Relevant bibliographies by topics / Phenylthiazole

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

Academic literature on the topic 'Phenylthiazole'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Phenylthiazole"

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Bhuiyan, M. H., and A. F. M. H. Rahman. "Synthesis and Antimicrobial Evaluation of Some Thiazole Derivatives." Journal of Scientific Research 3, no. 1 (2010): 111. http://dx.doi.org/10.3329/jsr.v3i1.5419.

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Reaction of 2-amino-4-phenylthiazole with various aromatic aldehydes afforded 2-arylideneamino-4-phenylthiazoles. On the other hand treatment of 2-amino-4-phenylthiazole with several acyl halides furnished N-(thiazol-2-yl)-amides. The synthesized compounds have been screened for their antimicrobial activity against Bacillus cereus, Bacillus subtilis, Staphylococcus aureus, Shigella dysenteriae, Salmonella typhi, Pseudomonous sp. bacteria and Aspergillus niger, Penicillium notatum, Aspergillus funiculosus, Collectrichum corchori Ikata (Yoshida) and Curvularia lunata fungi respectively. Some of
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Fouda, Abdel Aziz, A. Abdel Nazeerb, and K. M. Abdel Khalek. "Corrosion Inhibition of Zinc Using Some Phenylthiazole Derivatives in Hydrochloric acid Solutions." JOURNAL OF ADVANCES IN CHEMISTRY 12, no. 7 (2013): 425–40. http://dx.doi.org/10.24297/jac.v12i7.2798.

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The inhibitive action of some phenylthiazole derivatives namely: 2-acetylamino-5-p-bromophenylazo-4-phenylthiazole (BPT), 2-acetylamino-5-p-methylphenylazo-4-phenylthiazole (MPT), 2-acetylamino-5-p-methoxyphenylazo-4-phenylthiazole (XPT) and 2-acetylamino-5-p-nitrophenylazo-4-phenylthiazole (NPT), on zinc corrosion in 0.2 M HCl has been studied using weight loss, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS)and electrochemical frequency modulation (EFM) measurements. The results showed that the dissolution rate of zinc decreases with increasing the phenylthiazole d
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Fouda, Abdel Aziz, A. Abdel Nazeerb, and K. M. Abdel Khalek. "Corrosion Inhibition of Zinc Using Some Phenylthiazole Derivatives in Hydrochloric acid Solutions." JOURNAL OF ADVANCES IN CHEMISTRY 4, no. 2 (2008): 425–40. http://dx.doi.org/10.24297/jac.v4i2.2704.

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The inhibitive action of some phenylthiazole derivatives namely: 2-acetylamino-5-p-bromophenylazo-4-phenylthiazole (BPT), 2-acetylamino-5-p-methylphenylazo-4-phenylthiazole (MPT), 2-acetylamino-5-p-methoxyphenylazo-4-phenylthiazole (XPT) and 2-acetylamino-5-p-nitrophenylazo-4-phenylthiazole (NPT), on zinc corrosion in 0.2 M HCl has been studied using weight loss, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS)and electrochemical frequency modulation (EFM) measurements. The results showed that the dissolution rate of zinc decreases with increasing the phenylthiazole d
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Zhu, ShaoPing, Yuan Chen, Jun Sun, YuTing Yang, and ChuanJun Yue. "Synthesis, Characterization, Thermochromism, and Photochromism of Aromatic Aldehyde Hydrazone Derivatives." Journal of Chemistry 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/8460462.

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The Schiff bases N-(5-phenylthiazole-2-yl)-2-hydroxylnaphthaldehydehydrazone (1), N-(4′-chloro-5-phenylthiazole-2-yl)-2-hydroxylnaphthaldehydehydrazone (2), and N-(4′-nitro-5-phenylthiazole-2-yl)-2-hydroxylnaphthaldehydehydrazone (3) were synthesized. These compounds were characterized by using IR,1H NMR,13C NMR, and MS. The photochromism of the compounds was investigated by IR and UV-visible spectrometry which is time variable under irradiation of 254 nm UV light. The thermochromism of the compounds was studied using temperature-variable IR, UV-visible spectrometry, TG, and differential scann
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Au-Alvarez, O., R. C. Peterson, A. Acosta Crespo, et al. "2-Amino-4-phenylthiazole." Acta Crystallographica Section C Crystal Structure Communications 55, no. 5 (1999): 821–23. http://dx.doi.org/10.1107/s0108270199001961.

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Stokes, Emily C., Emily E. Langdon-Jones, Lara M. Groves, et al. "Cationic, luminescent cyclometalated iridium(iii) complexes based on substituted 2-phenylthiazole ligands." Dalton Transactions 44, no. 18 (2015): 8488–96. http://dx.doi.org/10.1039/c4dt03054k.

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D., C. DASH, K. BEHERA R., M. SEN (Miss), and M. MEHER F. "Synthesis and Characterisation of some Transition Metal Complexes of 4-Substituted-2-thiazolylhydrazones of Salicylaldehyde and 2-Hydroxyacetophenone." Journal of Indian Chemical Society Vol. 68, Dec 1991 (1991): 663–64. https://doi.org/10.5281/zenodo.6134555.

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Post-Graduate Department of Chemistry, Sambalpur University, Jyoti Vihar, Burla-788 019 <em>Manuscript received 27 April 1988, revised 21 November 1991, accepted 6 December 1991</em> THE communication reports the synthesis and structural studies on the complexes of Co<sup>II</sup>, Ni<sup>II</sup> and Cu<sup>ll</sup> with some hydrazone derivatives containing thiazole moiety and a OH group near the condensation site, such as 2-salicylideneiminoamino-4- phenylthiazole (SPTH), 2-salicylideneiminoamino-4-bromophenylthiazole (SBPTH), 2-&alpha;-methylsalicyli-deneiminoamino-4- phenylthiazole (MSPTH
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Zhao, Jiang, Xiaojie Chen, Jianglan Wu, Maoyang Jian, Guijiang Zhou, and Zhenguo Chi. "Fluoro-benzenesulfonyl-functionalized 2-phenylthiazole-type iridium(iii) complexes for efficient solution-processed organic light-emitting diodes." Journal of Materials Chemistry C 8, no. 30 (2020): 10390–400. http://dx.doi.org/10.1039/d0tc02250k.

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Bhuiyan, Md Mosharef Hossain, Mohammed M. Matin, AFM Hafizur Rahman, and Md Rabiul Alam. "Synthesis and Biological Evaluation of Sugar Induced Thiazole Derivatives." Chittagong University Journal of Science 41, no. 1 (2021): 68–84. http://dx.doi.org/10.3329/cujs.v41i1.51915.

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The starting materials, 2-amino-4-phenylthiazole and 2-amino-4,5,6,7-tetrahydrobenzo[d]thiazole, were prepared by reacting thiourea with acetophenone and cyclohexanone in the presence of iodine under heating on a water bath with occasional stirring, respectively. Reaction of 2-amino-4-phenylthiazole and 2-amino-4,5,6,7-tetrahydrobenzo[d]thiazole with various sugars afforded corresponding N-glycoside derivatives in good yields. The structures of the synthesized N-glycosides derivatives have been established on the basis of their IR and NMR spectral data. The obtained compounds were screened for
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Mayhoub, Abdelrahman S., Mansoora Khaliq, Carolyn Botting, Ze Li, Richard J. Kuhn, and Mark Cushman. "An investigation of phenylthiazole antiflaviviral agents." Bioorganic & Medicinal Chemistry 19, no. 12 (2011): 3845–54. http://dx.doi.org/10.1016/j.bmc.2011.04.041.

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Dissertations / Theses on the topic "Phenylthiazole"

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Millet, Antoine. "Synthèse et optimisation de nouveaux dérivés anti-mélanome 4-phényl-2-aminothiazole ciblant GRP78 pour contourner les mécanismes de résistances." Thesis, Université Côte d'Azur (ComUE), 2016. http://www.theses.fr/2016AZUR4084.

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Depuis 2011, pas moins de 7 nouvelles thérapies ont été acceptées pour le traitement du mélanome métastatique. Ces nouvelles thérapies, composées de 4 inhibiteurs de B-Raf et MEK et de 3 anticorps, ont amélioré significativement la durée de vie des patients. Néanmoins, la forme résistante de la maladie est toujours problématique et aucun traitement à l’heure actuelle ne permet d’éradiquer la maladie. Dans ce contexte, ces travaux présentent la synthèse et la caractérisation de nouveaux dérivés 4-phényl-2-aminothiazole, actifs contre les formes résistantes du mélanome. 3 points structuraux clés
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Book chapters on the topic "Phenylthiazole"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with Schiff-base derived from 4-phenylthiazole-2-semicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_251.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with Schiff-base derived from 4-phenylthiazole-2-semicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_252.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with Schiff-base derived from 4-phenylthiazole-2-semicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 3. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62470-8_250.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base derived from 4-phenylthiazole-2-semicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_527.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base derived from 4-phenylthiazole-2-semicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_529.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with Schiff-base derived from 4-phenylthiazole-2-semicarbazide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 4. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62474-6_528.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis[3-(4′-phenylthiazole-2′-yl)-1-(2′-hydroxy-1′-iminomethyl)phenylurea]cobalt(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_409.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis[3-(4′-phenylthiazole-2′-yl)-1-(2′,4′-dihydroxy-1′-iminomethyl)phenylurea]cobalt(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_410.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis[3-(4′-phenylthiazole-2′-yl)-1-(2′,-hydroxy-5′-chloro-1′-iminomethyl)phenylurea]cobalt(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_411.

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Stolowitz, Mark L., Chin-Sook Kim, Steven R. Marsh, and Leroy Hood. "Thiobenzoylation Method of Protein Sequencing: Gas Chromatography/Mass Spectrometric Detection of 5-Acetoxy-2-Phenylthiazoles." In Methods in Protein Sequence Analysis. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4899-1603-7_5.

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Conference papers on the topic "Phenylthiazole"

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Stojković, Danijela Lj, Verica V. Jevtić, Đorđe S. Petrović, et al. "SYNTHESIS AND CHARACTERIZATION OF PLATINUM(II/IV) COMPLEXES WITH 2-AMINO-5-METHYL-4-PHENYLTHIAZOLE." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.339s.

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This paper examines the synthesis of two new complexes of platinum(II/IV) ion, general formula [PtL2]Cl2 and [PtL2]Cl4, where L is 2-amino-5-methyl-4-phenylthiazole. The structures of the above mentioned compounds were determined by elemental microanalysis, infrared, 1H and 13C NMR spectroscopy.
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