Academic literature on the topic 'Oxadiazole derivative'

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Journal articles on the topic "Oxadiazole derivative"

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Rachel, Mathew* V. .S. Anjana Ayoona Najeeb Fathima Shereen S. Nikhila Anna Anil Saranya B. Sarin Santhosh. "COMMENCEMENT SCRUTINY OF 1,3,4-OXADIAZOLE; ITS VISCERAL ACTIVITIES." International Journal in Pharmaceutical Sciences 2, no. 5 (2024): 1265–74. https://doi.org/10.5281/zenodo.11264100.

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Oxadiazoles are a class of heterocyclic aromatic chemical compound of the azole family.1,3,4-oxadiazole is a nitrogen and oxygen containing heterocyclic derivative in which nitrogen in 3rd and 4th positions and oxygen in 1st position with chemical formula, C2 H2N2O and molecular weight 70.051g.mol-1. 1,3,4- oxadiazole is also known asOxdiazole,1-Oxa-3,4diazacyclopentadiene. 1,3,4- oxadiazole and its derivatives were used by several chemists for therapeutic conditions because it posses many pharmacological activities. 1,3,4- oxadiazole and its derivatives have great significance in medicinal ch
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Amer, Hamada, Omar Ali, Akram Salama, Marwa gendy та Omima Houssin. "Synthesis of some new 1,3,4-oxadiazole derivatives bearing sugars and α-aminophosphonate derived from 4-nitrophenol as anticancer agents". National Journal of Physiology, Pharmacy and Pharmacology 2, № 1 (2018): 1275. https://doi.org/10.5455/njppp.2018.8.0416408052018-1.

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Background: 1,3,4-oxadiazoles square measure a very important category of heterocyclic compounds with a broad variety of biological activities such as medicament, analgesic, ulcerogenicity, apoptosis inducer, anti-mycobacterial, antifungal, antitumor, P-glycoprotein Inhibitors, pesticides, 4-hydroxylase inhibitors, and antiepileptic drug activity. Aims and Objectives: The present study is undertaken to study the evaluation of new 1,3,4-oxadiazole derivatives bearing sugars and α-aminophosphonate derived from 4-nitrophenol as anticancer agents. Materials and Methods: A sequence of acyclic nucle
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Santhanalakshmi K., Neelakandeswari N., Jacquline Rosy P., and Margandan K. "An In Vitro Evaluation of Anti-Inflammatory Activity of Newly Synthesized 1,3,4 Oxadiazole Derivatives." International Journal of Zoological Investigations 08, no. 02 (2022): 755–64. http://dx.doi.org/10.33745/ijzi.2022.v08i02.091.

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In the area of heterocyclic chemistry, oxadiazole has made major contributions. An enormous number of oxadiazoles have been synthesized and exposed to biological screening; the screening results improved their status due to its potential activities and their efficacy in diverse fields of daily life. Due to its wide range of pharmacological and therapeutic effects, the 1,3,4-oxadiazole moiety is the most important oxadiazole. In this study, we discuss a new family of 2,5-disubstituted 1,3,4-oxadiazole compounds' anti-inflammatory characteristics (4a-4h).The antiinflammatory efficacy of the oxad
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Ho, Vien Q. T., Mark K. Rong, Eva Habjan, et al. "Dysregulation of Mycobacterium marinum ESX-5 Secretion by Novel 1,2,4-oxadiazoles." Biomolecules 13, no. 2 (2023): 211. http://dx.doi.org/10.3390/biom13020211.

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The ESX-5 secretion system is essential for the viability and virulence of slow-growing pathogenic mycobacterial species. In this study, we identified a 1,2,4-oxadiazole derivative as a putative effector of the ESX-5 secretion system. We confirmed that this 1,2,4-oxadiazole and several newly synthesized derivatives inhibited the ESX-5-dependent secretion of active lipase LipY by Mycobacterium marinum (M. marinum). Despite reduced lipase activity, we did not observe a defect in LipY secretion itself. Moreover, we found that several other ESX-5 substrates, especially the high molecular-weight PE
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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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Qazi, Adil Iqbal, Bashir Ahmad, Muhammad Umar Khayam Sahibzada, et al. "Evaluation of Antidiabetic Activity of Oxadiazole Derivative in Rats." Evidence-Based Complementary and Alternative Medicine 2023 (April 25, 2023): 1–15. http://dx.doi.org/10.1155/2023/1141554.

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The oxadiazole ring has long been used for the treatment of several diseases. This study aimed to analyze the antihyperglycemic and antioxidant roles of the 1,3,4-oxadiazole derivative with its toxicity. Diabetes was induced through intraperitoneal administration of alloxan monohydrate at 150 mg/kg in rats. Glimepiride and acarbose were used as standards. Rats were divided into groups of normal control, disease control, standard, and diabetic rats (treated with 5, 10, and 15 mg/kg of 1,3,4-oxadiazole derivative). After 14 days of oral administration of 1,3,4-oxadiazole derivatives (5, 10, and
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Irfan, Ali, Shah Faisal, Ameer Fawad Zahoor, et al. "In Silico Development of Novel Benzofuran-1,3,4-Oxadiazoles as Lead Inhibitors of M. tuberculosis Polyketide Synthase 13." Pharmaceuticals 16, no. 6 (2023): 829. http://dx.doi.org/10.3390/ph16060829.

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Benzofuran and 1,3,4-oxadiazole are privileged and versatile heterocyclic pharmacophores which display a broad spectrum of biological and pharmacological therapeutic potential against a wide variety of diseases. This article reports in silico CADD (computer-aided drug design) and molecular hybridization approaches for the evaluation of the chemotherapeutic efficacy of 16 S-linked N-phenyl acetamide moiety containing benzofuran-1,3,4-oxadiazole scaffolds BF1–BF16. This virtual screening was carried out to discover and assess the chemotherapeutic efficacy of BF1–BF16 structural motifs as Mycobac
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Ramazani, Ali, Yavar Ahmadi, and Fatemeh Zeinali Nasrabadi. "Four-component Synthesis of 1,3,4-Oxadiazole Derivatives from (N-Isocyanimino)triphenylphosphorane, (E)-Cinnamic Acids, Acetaldehyde and Secondary Amines." Zeitschrift für Naturforschung B 66, no. 2 (2011): 184–90. http://dx.doi.org/10.1515/znb-2011-0211.

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The 1 : 1 iminium intermediate, generated by the addition of a secondary amine to acetaldehyde is trapped by the (N-isocyanimino)triphenylphosphorane in the presence of an (E)-cinnamic acid derivative, leading to the formation of the corresponding iminophosphorane intermediate. Disubstituted 1,3,4-oxadiazole derivatives are formed via intramolecular aza-Wittig reaction of the iminophosphorane intermediates. The reactions were completed under neutral conditions at room temperature, and the corresponding disubstituted 1,3,4-oxadiazole derivatives were produced in excellent yields.
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Das, Rina, and Dinesh Kumar Mehta. "Evaluation and Docking Study of Pyrazine Containing 1, 3, 4-Oxadiazoles Clubbed with Substituted Azetidin-2-one: A New Class of Potential Antimicrobial and Antitubercular." Drug Research 71, no. 01 (2020): 26–35. http://dx.doi.org/10.1055/a-1252-2378.

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Abstract Background Tuberculosis (TB) caused by Mycobacterium tuberculosis is one of the main killers of people all over the world. The major hurdles with existing therapy are the lengthy regimen and appearance of multi drug resistant (MDR) and extensively drug resistant (XDR) strains of M.tuberculosis. Aims The present work was aimed to synthesize and determine antitubercular and antimicrobial potential of some novel 3-chloro-4-aryl-1-[4-(5-pyrazin-2-yl[1,3,4]oxadiazole-2-ylmethoxy)-phenyl]-azetidin-2-one derivatives 7(a-h) from pyrazinoic acid as precursor, which is a well-established antitu
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Ekram Abdullah Basheer, Kalid Matny Al-jaanaby, and Feras Shauki Al-joboury. "Synthesis a Number of Heterocyclic Compounds Derived From Levofloxacin." Tikrit Journal of Pure Science 20, no. 5 (2023): 84–95. http://dx.doi.org/10.25130/tjps.v20i5.1244.

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In this paper, the preparation a number of heterocyclic compounds five membered rings like oxadiazole, imidazolidine, thiozolidine, tetrazole, azetidine 2-on. Hydrazide (1) was synthesized from the reaction of levofloxacin with hydrazine hydrate. Hydrazone compounds (2-9) were synthesized from the reaction (1) with a number of aldehydes, and 3-acetyl-1,3,4-oxadiazol (10-17) was prepared from the reaction of hydrazones (2-9) with acetic anhydride, 5-oxo-2-aryl imadazoldine derivative (18-25) were prepared from the reaction of hydrazone derivatives (2-9) with glycine, while the reaction of hydra
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Dissertations / Theses on the topic "Oxadiazole derivative"

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Mayr, Norbert. "Energetic materials based on isocyanuric acid and 1,2,4-oxadiazole derivatives." Diss., Ludwig-Maximilians-Universität München, 2013. http://nbn-resolving.de/urn:nbn:de:bvb:19-162379.

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The synthesis and properties of explosive urea and triazine derivatives is investigated on behalf of the explosive parameters and the full characterization of the molecules. (Chapter I-III) The class of oxadiazole derivatives is enhanced from the known explosive 1,2,5 oxadiazole (furazane) derivatives to the 1,2,4 oxadiazole derivatives. This molecule class is thoroughly investigated by all terms of chemical and explosive material matter and especially the 1,2,4-oxadiazol-5-one derivatives are compared to the corresponding tetrazole derivatives which were by far the most investigated molecule
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Xü, Chenggang. "Preparation and characterization of vapour deposited films based on substituted 2,5-diphenyl-1,3,4-oxadiazole derivatives." Phd thesis, Universität Potsdam, 2004. http://opus.kobv.de/ubp/volltexte/2005/102/.

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Diese Arbeit befasst sich mit dem Einfluss der molekularen Struktur von 2,5-Diphenyl-1,3,4-Oxadiazol-Derivaten auf die Präparierung dünner Schichten mittels Vakuumdeposition. Dünne Schichten von diesen Substanzen wurden auf Si/SiO2 aufgedampft und ihre Struktur systematisch mittels XSR, AFM und IR untersucht. Das Ergebnis zeigt, dass die Schichtstrukturen offenbar von Substratetemperatur (Ts) abhängig sind. Im untersuchten Ts-Bereich bilden etherverbrückte Oxadiazole immer geordnete Schichten und die Schichtperiodicität hängt linear von der Längen der aliphatischen Ketten, während sich bei den
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Franco, González Olga. "Structural and spectroscopical study of crystals of 1,3,4-oxadiazole derivatives at high pressure." [S.l. : s.n.], 2002. http://pub.ub.uni-potsdam.de/2002/0026/franco.pdf.

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Franco, González Olga. "Structural and spectroscopical study of crystals of 1,3,4-oxadiazole derivatives at high pressure." Phd thesis, Universität Potsdam, 2002. http://opus.kobv.de/ubp/volltexte/2005/53/.

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Die Suche nach neuen Materialien von technischem Interesse hat in den letzten Jahren neue Antriebe zu der Untersuchung organischer Verbindungen gegeben. Organische Substanzen haben viele Vorteile wie z.B. die Möglichkeit, ihre Eigenschaften durch verschiedene chemische und physikalische Techniken im Herstellung-Prozess für ein bestimmtes Ziel zu modifizieren. Oxadiazolverbindungen sind interessant aufgrund ihrer Nutzung als Material für Licht emittierende Dioden und Scintillatoren. <br /> <br /> Die physikalischen Eigenschaften eines Festkörpers hängen von seiner Struktur ab. Unterschiedliche
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Krake, Susann H. "Antiviral Agents: 3,5-Disubstituted 1,2,4-Oxadiazole Derivatives and Novel Peptidomimetics Containing Hydroxyethyl Isostere and Imidazolidinone Structures." Ohio University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1357572368.

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Xü, Chenggang. "Preparation and characterization of vapour deposited films based on substituted 2,5-diphenyl-1,3,4-oxadiazole derivatives." [S.l.] : [s.n.], 2004. http://pub.ub.uni-potsdam.de/2004/0035/xucg.pdf.

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Masciocchi, D. "DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF POTENTIAL STAT3 INHIBITORS AS ANTICANCER AGENTS." Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/170266.

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Signal Transducers and Activators of Transcription factors (STATs) are a class of latent cytoplasmic proteins that regulate cell growth and survival by modulating the expression of specific target genes. One member of the STAT family, STAT3, has received particular attention since it has been found constitutively activated in a broad spectrum of cancer cell lines and human tumors. These compelling results, combined with a well-known selectivity of STAT3 inhibitors for tumor cells, validated STAT3 as a promising anticancer drug target. Although the experimental studies on STAT3 inhibitors seem
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Rowe, David Martin. "Investigations of the synthesis of new photochromic oxazine and oxadiazine derivatives." Thesis, University of Edinburgh, 1996. http://hdl.handle.net/1842/12884.

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This thesis is concerned with the investigation of new synthetic routes to novel oxazine and oxadiazine derivatives which are of potential photochromic importance. A general synthetic strategy for the synthesis of 2,2-disubstituted 2H-benz-1,4-oxazines based on the synthesis of 2-nitrophenoxyacetaldehydes and their reductive cyclisation via a situ ring closure of intermediate 2-aminophenoxyacetaldehydes was investigated. Various attempts having failed to achieve the reductive cyclisation of the 2-nitrophenoxyacetaldehydes to the 2H-benz-1,4-oxazines, attention was turned to an alternative appr
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Conde, Amanda Solis. "Synthesis of 5-methyl-3-phenyl-1,3,4-oxadiazol-2(3H)-one derivatives by electrophilic aromatic substitution." Wright State University / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=wright1547584724393162.

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Mayr, Norbert Verfasser], and Thomas M. [Akademischer Betreuer] [Klapötke. "Energetic materials based on isocyanuric acid and 1,2,4-oxadiazole derivatives : synthesis and characterization / Norbert Mayr. Betreuer: Thomas M. Klapötke." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2013. http://d-nb.info/1044532246/34.

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Books on the topic "Oxadiazole derivative"

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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 "Oxadiazole derivative"

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Qian, Xuhong, Song Cao, Zhong Li, Gonghua Song, and Qingchun Huang. "Oxadiazole Derivatives as Novel Insect-Growth Regulators: Synthesis and Structure—Bioactivity Relationship." In ACS Symposium Series. American Chemical Society, 2004. http://dx.doi.org/10.1021/bk-2005-0892.ch026.

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Desai, Kishor R., and Bhavin R. Patel. "Various Synthetic Strategies and Therapeutic Potential of Thiadiazole, Oxadiazole, Isoxazole and Isothiazole Derivatives." In N-Heterocycles. Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0832-3_6.

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Gujjarappa, Raghuram, Sattu Sravani, Arup K. Kabi, et al. "An Overview on Biological Activities of Oxazole, Isoxazoles and 1,2,4-Oxadiazoles Derivatives." In Materials Horizons: From Nature to Nanomaterials. Springer Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-8399-2_10.

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Dekate, Shital M., Kishor M. Hatzade, and Ajay M. Ghatole. "Design, Synthesis, and Characterization of Some Oxadiazole Derivatives and Their S-Glucosides Bearing Thiazole Scaffold." In Springer Proceedings in Materials. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-97-5169-3_20.

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Mohamad, Hikmat Ali, and Beriwan Mohamad Hamad Ameem. "Synthesis and Characterization of Co(II), Ni(II) and Cu(II) Complexes with Thio-1,3,4-oxadiazole Derivatives." In Crystallizing Ideas – The Role of Chemistry. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31759-5_17.

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Posokhov, Yevgen O., Alexander Kyrychenko, and Yevgen Korniyenko. "Derivatives of 2,5-Diaryl-1,3-Oxazole and 2,5-Diaryl-1,3,4-Oxadiazole as Environment-Sensitive Fluorescent Probes for Studies of Biological Membranes." In Reviews in Fluorescence 2017. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-01569-5_9.

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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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Casu, M. B., P. Imperia, S. Schrader, B. Schulz, F. Fangmeyer, and H. Schürmann. "Electronic Structure of Ordered Langmuir-Blodgett Films of an Amphiphilic Derivative of 2,5-Diphenyl-1,3,4-Oxadiazole." In Studies in Interface Science. Elsevier, 2001. http://dx.doi.org/10.1016/s1383-7303(01)80021-1.

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Keertika, Bentham Science Publisher, and Nutan Sharma. "Oxazole, Oxadiazole, Isoxazoline and Oxazoline Derivatives as Anti-Inflammatory Agents." In Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815223460124010007.

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Oxygen and Nitrogen containing five-membered heterocyclic compounds have been the target of intense investigation in the last two decades to discover potent biologically active compounds as anti-inflammatory agents. The related studies comprising of fascinating oxazole-based derivatives include oxazoles, isoxazoles, oxazolines, and oxadiazoles, as therapeutic agents, which have become an interesting topic.Therefore, noticeable achievements have been accomplished in the field of antiinflammatory studies. This chapter will discuss some latest updates on the synthesis and anti-inflammatory studie
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Kanemasa, S. "Thermolysis of 1,2,5-Oxadiazole 2-Oxides (Furoxans)." In Three Carbon-Heteroatom Bonds: Nitriles, Isocyanides, and Derivatives. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-019-00010.

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Conference papers on the topic "Oxadiazole derivative"

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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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Fan, Rong, Dragana Culjkovic, Pongpun Piromreun, et al. "Light-emitting diodes based on a liquid-crystalline oxadiazole derivative." In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, edited by Zakya H. Kafafi. SPIE, 1999. http://dx.doi.org/10.1117/12.372707.

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Huang, Wei, Chang Liu, Ying Qian, et al. "Green frequency upconversion fluorescence of symmetrical 1,3,4-oxadiazole derivative by femtosecond three-photon excitation." In Photonics Asia 2007, edited by Yiping Cui, Qihuang Gong, and Yuen-Ron Shen. SPIE, 2007. http://dx.doi.org/10.1117/12.757341.

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Jesse, Kate, Sergio Diaz Abad, Christopher Van Pelt, Emily Pentzer, Benjamin Davis, and Sandipkumar Maurya. "Exploring Oxadiazole Derivative as Anolytes for &gt;3 V Non-Aqueous Redox Flow Battery." In American Chemical Society (ACS) National Meeting & Exposition - Fall ; 2024-08-18 - 2024-08-22. US DOE, 2024. http://dx.doi.org/10.2172/2467361.

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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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Stecoza, Camelia Elena, George Mihai Nitulescu, Constantin Draghici, et al. "New 1,3,4-oxadiazole derivatives and their role in tumor processes." In 7th International Electronic Conference on Medicinal Chemistry. MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11475.

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Tiuleanu, Pavel, Ivan Marenin, and Andrei Shchekotikhin. "Synthesis and evaluation of new 2-azolylindoles - derivatives of indole-2-carboxylic." In Conferința științifică națională cu participare internațională "Integrare prin cercetare și inovare", dedicată Zilei Internaționale a Științei pentru Pace și Dezvoltare. Moldova State University, 2025. https://doi.org/10.59295/spd2024n.91.

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Indole-2-carboxylic acid is a promising scaffold for the design of new compounds with application in biological studies and medicine practice. Its derivatives have shown a wide range of biological activity: antiviral, antifungal, antibacterial, anti-inflammatory. As part of the presented study, the method for preparation of alkyl derivatives of acetoacetic ester has been optimized. These derivatives are intermediates for the synthesis of indole-2-carboxylic acid esters according to the Japp-Klingemann/Fisher methodology. Several methods for the transformation of indole-2-carboxylic acid ester
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Kokate, Siddhant V., and Sachin V. Patil. "Synthesis and Antimicrobial Screening of Some New Thiazole Substituted 1,3,4-Oxadiazole Derivatives." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11662.

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"A quantitative structure-antioxidant relationship model for 1,3,4-oxadiazole derivatives using PLS regression." In 5th International Conference on Applied Science Energy and Environment. Ishik University, 2018. http://dx.doi.org/10.23918/icasee2018.03.

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Teng, Hsu-Tun, Meng-Hsiu Wu, Jiun-Haw Lee, Chun-Chieh Chao, Hung-Lin Chen, and Man-Kit Leung. "Oxadiazole derivatives used as the host of the metal doped electron transport layer material." In Optics & Photonics 2005, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2005. http://dx.doi.org/10.1117/12.617098.

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Reports on the topic "Oxadiazole derivative"

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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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