heterocyclic Compounds. Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780367276942-3.

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Khalid, Hira, Aziz-ur-Rehman, M. Athar Abbasi, et al. "Synthesis, Spectral Analysis and Biological Evaluation of 5-Substituted 1,3,4-Oxadiazole-2-yl-4-(Piperidin-1-ylsulfonyl)Benzyl Sulfide." In Emerging Trends in Chemical Sciences. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-60408-4_14.

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Rajendran, Pavitra, and Erumaipatty Rajagounder Nagarajan. "Fluorescent Polyimide in Sensing Applications." In Polyimides. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.99935.

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Potential advances in sensing can be made by conjugated polymers includes poly(p-phenylene), poly(p-phenylene vinylene), polyfluorene, and poly(thiophene). Among the most important classes of polymers are heterocyclic polymers, such as polyimides, because polyimide nanocomposites possess exceptional mechanical strength as well as chemical, mechanical and temperature resistance. Polyimide offers the potential of providing efficient sensors through its ability to work actively. There is evidence that fluorescent polyimide is efficient at detecting hazardous pollutants. Chemical modifications of
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Revanasiddappa, B. C., and E. V. S. Subrahmanyam. "Study on 1, 3, 4-Oxadiazole Derivatives as an Antibacterial and Antifungal Agents." In New Innovations in Chemistry and Biochemistry Vol. 2. Book Publisher International (a part of SCIENCEDOMAIN International), 2021. http://dx.doi.org/10.9734/bpi/nicb/v2/13095d.

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Conference papers on the topic "4-oxadiazole"

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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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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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Zhang, Wei, Junsheng Yu, Nana Wang, Chunhua Huang, and Yadong Jiang. "Efficient organic photovoltaic cells using 2-(4-biphenylyl)-5-phenyl-1,3,4-oxadiazole as an exciton blocking layer." In 5th International Symposium on Advanced Optical Manufacturing and Testing Technologies, edited by Ya-Dong Jiang, Bernard Kippelen, and Junsheng Yu. SPIE, 2010. http://dx.doi.org/10.1117/12.866815.

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Varvara, Simona, Gianina Damian, Camelia Berghian-Grosan, Maria Popa, and Florin Popa. "Corrosion inhibition of carbon steel in hydrochloric acid solution using 5-(4-Pyridyl)-1,3,4-oxadiazole-2-thiol." In 1st Corrosion and Materials Degradation Web Conference. MDPI, 2021. http://dx.doi.org/10.3390/cmdwc2021-10005.

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Abood, Zeid Hassan, Hayder Raheem Ali, and Hussein Ali Qabel. "Microwave synthesis of 2,3,5-trisubstituted-1,3-imidazolidin-4-ones bearing 1,3,4-oxadiazole moiety and preliminary evaluation of their antibacterial activity." In THE 7TH INTERNATIONAL CONFERENCE ON APPLIED SCIENCE AND TECHNOLOGY (ICAST 2019). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5123064.

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Sushma and S. Ananda. "Synthesis of hybrid nano CoO/2-(4-chlorophenyl)-5-(3,4-dimethoxyphenyl)-1,3,4-Oxadiazole: Characterization and its application for viscosity studies for lubrication and photo-degradation." In DAE SOLID STATE PHYSICS SYMPOSIUM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0017530.

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saki, zeinab, Ali Kakanejadifard, Abedin Zabardasti, Farideh Azarbani, and Sahar Kakanejadifard. "Synthesis, characterization, solvatochromic, antioxidant and antibacterial activities investigation of 2,2'-((1E,1'E)-((1,2,5-oxadiazole-3,4-diyl)bis (azanylylidene))bis(methanylylidene))bis(4-(phenyldiazenyl)phenol)." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a047.

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Saleh, R. A., H. A. Mohammad, T. I. Gerber, and E. C. Hosten. "Synthesis and characterization of mono and mixed ligand, Ni(II), Pd(II) and Pt(II) complexes of S-5-phenyl-1, 3, 4-oxadiazole-2-yl benzothioate with some tertiary diphosphines ligands." In 6TH INTERNATIONAL CONFERENCE AND WORKSHOPS ON BASIC AND APPLIED SCIENCES. Author(s), 2017. http://dx.doi.org/10.1063/1.5004324.

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Forostyanko, Anna, Elena Vasileva, and Irina Proskurina. "SYNTHESIS OF 5-(4’-NITROPHENYL)-3-ARYL-1,2,4-OXADIAZOLES." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m758.aks-2019/222-226.

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Stadlbauer, Wolfgang, Corinna Gressl, A. Elisabeth Täubl, and Werner Fiala. "Cyclization of 4-Azido-3-nitroquinolines to Oxadiazolo[3,4-c]quinolines." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00487.

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Reports on the topic "4-oxadiazole"

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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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