Relevant bibliographies by topics / Oxazol

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

Academic literature on the topic 'Oxazol'

Author: Grafiati
Published: 4 June 2021
Last updated: 3 February 2022

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Journal articles on the topic "Oxazol"

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Ochędzan-Siodłak, Wioletta, Dawid Siodłak, Karolina Banaś, Katarzyna Halikowska, Sławomir Wierzba, and Karel Doležal. "Naturally Occurring Oxazole Structural Units as Ligands of Vanadium Catalysts for Ethylene-Norbornene (Co)polymerization." Catalysts 11, no. 8 (2021): 923. http://dx.doi.org/10.3390/catal11080923.

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1,3-Oxazole and 4,5-dihydro-1,3-oxazole are common structural motifs in naturally occurring peptides. A series of vanadium complexes were synthesized using VCl3(THF)3 and methyl substituted (4,5-dihydro-1,3-oxazol-2-yl)-1,3-oxazoles as ligands and analyzed using NMR and MS methods. The complexes were found to be active catalysts both in ethylene polymerization and ethylene-norbornene copolymerization. The position of methyl substituent in the ligand has considerable impact on the performance of (co)polymerization reaction, as well as on the microstructure, and thus physical properties of the o
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Apostol, Theodora-Venera, Mariana Carmen Chifiriuc, Constantin Draghici, et al. "Synthesis, In Silico and In Vitro Evaluation of Antimicrobial and Toxicity Features of New 4-[(4-Chlorophenyl)sulfonyl]benzoic Acid Derivatives." Molecules 26, no. 16 (2021): 5107. http://dx.doi.org/10.3390/molecules26165107.

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The multi-step synthesis, physico-chemical characterization, and biological activity of novel valine-derived compounds, i.e., N-acyl-α-amino acids, 1,3-oxazol-5(4H)-ones, N-acyl-α-amino ketones, and 1,3-oxazoles derivatives, bearing a 4-[(4-chlorophenyl)sulfonyl]phenyl moiety are reported here. The structures of the newly synthesized compounds were confirmed by spectral (UV-Vis, FT-IR, MS, 1H- and 13C-NMR) data and elemental analysis results, and their purity was determined by RP-HPLC. The new compounds were assessed for their antimicrobial activity and toxicity to aquatic crustacean Daphnia m
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Rosca, Elena Valentina, Theodora Venera Apostol, Constantin Draghici, et al. "Synthesis, characterization and Cytotoxicity Evaluation of New Compounds from Oxazol-5(4H)-Ones and 1,2,4-Triazin-6(5H)-Ones Classes." Revista de Chimie 70, no. 11 (2019): 3769–74. http://dx.doi.org/10.37358/rc.19.11.7644.

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This paper presents the synthesis of new heterocyclic compounds from oxazoles and triazinones classes. Some 2-(4-(4-X-phenylsulfonyl)benzamido)acetic acids were condensed with 4-iodobenzaldehyde in presence of acetic anhydride and sodium acetate, when the new corresponding unsaturated oxazol-5(4H)-one were obtained. Through the reaction of these oxazol-5(4H)-ones with phenylhydrazine, in presence of the acetic acid and sodium acetate, the new heterocyclic compounds from 1,2,4-triazin-6(5H)-ones class were obtained. The structures of synthesized compounds have been confirmed by spectral methods
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Rosca, Elena Valentina, Theodora Venera Apostol, Constantin Draghici, et al. "Synthesis, characterization and Cytotoxicity Evaluation of New Compounds from Oxazol-5(4H)-Ones and 1,2,4-Triazin-6(5H)-Ones Classes." Revista de Chimie 70, no. 11 (2019): 3769–74. http://dx.doi.org/10.37358/rc.70.19.11.7644.

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This paper presents the synthesis of new heterocyclic compounds from oxazoles and triazinones classes. Some 2-(4-(4-X-phenylsulfonyl)benzamido)acetic acids were condensed with 4-iodobenzaldehyde in presence of acetic anhydride and sodium acetate, when the new corresponding unsaturated oxazol-5(4H)-one were obtained. Through the reaction of these oxazol-5(4H)-ones with phenylhydrazine, in presence of the acetic acid and sodium acetate, the new heterocyclic compounds from 1,2,4-triazin-6(5H)-ones class were obtained. The structures of synthesized compounds have been confirmed by spectral methods
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Zreigh, Mohamed M., Harry Adams, Richard F. W. Jackson, and Craig C. Robertson. "The first crystal structure of the pyrrolo[1,2-c]oxazole ring system." Acta Crystallographica Section E Crystallographic Communications 75, no. 9 (2019): 1336–38. http://dx.doi.org/10.1107/s2056989019011095.

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The title compound, C7H4F3NO2, 3-trifluoromethyl-1H-pyrrolo[1,2-c]oxazol-1-one, is the first crystal structure of the pyrrolo[1,2-c]oxazole ring system: the fused ring system is almost planar (r.m.s. deviation = 0.006 Å). In the crystal, weak C—H...O and C—H...F hydrogen bonds link the molecules into [001] chains and π–π stacking interactions consolidate the structure.
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Aly, Ashraf A., Alaa A. Hassan, Nasr K. Mohamed, et al. "Synthesis of New Fused Heterocyclic 2-Quinolones and 3-Alkanonyl-4-Hydroxy-2-Quinolones." Molecules 24, no. 20 (2019): 3782. http://dx.doi.org/10.3390/molecules24203782.

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Herein, we report the synthesis of 5,12-dihydropyrazino[2,3-c:5,6-c′]difuro[2,3-c:4,5-c′]-diquinoline-6,14(5H,12H)diones, 2-(4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)-1,4-diphenyl- butane-1,4-diones and 4-(benzo-[d]oxazol-2-yl)-3-hydroxy-1H-[4,5]oxazolo[3,2-a]pyridine-1-one. The new candidates were synthesized and identified by different spectroscopic techniques, and X-ray crystallography.
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Phalke, Pallavi L. "Synthesis of different α, β- unsaturated oxazolone derivatives". Journal of Drug Delivery and Therapeutics 9, № 1 (2019): 124–27. http://dx.doi.org/10.22270/jddt.v9i1.2189.

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Acetyl glycine were prepared from glycine acetic anhydride and then 2, 4-disubstituted Oxazol-5-one were prepared from acetyl glycine, substituted aldehydes, acetic anhydride, and sodium acetate as a catalyst. The formed product is evaluated and characterized by thin layer chromatography, infrared spectroscopy and melting point. The, β- unsaturated shows ability to react with various nucleophilic reagents for synthesis of new fused oxazole compounds.
 Keywords: glycine, acetic anhydride, aldehyde Sodium acetate, Oxazolone, E. coli, Antibacterial Activity.
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Ochędzan-Siodłak, Wioletta, Dawid Siodłak, Aleksandra Piontek, and Karel Doležal. "Titanium and Vanadium Catalysts with 2-Hydroxyphenyloxazoline and Oxazine Ligands for Ethylene-Norbornene (co)Polymerization." Catalysts 9, no. 12 (2019): 1041. http://dx.doi.org/10.3390/catal9121041.

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A series of titanium and vanadium complexes with oxazoline 2-(4,5-dihydro-1,3-oxazol-2-yl)phenol (L1), 2-(4-methyl-4,5-dihydro-1,3-oxazol-2-yl)phenol (L2), and oxazine 2-(5,6-dihydro-4H-1,3-oxazin-2-yl)phenol (L3) ligands were synthesized, and their structures were determined by NMR and MS methods as (L)2MtCl2. The vanadium complexes were found to be highly active in ethylene (7300 kgPE/(molV·h)) and ethylene/norbornene (5300 kgCop/(molV·h)) (co)polymerization. The polyethylene characteristics were melting temperature (123–142 °C), crystallinity degree (49–75%), molecular weight (5.7–8.5 × 105
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da Silva Filho, Antonio João, Lucinêz da Cruz Dantas, and Otávio Luís de Santana. "Diradicalar Character and Ring Stability of Mesoionic Heterocyclic Oxazoles and Thiazoles by Ab Initio Mono and Multi-Reference Methods." Molecules 25, no. 19 (2020): 4524. http://dx.doi.org/10.3390/molecules25194524.

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Mesoionics are neutral compounds that cannot be represented by a fully covalent or purely ionic structure. Among the possible mesomeric structures of these compounds are the diradical electronic configurations. Theoretical and experimental studies indicate that some mesoionic rings are unstable, which may be related to a significant diradical character, that until then is not quantified. In this work, we investigated the diradical character of four heterocycles: 1,3-oxazol-5-one, 1,3-oxazol-5-thione, 1,3-thiazole-5-one, and 1,3-thiazole-5-thione. The oxazoles are known to be significatively le
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Gelmi, M. Luisa, Donate Pocar, Monica Viziano, Riccardo Destro, and Felicita Merati. "Oxazol-5(4H)-ones. Part 7. New synthesis of oxazolo[5,4-b]pyridines." Journal of the Chemical Society, Perkin Transactions 1, no. 6 (1992): 701. http://dx.doi.org/10.1039/p19920000701.

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Dissertations / Theses on the topic "Oxazol"

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Santos, Daniela Rubia dos, Ieda Maria Begnini, and Universidade Regional de Blumenau Programa de Pós-Graduação em Química. "Síntese de cristais líquidos derivados dos heterociclos oxazol e tetrazol /." reponame:Biblioteca Digital de Teses e Dissertações FURB, 2006. http://www.bc.furb.br/docs/TE/2006/317236_1_1.pdf.

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Dantas, Lucinêz da Cruz. "Estudo do caráter dirradicalar de compostos da classe 1,3-Oxazol e 1,3-Tiazol." Universidade Federal da Paraí­ba, 2013. http://tede.biblioteca.ufpb.br:8080/handle/tede/7095.

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Made available in DSpace on 2015-05-14T13:21:22Z (GMT). No. of bitstreams: 1 ArquivoTotalLucinez.pdf: 2070839 bytes, checksum: 3d56c7860a648e855f328fcab8ae6afb (MD5) Previous issue date: 2013-05-27<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>The mesoionic compounds can not be represented by a purely ionic or covalent structure. Are neutral compounds that have well-separated regions of positive and negative charges, leading to a high dipole moment. They show wide range of applications, through biology and medicinal chemistry, as well in the obtaining produc
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Mello, Amanda Catharino de. "Obtenção de derivados de 1,3-oxazol através de reações de inserção envolvendo azalactonas e diazocompostos." Universidade Federal de Juiz de Fora (UFJF), 2018. https://repositorio.ufjf.br/jspui/handle/ufjf/7886.

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Submitted by Geandra Rodrigues (geandrar@gmail.com) on 2018-10-11T13:35:50Z No. of bitstreams: 1 amandacatharinodemello.pdf: 10070208 bytes, checksum: b00c39e2e5a28a1be7b81ed6260d151b (MD5)<br>Approved for entry into archive by Adriana Oliveira (adriana.oliveira@ufjf.edu.br) on 2018-10-16T13:59:05Z (GMT) No. of bitstreams: 1 amandacatharinodemello.pdf: 10070208 bytes, checksum: b00c39e2e5a28a1be7b81ed6260d151b (MD5)<br>Made available in DSpace on 2018-10-16T13:59:06Z (GMT). No. of bitstreams: 1 amandacatharinodemello.pdf: 10070208 bytes, checksum: b00c39e2e5a28a1be7b81ed6260d151b (MD5) Previ
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Radspieler, Alexander. "Untersuchungen zur Synthese von Diazonamid A und Phorbazol A und C." Doctoral thesis, [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=960868712.

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Franke, Jana [Verfasser]. "Totalsynthese von 2-Deshexyl-Thuggacin C und Oxazol-Thuggacin B Derivaten & Studien zur Totalsynthese von aza-Thuggacin / Jana Franke." Hannover : Technische Informationsbibliothek und Universitätsbibliothek Hannover (TIB), 2014. http://d-nb.info/1057897221/34.

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Scholz, Romy. "Synthese der Bacteriocine Amylocyclicin A und Plantazolicin in Bacillus amyloliquefaciens FZB42." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2011. http://dx.doi.org/10.18452/16283.

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Bacillus amyloliquefaciens FZB42 ist ein grampositives Bodenbakterium. Es kann in der Rhizosphäre das Wachstum von Pflanzen fördern und durch die Produktion von Sekundärmetaboliten phytopathogene Organismen hemmen. Aus der Genomanalyse und den dazugehörigen Arbeiten war bekannt, dass Bacillus amyloliquefaciens FZB42 nicht-ribosomal je drei antimikrobielle Polyketide und Lipopeptide herstellt, sowie zwei Siderophore und das Dipeptid Bacilysin. Für Bacillus typische Lantibiotika oder große Bacteriocine wurden nicht gefunden. In dieser Arbeit wird erstmalig gezeigt, dass Bacillus amyloliquefa
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Kalyon, Bahar [Verfasser], Roderich [Akademischer Betreuer] SüßMuth, and Hans-Peter [Akademischer Betreuer] Fiedler. "Fermentation, Isolierung und Strukturaufklärung der ribosomal synthetisierten Thiazol/Oxazol-Peptide Plantazolicin A und B aus Bacillus amyloliquefaciens FZB42 und Strukturaufklärung der Langkocycline aus Streptomyces sp. Acta 3034 / Bahar Kalyon. Gutachter: Roderich Süßmuth ; Hans-Peter Fiedler." Berlin : Technische Universität Berlin, 2014. http://d-nb.info/1067384782/34.

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Linder, Jorg. "Synthesis of the Oxazole-Containing Natural Products Siphonazole and Telomestatin." Thesis, University of Nottingham, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.517791.

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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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Housseman, Christopher. "Synthèse de macrocycles par réaction multi-composants : approche énantiosélective d'une MCR : développement de nouveaux catalyseurs bifonctionnels." Paris 11, 2006. http://www.theses.fr/2006PA112226.

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Books on the topic "Oxazol"

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Palmer, David C., ed. Oxazoles: Synthesis, Reactions, and Spectroscopy. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471649295.

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Trethewey, Andrew Nicholas. Synthesis and evaluation of perhydro-oxazolo [3,4-a] pyridines as fungicides. Portsmouth Polytechnic, 1985.

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Palmer, David C., ed. Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A. John Wiley & Sons, Inc., 2003. http://dx.doi.org/10.1002/0471428035.

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Grünanger, Paolo. Isoxazoles. Wiley, 1991.

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Jones, Gary B. Design, synthesis and evaluation of DNA-binding oxazolo[2,3-c][1,4] benzodiazepines and pyrrolo[2,1-c][1,4] benzodiazepines. Portsmouth Polytechnic, School of Pharmacy and Biomedical Sciences, 1991.

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1957-, Kumar M., and Gupta V. 1966-, eds. Heterocyclic chemistry. Springer, 1998.

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Turchi, I. J. Oxazoles. Wiley & Sons, Incorporated, John, 2009.

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J, Turchi I., ed. Oxazoles. Wiley, 1986.

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Palmer, David C. Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A. Wiley & Sons, Incorporated, John, 2008.

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C, Palmer David, ed. Oxazoles: Synthesis, reactions, and spectroscopy. Wiley, 2003.

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Book chapters on the topic "Oxazol"

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Demaison, J. "269 C3H3NO Oxazole." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_17.

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Li, Jie Jack. "Fischer oxazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_99.

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Li, Jie Jack. "Fischer oxazole synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_107.

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Rauf, Abdul, and Nida Nayyar Farshori. "Oxazoles." In SpringerBriefs in Molecular Science. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_2.

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Mizuno, Tooru M., Ashwini Padhi, Naomi Fineberg, et al. "Oxazolam." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_1742.

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Beyer, Karl-Heinz. "Oxazolam." In Biotransformation der Arzneimittel. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74386-3_237.

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Ware, George W. "Oxamyl." In Reviews of Environmental Contamination and Toxicology. Springer New York, 1988. http://dx.doi.org/10.1007/978-1-4613-8785-5_14.

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Turchi, Ignatius J. "Oxazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187289.ch1.

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Brovarets, V. S., O. P. Mityukhin, A. V. Golovchenko, and B. S. Drach. "Syntheses of Fluorinated 1,3-Oxazoles, 1,3,4-Oxadiazoles, 1,3,4-Thiadiazoles, and Oxazolo[4,5-d]pyrimidines." In ACS Symposium Series. American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1003.ch013.

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Li, Jie Jack. "van Leusen oxazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_259.

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Conference papers on the topic "Oxazol"

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Gašparová, Renata, Eva Haršányiová, and Margita Lácová. "Microwave-assisted reactions of 4-[(4-oxochromen-3-yl)methylene]-2-phenyl-1,3-oxazol-5(4H)-ones with nitrogen bases." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01348.

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Kobayashi, Kaori, and Shozo Tsunekawa. "MICROWAVE SPECTROSCOPY OF OXAZOLE AND ISOXAZOLE." In 74th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.ti07.

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LaVoie, Edmond J., Young Ah Kim, Mavurapu Satyanarayana, et al. "Abstract C76: Oxazole‐containing macrocyles as selective G‐quadruplex stabilizers." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 15-19, 2009; Boston, MA. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/1535-7163.targ-09-c76.

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Oberhauser, B., B. Grohmann, and H. Sperner. "Selective Epimerisation of a Fungal Cyclopeptolide via an 2-Amino-oxazole Intermediate - Conformational Consequences." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01702.

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Kuznetsova, Rimma T., Tat'yana N. Kopylova, K. M. Degtjarenko, et al. "Effect of excitation conditions on photostability of 2-(4pyridyl)-5 phenyl)oxazole laser media." In Second Conference on Pulsed Lasers: Pulsed Atomic and Molecular Transitions, edited by Victor F. Tarasenko, Georgy V. Mayer, and Gueorgii G. Petrash. SPIE, 1995. http://dx.doi.org/10.1117/12.216900.

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Douhal, A., F. Lahmani, A. Zehnacker-Rentien та F. Amat-Guerri. "Ultrafast excited-state H-atom transfer in jet-cooled 2-(2ʹ-hydroxyphenyl)-oxazole derivatives". У The 54th international meeting of physical chemistry: Fast elementary processes in chemical and biological systems. AIP, 1996. http://dx.doi.org/10.1063/1.50150.

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EL Housseiny, Houssein, Suzanne Fery-Forgues, David E. Buso, Marc E. Ternisien, Georges Zissis, and Cédric Renaud. "Use of oxazole-based chromophores as neat films in OLED structures: towards efficient deep-blue emitters." In Organic Photonic Materials and Devices XXIII, edited by Ileana Rau, Okihiro Sugihara, and William M. Shensky. SPIE, 2021. http://dx.doi.org/10.1117/12.2577725.

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Abegão, Luis M. G., Ruben D. Fonseca, Francisco A. Santos, et al. "First Molecular Electronic Hyperpolarizability of Two Oxazoles Dyes in Solution." In Latin America Optics and Photonics Conference. OSA, 2018. http://dx.doi.org/10.1364/laop.2018.th4a.10.

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Park, Wanki, Soon-Chun Chung, So-Hyoung Lee, Jiyoung Park, Chan-Hong Ahn, and Ki-Bong Oh. "Biological Evaluation of marine oxazole-containing macrolides against isocitrate lyase, Na+/ K+ AT Pase, and actin depolymerization." In Annual International Conference on BioInformatics and Computational Biology & Annual International Conference on Advances in Biotechnology. Global Science and Technology Forum, 2011. http://dx.doi.org/10.5176/978-981-08-8119-1_biotech09.

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Guillon, Jean, François Hallé, Solène Savrimoutou, Stéphane Moreau, Daniel-Henri Caignard, and Pascal Sonnet. "Synthesis and Evaluation of New 6-formyl-oxazolo[3,2-a]pyrimidine derivatives as Potential Src Kinase Inhibitors." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05566.

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