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Relevant bibliographies by topics / Thiazolyl substituted Schiff's bases

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Academic literature on the topic 'Thiazolyl substituted Schiff's bases'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Thiazolyl substituted Schiff's bases"

1

R., S. Talegaonkar, and S. Burghate A. "pH-metric studies on formation constants of the complexes of substituted thiazolyl Schiff's bases with some lanthanide metal ions." Journal of Indian Chemical Society Vol. 89, Nov 2012 (2012): 1585–89. https://doi.org/10.5281/zenodo.5771932.

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Post Graduate Department of Chemistry, Shri Shivaji Science College, Amravati-444 603, Maharashtra, India <em>E-mail</em> : rupaliyeotikar@gmail.com Manuscript received 22 September 2011, revised 08 February 2012, accepted 09 February 2012 The stability constants of the complexes of La<sup>llI</sup>, Pr<sup>lll</sup> and Sm<sup>III</sup> with 2-[3-(4-methoxy-phenyl)-1-(4-phenyl-thiazol-2-yllmino )-allyl]-4-methyl phenol, 2-[3-pheny 1-1-( 4-pheny 1-thiazol-2-ylim ino )-allyl]-4-methy 1-phenol and 2-[3-( 4- chlorophenyl)-1-(4-phenyl-thiazol-2-ylimino)-allyl]-4-methyl-phenol have been determined

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2

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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3

Aleqsanyan, I. L., and L. P. Hambardzumyan. "Synthesis of Schiff Bases and Isoindolyl- and Thiazolyl-Substituted Quinolines from 6-Amino-2-methylquinolin-4-ol." Russian Journal of Organic Chemistry 58, no. 10 (2022): 1434–37. http://dx.doi.org/10.1134/s1070428022100086.

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4

Veerabhadraiah, Udarapu, Vedeela Rajeswar Rao, and Tadepalcy Venkata Padmanabha Rao. "Reaction of mercaptoacetic acid and chloroacetyl chloride with benzalamino thiazolyl coumarins." Collection of Czechoslovak Chemical Communications 55, no. 2 (1990): 535–39. http://dx.doi.org/10.1135/cccc19900535.

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2-Aryl-3-[4-(2-oxo-2H-1-benzopyran-3-yl)-2-thiazolyl]-4-thiazolidinones (III), have been synthesized by the reaction of Schiff's bases (II) derived from 3-(2-amino-4-thiazolyl)-2H-1-benzopyran-2-ones (I) with mercaptoacetic acid. The Schiff's bases on reaction with chloroacetyl chloride in the presence of triethylamine in dioxane gave chloroacetamido derivative (IV) instead of expected compound V.

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5

P. Kavitha and N. Vijayakumari. "SYNTHESIS AND CHARACTERIZATION OF BENZOTHIAZOLE SCHIFF BASES BASED METAL COMPLEXES AND THEIR BIOLOGICAL APPLICATIONS." RASAYAN Journal of Chemistry 18, no. 02 (2025): 1170–76. https://doi.org/10.31788/rjc.2025.1829261.

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A new benzothiazole Schiff base ligand named (E)-N-(6-((2-hydroxy-5-methylbenzylidene)amino)benzo[d]thiazol-2- yl)cyclohexane-carboxamide (BSB) was prepared through the condensation reaction of N-(6-aminobenzo[d]thiazol2-yl)cyclohexane-carboxamide with substituted aldehyde. Mass, FT-IR, NMR, and spectral techniques confirmed the synthesized ligand. The resulting compound was tested with the coordination behavior of a series of various d-block metal ions named Cu2+, Zn2+, Co2+, and Ni2+, with the prepared (BSB) reported. The bonding behavior and the complexes' performance have been assumed as p

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6

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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7

Ahmed, Amena Alyas, Natiq Ghanim Ahmed, and Ahmad Khuder Ahmad. "Synthesis of New Substituted Tetrazole and 4-Thiazolidinone from Schiff's Bases." Pakistan Journal of Scientific & Industrial Research Series A: Physical Sciences 63, no. 1 (2020): 1–11. http://dx.doi.org/10.52763/pjsir.phys.sci.63.1.2020.1.11.

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 The present work involved the synthesis of compound (1) (1-amino-4-methyl-6-phenyl pyrimidine- 2-(1H)-thione). This compound reacts with different aromatic aldehyde using glacial acetic acid as catalytic on absolute ethanol to give a new series of Schiff's bases (2-7). New thiazolidine-4-one were prepared from reactions of Schiff's bases (2,3,4,7) with thioglycolic acid in absolute ethanol giving compounds (8-11). Finally the preparation of new tetrazole derivatives (12-15) by reaction of Schiff's bases (2,3,4,7) with sodium azide in THF. The structure of the synthesized compounds are c

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8

Sahoo, C. R., R. Patro, J. Sahoo, R. N. Padhy, and S. K. Paidesetty. "DESIGN, MOLECULAR DOCKING OF SYNTHESIZED SCHIFF-BASED THIAZOLE/ PYRIDINE DERIVATIVES AS POTENT ANTIBACTERIAL INHIBITOR." INDIAN DRUGS 56, no. 11 (2019): 20–25. http://dx.doi.org/10.53879/id.56.11.12007.

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A series of N-(substituted benzylidene) thiazol-2-amines (3a-3d) and N-(substituted benzylidene) pyridyl-2-amines (3A-3D) were synthesized and individual structures were confirmed by several spectral techniques. Antibacterial activity of synthesized Schiff-base derivatives were performed by agar-diffusion method. These compounds were screened by in vitro antibacterial activity against uropathogenic bacteria, Escerichia coli and Klebsiella pneumoniae. The compounds 3a, 3B and 3d had the best inhibititory activity against K. pneumonia, whereas, the other derivatives had moderate activity. The co

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9

Singh, Gurvinder P., Saravanan Kaliyaperymal, and Gyanendra K. Sharma. "Microwave-assisted Solvent-free Synthesis of Some New 4-[2-(Substituted phenyl)-4, 5-diphenyl-1H-imidazole-1-yl]-1H-indoles of Biological Interest." INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY 34, no. 02 (2024): 253. http://dx.doi.org/10.59467/ijhc.2024.34.253.

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Solvent-free, microwave-assisted synthesis of several new indolyl imidazoles of biological importance is reported. First, indoleamine was condensed with substituted aryl aldehydes to give corresponding Schiff's bases. Then, Schiff's bases were reacted with ammonium acetate and benzil using silica gel as the solid support to yield the corresponding substituted indolyl imidazole derivatives. A comparison between the conventional approach and the microwave-assisted method is also reported in this research. All the synthesized substituted indolyl imidazole derivatives showed good antibacterial act

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10

Al-Smaism, Rafah F., Ayad M. R. Raauf, Basma M. Abd Razik, and Hala A. M. Rasheed. "Synthesis, Characterization and Antimicrobial Activityof 3-substituted Benzo[4,5]thiazolo[2,3-c][1,2,4]triazole." Al Mustansiriyah Journal of Pharmaceutical Sciences 13, no. 2 (2013): 9–15. http://dx.doi.org/10.32947/ajps.v13i2.195.

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New series of tricyclic benzo[d]thiazole derivatives (2-12) incorporated into fused to different five membered nitrogen and sulphur containing heterocyclic were prepared from 2- hydrazinobenzo[d]thiazole (1) when treated with triethylformate, acetic anhydride, ethyl chloro acetate, carbon disulphide in alkali, and urea respectively.Compound(1) converted to Schiff’s bases by the condensation different aromatic aldehydes, the synthesized Schiff’s bases were cyclized by bromine in acetic acid to form triazole ring in the new derivatives (7-11) , which might result in biologically active agents.Si

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Books on the topic "Thiazolyl substituted Schiff's bases"

1

Steele, William Leroy 1932. Infrared Study of the Carbon-Nitrogen Double Bond Absorption Frequency in Some Alkyl and Alkyl-aryl Substituted Schiff's Bases. Creative Media Partners, LLC, 2021.

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2

Steele, William Leroy 1932. Infrared Study of the Carbon-Nitrogen Double Bond Absorption Frequency in Some Alkyl and Alkyl-aryl Substituted Schiff's Bases. Creative Media Partners, LLC, 2023.

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