Relevant bibliographies by topics / Thiazol

Contents

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

Academic literature on the topic 'Thiazol'

Author: Grafiati
Published: 4 June 2021
Last updated: 31 July 2024

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Journal articles on the topic "Thiazol"

1

Borde, Ramesh M., Satish B Jadhav, Rahul R Dhavse, and Achut S Munde. "DESIGN, SYNTHESIS, AND PHARMACOLOGICAL EVALUATION OF SOME NOVEL BIS-THIAZOLE DERIVATIVES." Asian Journal of Pharmaceutical and Clinical Research 11, no. 4 (2018): 164. http://dx.doi.org/10.22159/ajpcr.2018.v11i4.23413.

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Objective: A series of substituted 5,2-bis-thiazoles derivatives were synthesized by Hantzsch reaction and evaluated in vitro for antimicrobial activity against Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, and Staphylococcus aureus. Methods: 2-(4-(benzyloxy)phenyl)-4-methylthiazole-5-carbothioamide were synthesized and allowed to react with various α-haloketones to give 5,2-bis-thiazoles, i.e., 2-(4-(benzyloxy)phenyl)-4-methyl-5-(4-substituted thiazol-2-yl)thiazole derivatives in excellent yield. The synthesized compounds were characterized by spectroscopic methods as well as e
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Turov, Kostyantyn. "Anticancer evaluation of di- and trifunctional substituted 1,3-thiazoles." Ukr. Bioorg. Acta 2020, Vol. 15, N1 15, no. 1 (2020): 2–11. http://dx.doi.org/10.15407/bioorganica2020.01.002.

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Anticancer activity of a series of polyfunctional substituted 1,3-thiazoles has been studied within the international scientific program “NCI-60 Human Tumor Cell Lines Screen”. Screening was performed in vitro on 60 cell lines of lungs, kidneys, CNS, ovaries, prostate, and breast cancer, epithelial cancer, leukemia, and melanoma. The most effective compounds were those with a piperazine substituent at C2 of the 1,3-thiazole cycle: 1-(4-((4-methylphenyl)-sulfonyl)-2-phenyl-1,3-thiazol-5-yl)piperazine (average lg GI50 = -5.87, lg TGI = -5.54, lg LC50 = -5.21), 1-(2-(3,5-dimethyl-1H-pyrazol-1-yl)
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Dekate, Shital M., Kishor M. Hatzade, and Ajay M. Ghatole. "A Facile Synthesis of Thiazole Derivatives bearing Imidazole Moiety, Schiff Bases and their O-Glucosides." Asian Journal of Chemistry 35, no. 1 (2022): 29–38. http://dx.doi.org/10.14233/ajchem.2023.24049.

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A unique approach for the synthesis of new thiazole O-glycosides is presented in this work. 2-Amino-4-hydroxy-phenyl-1,3-thiazole-5-carboxaldehyde (3a) was reacted with phenyl glyoxal and benzil to form 4-(4-hydroxy-phenyl)-5-(4-phenyl-1H-imidazol-2-yl)-thiazol-2-amine (4a) and 4-(4-hydroxy-phenyl)-5-(4,5-diphenyl-1H-imidazol-2-yl)-thiazol-2-amine (4b), respectively. A series of substituted Schiff bases of 4a and 4b were synthesized reacting with various aryl aldehyde to form 2-(imino substituted benzal)-4-(4-hydroxy-phenyl)-5-(4-phenyl-1H-imidazol-2-yl)-thiazoles (5a-e) and 2-(imino substitut
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Dawane, Bhaskar Sadashiv. "Design, synthesis and evaluation of novel 3-(substitutedphenyl)-2-(4-(substitutedphenyl) thiazol-2-yl)-2hpyrazolo [3, 4-d] thiazol-5(6h)-one derivatives as anti-breast cancer agents." Journal of medical pharmaceutical and allied sciences 11, no. 6 (2022): 5453–60. http://dx.doi.org/10.55522/jmpas.v11i6.4475.

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Mainstream cancer research has continued to place a significant emphasis on the development of new and effective therapeutic candidates to tackle rising treatment resistance and off-target toxicities. Here, a series of novel 3-(substitutedphenyl)-2-(4-(substitutedphenyl)thiazol-2-yl)-2Hpyrazolo[3,4-d]thiazol-5(6H)-one derivatives were synthesized and characterized. The ability of the synthesized compounds to reduce the survival of the human breast cancer cell line MDA-MB 231 was evaluated. When compared to the reference chemical, 5-fluorouracil, 3-(4-chlorophenyl)-2-(4- (4-chlorophenyl)thiazol
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Mishchenko, Mariia, Sergiy Shtrygol, Danylo Kaminskyy, and Roman Lesyk. "Thiazole-Bearing 4-Thiazolidinones as New Anticonvulsant Agents." Scientia Pharmaceutica 88, no. 1 (2020): 16. http://dx.doi.org/10.3390/scipharm88010016.

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Here, we describe the synthesis and anticonvulsant activity of thiazole-bearing hybrids based on 2-imino-4-thiazolidinone and 2,4-dioxothiazolidine-5-carboxylic acid cores. The structure of target compounds was based on the following: (i) A combination of two thiazole cores; (ii) similarity to ralitolin’s structure; (iii) the compliance with structural requirements for the new anticonvulsants. Target compounds were synthesized via known approaches based on Knoenavegel reaction, alkylation reaction, and one-pot three-component reaction. Anticonvulsant properties of compounds were evaluated in t
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Rayala, Ramanjaneyulu, Prakash Chaudhari, Ashley Bunnell, Bracken Roberts, Debopam Chakrabarti, and Adel Nefzi. "Parallel Synthesis of Piperazine Tethered Thiazole Compounds with Antiplasmodial Activity." International Journal of Molecular Sciences 24, no. 24 (2023): 17414. http://dx.doi.org/10.3390/ijms242417414.

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Thiazole and piperazine are two important heterocyclic rings that play a prominent role in nature and have a broad range of applications in agricultural and medicinal chemistry. Herein, we report the parallel synthesis of a library of diverse piperazine-tethered thiazole compounds. The reaction of piperazine with newly generated 4-chloromethyl-2-amino thiazoles led to the desired piperazine thiazole compounds with high purities and good overall yields. Using a variety of commercially available carboxylic acids, the parallel synthesis of a variety of disubstituted 4-(piperazin-1-ylmethyl)thiazo
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Walmik, Prabhakar, Basavaraj S. Naraboli, Swathi B, and Somashekhar Ghanti. "DESIGN, SYNTHESIS OF BIOLOGICALLY ACTIVE HETEROCYCLES CONTAINING INDOL- THIAZOLYL- THIAZOLIDINONE DERIVATIVES." Asian Journal of Pharmaceutical and Clinical Research 11, no. 3 (2018): 113. http://dx.doi.org/10.22159/ajpcr.2018.v11i3.22199.

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Objective: The present study envisage a novel series of thiazole, indole and thiazolidine derivatives, namely, N-((5-Substituted-2-phenyl-1 H-indol-3-yl)methylene)-4,5,6,7-tetrahydro-5,7,-dimethylbenzo [d]thiazole-2-amine (4a-c), 2-(5-substituted-2-phenyl-1H-indol-3-yl)-3-(4,5,6,7- trimethylbenzo[d]thiazol-2-yl)-thiazolidin-4-one (5a-c) and 5-benzylidine-2-(5-substituted-2phenyl-1H-indol-3yl)-3-(4,5,6,7-tetrahydro-5,5,7- trimethylbenzo[d]thiazol-2-yl) thiazolidin-4-one (6a-c).Methods: All the newly synthesized compounds were characterized by infrared, 1H, 13C nuclear magnetic resonance and mas
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Abu-Melha, Sraa. "Synthesis, Modeling Study and Antioxidants Activity of New Heterocycles Derived from 4-Antipyrinyl-2-Chloroacetamidothiazoles." Applied Sciences 8, no. 11 (2018): 2128. http://dx.doi.org/10.3390/app8112128.

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The present work reports the preparation of twelve new heterocyclic scaffolds containing an antipyrinyl-thiazole hybrid through the reaction of 4-antipyrinyl-2-chloroacetamido-thiazoles 1 and 6 with various types of nucleophiles, namely; ethyl thioglycolate, 2-mercaptobenzothiazole, 2-mercaptobenzoxazole, ammonium thiocyanate, malononitrile, and salicylaldehyde. The constructed compounds were characterized by conventional spectroscopic techniques (IR, 1H NMR, 13C NMR, and mass analysis). A DFT method (material studio package) was used to predict the geometry, bond lengths, bond angles, and dip
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Kabra, Vijaya, Neelima Gupta, Sama Jain, and Varsha Saxena. "Pyrimidin-/thiazol-/thiazolin-ylidenamidothiophosphoric dichlorides." Heteroatom Chemistry 14, no. 6 (2003): 498–502. http://dx.doi.org/10.1002/hc.10170.

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Sonparote, P. M., and D. M. Chavhan. "Convenient Method for Synthesis of New Derivatives of (1-(4-(2,4-dichlorophenyl)-2-((4-nitrobenzylidene) amino)thiazol-5-yl)ethan-1-one." International Research Journal of Pure and Applied Chemistry 24, no. 5 (2023): 139–44. http://dx.doi.org/10.9734/irjpac/2023/v24i5833.

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The new derivatives of thiazole based Schiff base of (1-(5-(2,3,4-trisubstitutedphenyl)-2-((4-nitrobenzylidene)amino)thiazol-4-yl)ethan-1-one (6) were synthesized by the treatment of 1-(2-amino-5-(2,3,4-trisubstitutedphenyl)thiazol-4-yl)ethan-1-one (4) and corresponding substituted benzaldehyde (5) in low cost easily available non flammable stable and ecofriendly solvent Polyethylene glycol-400 solvent medium. The reactions were performed in the good yield and less time. The structures of all synthesized compounds were established on the basis of elemental analysis, IR, NMR and Mass spectral d
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Dissertations / Theses on the topic "Thiazol"

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Jobard-Rouppert, Fabienne. "Deux-(thiazol-5-yloxy)éthylamines et 3-(4-arylpipérazin-yl)-1-(thiazol-5-yloxy)propan-2-ols : synthèse et évaluation pharmacologique." Nantes, 1993. http://www.theses.fr/1993NANT07VS.

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Ghewa, El Achkar. "Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2." Thesis, Paris Est, 2015. http://www.theses.fr/2015PESC0033.

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Les statines sont des inhibiteurs sélectifs de la 3-hydroxy-3-méthylglutaryl-coenzyme A réductase, utilisées pour diminuer la biosynthèse du cholestérol. Ces molécules possèdent en plus de leur capacité à réduire le cholestérol des effets pléiotropiques comme les propriétés anti-inflammatoires et anti-oxydantes. Les cucurbitacines sont des triterpènes dérivés des plantes, ayant des propriétés biologiques diverses comme les effets anti-inflammatoires et anticancéreux, associées toutefois à une toxicité élevée. Les dérivés de thiazole sont des molécules contenant un noyau hétérocyclique formé de
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Leopold, Hendrik [Verfasser]. "Cyclometallierte Übergangsmetall Thiazol-2-yliden-Carbenkomplexe: Phosphoreszente Emitter für OLEDs / Hendrik Leopold." München : Verlag Dr. Hut, 2016. http://d-nb.info/1122524641/34.

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McLachlan, Janice. "Synthesis of 2-amino-4-(thiazol-5-yl) pyrimidines as potential kinase inhibitors." Thesis, University of Edinburgh, 2006. http://hdl.handle.net/1842/12637.

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Herb, Monika [Verfasser], and Tanja [Akademischer Betreuer] Schirmeister. "Synthese von Pyridin-, Pyridylessigsäure- und Thiazol-Derivaten als potentielle Inhibitoren der SARS-CoV-Mpro / Monika Herb. Betreuer: Tanja Schirmeister." Würzburg : Universitätsbibliothek der Universität Würzburg, 2011. http://d-nb.info/1018163344/34.

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Barzen, Sebastian [Verfasser], Holger [Akademischer Betreuer] Stark, and Dieter [Akademischer Betreuer] Steinhilber. "Synthese und Charakterisierung von Inhibitoren der 5-Lipoxygenase mit Thiazol-Grundgerüst / Sebastian Barzen. Gutachter: Holger Stark ; Dieter Steinhilber. Betreuer: Holger Stark." Frankfurt am Main : Univ.-Bibliothek Frankfurt am Main, 2012. http://d-nb.info/1044093900/34.

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Dannenbauer, Nicole [Verfasser], and Klaus [Gutachter] Müller-Buschbaum. "Koordinationspolymere und -verbindungen mit intrinsischer Lumineszenz auf Basis von Selten-Erd-Chloriden, Thiazol, Thiolaten und Amin-Co-Liganden / Nicole Dannenbauer. Gutachter: Klaus Müller-Buschbaum." Würzburg : Universität Würzburg, 2016. http://d-nb.info/1112041486/34.

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ALIANÇA, Amanda Silva dos Santos. "Atividade biológico de compostos ftalimido-Tiazóis sobre Leishmania infantum (Nicolle, 1908)." Universidade Federal de Pernambuco, 2016. https://repositorio.ufpe.br/handle/123456789/17557.

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Schöffler, Anne [Verfasser], and Bernd Franz [Akademischer Betreuer] Straub. "Entwicklung hochaktiver, dinuklearer NHC-Kupfer(I)katalysatoren auf Thiazol-, Xanthin- und 1,2,3-Triazol-Basis für Azid-Alkin-Cycloadditionen / Anne Lisa Schöffler ; Betreuer: Bernd F. Straub." Heidelberg : Universitätsbibliothek Heidelberg, 2020. http://d-nb.info/1218599383/34.

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Schöffler, Anne Lisa [Verfasser], and Bernd F. [Akademischer Betreuer] Straub. "Entwicklung hochaktiver, dinuklearer NHC-Kupfer(I)katalysatoren auf Thiazol-, Xanthin- und 1,2,3-Triazol-Basis für Azid-Alkin-Cycloadditionen / Anne Lisa Schöffler ; Betreuer: Bernd F. Straub." Heidelberg : Universitätsbibliothek Heidelberg, 2020. http://d-nb.info/1218599383/34.

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Books on the topic "Thiazol"

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Geōrgousopoulos, Kōstas. Thiasos poikiliōn. Ekdoseis Kastaniōtē, 1993.

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Papageōrgiou, Gēsēs. Ho megalos thiasos. Ekdoseis Astraia, 2000.

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Kathrin, Fuchs, Tsoukker Larissa, and Gluck50 (Gallery), eds. Thiago Rocha Pitta. Mousse Publishing, 2013.

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Phakinos, Michalēs. Ephēmereuōn thiasos: Kai alles histories. Ekdoseis Kastaniōtē, 1989.

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Melo, Thiago Martins de, and Samantha Moreira. Thiago Martins de Melo. Capivara Contemporânea, 2019.

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Sowoidnich, Werner. Neue Chelate der Benzthiazol- und Benzobisthiazolreihe: Darstellung und spektroskopische Eigenschaften. Hartung-Gorre, 1989.

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Frederico, Krüger Marcos, ed. Thiago de Mello: Melhores poemas. Global Editora, 2009.

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Francesco, Galli, Lorenzoni Franco 1953-, and Ferri Francesca, eds. Un teatro nel paesaggio: Fotografare O Thiasos TeatroNatura. Titivillus, 2007.

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Jenny, Christian-Johannes. Synthese und Reaktionen von 2-Thiazolin-5-thionen. [s.n.], 1986.

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Pitta, Thiago Rocha. Thiago Rocha Pitta: Notas de um desabamento. Escola de Artes Visuais do Parque Lage - EAV, 2010.

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Book chapters on the topic "Thiazol"

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Kumar Pandey, Anoop, Ankit Kumar Sharma, V. K. Singh, Benard S. Mwankemwa, and Vijay Singh. "Geometry vibrational and NBO analysis of thiazole derivative (Z)-4-{[4-(3-methyl3-phenylcyclobutyl)thiazol-2-yl]amino}-4-oxobut-2-enoic acid." In Emerging Trends in IoT and Computing Technologies. Routledge, 2023. http://dx.doi.org/10.1201/9781003350057-53.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with (2-methoxycarbonylmethylimino)-5-methyl-thiazol-3-yl)acetic acid." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_243.

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Kaur, Navjeet. "Thiazole Synthesis." In Lawesson’s Reagent in Heterocycle Synthesis. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4655-3_2.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with (2-methoxycarbonyl-methylimino)-5-methyl-thiazol-3-yl)-acetic acid and pyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_304.

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Rauf, Abdul, and Nida Nayyar Farshori. "Thiazoles." In SpringerBriefs in Molecular Science. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_3.

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Demaison, J. "272 C3H3NS Thiazole." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_20.

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Li, Jie Jack. "Cook-Heilbron thiazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_66.

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Begtrup, Mikael, and Christian Roussel. "Mesoionic Thiazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187074.ch1.

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Winkelmann, Jochen. "Self-diffusion coefficient of thiazole." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_76.

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Metzger, Jacques V., Emile-Jean Vincent, Jacques Chouteau, and Gilbert Mille. "Properties and Reactions of Thiazole." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187081.ch2.

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Conference papers on the topic "Thiazol"

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Ustinov, Ilya, Nikolaj Khlytin, Yurij Atroshchenko, and Irina Shahkeldyan. "NEW THIAZOL DERIVATIVES CONTAINING NITRO QUINOLINE FRAGMENT." In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m797.aks-2019/383-384.

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Pshigonova, Emilia B., Polina O. Suntsova, Aleksey A. Gagarin, Alexandr L. Shlyapnikov, and Nataliya P. Belskaya. "3-(4-hydroxyphenyl)-2-(thiazol-2-yl)acrylonitriles: Synthesis, chemical and photophysical properties." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0068951.

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Kammel, Richard. "Synthesis of Substitued 5-(2-Hydroxyphenyl)-1,3-Thiazol-4-Oles AS pH Switchable Fluorophores." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a009.

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Joy, Muthipeedika Nibin, Rishikesan Rathnasamy, Ranjith P. Karuvalam, et al. "An efficient RP-HPLC method for UV/mass triggered purification of bis-thiazol-2-amine derivatives." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069241.

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Moses, Liji E., S. Pari, B. Kunhanna Sarojini, Krishnakishore Majalakere, and Issac Hubert Joe. "Z-scan study of a novel optical limiter N-(3,4-dichlorophenyl)-4-(4-chlorophenyl)-1,3-thiazol-2-amine." In 2ND INTERNATIONAL CONFERENCE ON MATERIALS FOR ENERGY AND ENVIRONMENT 2020. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0141623.

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Moses, Liji E., S. Pari, Isaac Hubert Joe, B. Kunhanna Sarojini, and Krishnakishore Majalakere. "Spectroscopic, DFT and Z-scan assisted study of an azo compound N-(2,6-dimethylphenyl)-4-(4-chlorophenyl) thiazol-2-amine." In 2ND INTERNATIONAL CONFERENCE ON MATERIALS FOR ENERGY AND ENVIRONMENT 2020. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0141624.

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Al-Yousefi, Dalal Abbas, and Ibtehaj Raheem Ali. "Spectrophotometric determination of transition elements by cloud point extraction with use laboratory by thiazol azo reagent and applied in environmental samples." In 3RD INTERNATIONAL SCIENTIFIC CONFERENCE OF ALKAFEEL UNIVERSITY (ISCKU 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0067206.

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Váry, Tomáš, Zita Tokárová, and Vojtech Nádaždy. "Energy resolved electrochemical impedance spectroscopy of furan-substitued thiazolo [5,4-d]thiazoles." In APPLIED PHYSICS OF CONDENSED MATTER (APCOM 2021). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0067189.

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Zhang, Weiyi, Gang Zhou, and Zhong-Sheng Wang. "Thiazolo[5,4-d]thiazole-Based Organic Dyes for Quasi-Solid-State Dye-Sensitized Solar Cells." In Advanced Optoelectronics for Energy and Environment. OSA, 2013. http://dx.doi.org/10.1364/aoee.2013.asa3a.12.

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Ali, Marwa Salem, and Ibtehaj Raheem Ali. "Preparation and characterization of new reagent derivative of thiazol azo for spectral evaluation of some metal elements in different samples using cloud point technique." In 3RD INTERNATIONAL SCIENTIFIC CONFERENCE OF ALKAFEEL UNIVERSITY (ISCKU 2021). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0067208.

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