Relevant bibliographies by topics / Phenylthiazoyl

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

Academic literature on the topic 'Phenylthiazoyl'

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

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Journal articles on the topic "Phenylthiazoyl"

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Mamedov, Vakhid A., Yakov A. Levin, Evgeniya K. Trutneva, et al. "Functionalized 4-methyl-5-phenylthiazole and 1,3-bis(4'-methyl-5'-phenylthiazol-2'-yl)benzene. Approaching thiazole macrocycles." Arkivoc 2004, no. 12 (2005): 47–69. http://dx.doi.org/10.3998/ark.5550190.0005.c06.

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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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Sarangi, P. K. N., J. Sahoo, S. K. Paidesetty, and G. P. Mohanta. "SYNTHESIS, SPECTRAL CHARACTERIZATION AND ANTICANCER EVALUATION OF NEW DIAZENYL SCHIFF BASE DERIVATIVES." INDIAN DRUGS 54, no. 02 (2017): 20–28. http://dx.doi.org/10.53879/id.54.02.10877.

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A series of several diazenyl Schiff base derivatives were designed and synthesized through azo coupling of diazotised primary amines with the novel synthesized Schiff base ligand (E)-N-((2-chloroquinolin-3-yl) methylene)-4-phenylthiazol-2-amine. All the synthesized compounds have been analysed by different spectral techniques such as elemental analysis, 1H NMR, FT-IR, UV-Vis and LC-MS for their structural confirmation. The above conjugates have been studied for their solvent effects by treating them with different solvents. The results of in vitro cytotoxic study of the synthesized compounds a
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Abdel-Wahab, Bakr F., Benson M. Kariuki, Hanan A. Mohamed, and Gamal A. El-Hiti. "Catalyst-Free Synthesis of Novel 4-(Benzofuran-2-yl)-N-phenylthiazol-2(3H)-imines, Crystal Structure Elucidation, and the Effect of Phenyl Substitution on Crystal Packing." Crystals 13, no. 8 (2023): 1239. http://dx.doi.org/10.3390/cryst13081239.

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A one-pot reaction of an equimolar mixture of 4-methoxyaniline, phenyl isothiocyanate, and 2-bromoacetylbenzofuran in absolute ethanol in the absence of any catalysts afforded 4-(benzofuran-2-yl)-3-(4-methoxyphenyl)-N-phenylthiazol-2(3H)-imine with an 83% yield. Under similar conditions, 4-flouroaniline provided a mixture of the expected 4-(benzofuran-2-yl)-3-(4-fluorophenyl)-N-phenylthiazol-2(3H)-imine and unexpected 4-(benzofuran-2-yl)-N-(4-fluorophenyl)-3-phenylthiazol-2(3H)-imine at an overall 73% yield. The structures of the synthesized heterocycles were confirmed using NMR spectroscopy.
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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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Luo, Yong, Yongxia Zhu, Kai Ran, et al. "Synthesis and biological evaluation of N-(4-phenylthiazol-2-yl)cinnamamide derivatives as novel potential anti-tumor agents." MedChemComm 6, no. 6 (2015): 1036–42. http://dx.doi.org/10.1039/c4md00573b.

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Luo, Yong, Yongxia Zhu, Kai Ran, et al. "Correction: Synthesis and biological evaluation of N-(4-phenylthiazol-2-yl)cinnamamide derivatives as novel potential anti-tumor agents." MedChemComm 6, no. 7 (2015): 1404. http://dx.doi.org/10.1039/c5md90027a.

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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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Dissertations / Theses on the topic "Phenylthiazoyl"

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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 "Phenylthiazoyl"

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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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Amose, Yardily, Fathima Shahana, and Abbs Fen Reji. "Density Functional Theory and Molecular Modeling of the Compound 2-[2-(4-Methylphenylamino)-4-phenylthiazol-5-yl]benzofuran." In Furan Derivatives - Recent Advances and Applications. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.99577.

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The compound 2-[2-(4-methylphenylamino)-4-phenylthiazol-5-yl]benzofuran was prepared from 1-(4-methylphenyl)-3-(N-phenylbenzimidoyl)thiourea and 2-(2-bromoacetyl) benzofuran in the presence of triethylamine and characterized by FTIR, NMR, and mass spectra. Density functional theory (DFT) computations were adopted for the geometry optimization of this compound, to evaluate their Mulliken atomic charge distribution, HOMO-LUMO energy gap, and vibrational analysis. The titled compound induced G1 cell cycle arrest, which is regulated by CDK2 in cancer cells. Therefore, we used molecular modeling to
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Conference papers on the topic "Phenylthiazoyl"

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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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