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Relevant bibliographies by topics / Mercaptobenzoxazole

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Journal articles

Academic literature on the topic 'Mercaptobenzoxazole'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Mercaptobenzoxazole"

1

Cheptea, Corina, Valeriu Sunel, Ana Cezarina Morosanu, et al. "Optimized Synthesis of New N-Mustards Based on 2-Mercaptobenzoxazole Derivatives with Antitumor Activity." Biomedicines 9, no. 5 (2021): 476. http://dx.doi.org/10.3390/biomedicines9050476.

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New di-(β-chloroethyl)-amides of some acids derived from 2-mercaptobenzoxazole were prepared by reaction of the corresponding pivalic mixed anhydrides with di-(β-chloroethyl)-amine. A study regarding the optimization of the chemical reactions was made for the case of di-(β-chloroethyl)-amines. The quantum chemical analysis by Spartan’14 was made in order to establish the most stable configuration of the ground electronic states for the obtained chemical structures and some physico-chemical parameters of N-mustards reported in this paper. Mercaptobenzoxazoles substituted in the side chain with

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2

Parsa, Mansoureh, Seyed Mohammad Ali Hosseini, Zahra Hassani, and Effat Jamalizadeh. "Corrosion protective properties of coatings doped with inhibitors." Anti-Corrosion Methods and Materials 61, no. 6 (2014): 416–22. http://dx.doi.org/10.1108/acmm-07-2013-1281.

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Purpose – The purpose of this paper was to study the corrosion resistance of water-based sol-gel coatings containing titania nanoparticles doped with organic inhibitors for corrosion protection of AA2024 alloy. Design/methodology/approach – The coatings were obtained using tetraethylorthosilicate, 3-glycidoxypropyltrimethoxysilane, titanium (IV) tetrapropoxide and poly(ethylene imine) polymer as cross-linking agents. As corrosions inhibitors, 2-mercaptobenzoxazole and salicylaldoxime were incorporated into the sol-gel for the improvement of the corrosion resistance. The corrosion protection pe

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3

Bozdag, Murat, Claudiu T. Supuran, Davide Esposito, et al. "2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active site." Chemical Communications 56, no. 59 (2020): 8297–300. http://dx.doi.org/10.1039/d0cc02857f.

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4

Safarova, L. R. "BIOCIDAL ACTIVITY OF AMINOMETHYL DERIVATIVES OF 2-MERCAPTOBENZOXAZOLE." Chemical Problems 20, no. 4 (2022): 366–73. http://dx.doi.org/10.32737/2221-8688-2022-3-366-373.

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The biocidal activity of the aminomethyl derivatives of 2-mercaptobenzoxazole synthesized by us and being of interest as potential antimicrobial additives to petroleum products and cutting fluids, was studied. The aminomethylation reaction proceeded with the participation of methylene-bis-amines. As a result, the appropriate N-substituted benzoxazolin-2-thiones were obtained. Their structure was proved by NMR 1H. Due to the poor solubility of the synthesized compounds in petroleum products, their salts with petroleum naphthenic acid were obtained for microbiological testing. The results of tes

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5

Santosh, Kumar Srivastava, Jain Ashish, and Devi Srivastava Savitri. "Synthesis and biological significance of 2-mercaptobenzoxazole derivatives." Journal of Indian Chemical Society Vol. 83, Nov 2006 (2006): 1118–23. https://doi.org/10.5281/zenodo.5832405.

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Synthetic Organic Chemistry Laboratory, Department of Chemistry, Dr. H. S. Gour University, Sagar-470 003, Madhya Pradesh, India E-mail : ayush_ ashu2005@yahoo.co.in <em>Manuscript received 20 December 2005, revised 2 August 2006, accepted 23 August 2006</em> Several 2-aryl-3-[(2-mercaptobenzoxazolo)acetamidyl]-4-oxothiazolidines 4, and 2-aryl-3-[(2- mercaptobenzoxazolo)acetamldyl]-5-arylidene-4-oxothiazolidines 5 have been synthesized by the appropriate methods and evaluated for their antibacterial activity against <em>\(Escherichia\) \(coli\), \(Shigella\) \(dysenteriae\),\(Streptococcus\) \

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6

Contini, G., V. Di Castro, S. Stranges, R. Richter, and M. Alagia. "Gas-Phase Photoemission Study of 2-Mercaptobenzoxazole." Journal of Physical Chemistry A 104, no. 43 (2000): 9675–80. http://dx.doi.org/10.1021/jp001979d.

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7

Trofimova, Olga, Ekaterina Grebneva, Yuliya Bolgova, et al. "The synthesis, characterization, and theoretical analysis of novel Si-substituted silylethyl derivatives of 2-mercaptobenzoxazole and 2-mercaptobenzothiazole." New Journal of Chemistry 45, no. 21 (2021): 9416–26. http://dx.doi.org/10.1039/d1nj00793a.

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Trifluorosilylethyl derivatives of 2-mercaptobenzoxazole and 2-mercaptobenzothiazole C<sub>6</sub>H<sub>4</sub>NYCS(CH<sub>2</sub>)<sub>2</sub>SiF<sub>3</sub> (Y = O, S) have been synthesized in order to study the intramolecular N → Si interaction in compounds with the SiCCSCN fragment.

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8

Nassiri, Mahmoud. "A novel, simple, and facile synthesis of 3-(3-benzyl-2,3-dihydrobenzo[d]thiazol-2-yl)benzo[d]oxazole-2(3H)-thione derivatives." Journal of Chemical Research 47, no. 2 (2023): 174751982311652. http://dx.doi.org/10.1177/17475198231165254.

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Novel 3-(3-benzyl-2,3-dihydrobenzo[ d]thiazol-2-yl)benzo[ d]oxazole-2(3 H)-thione derivatives are efficiently synthesized in excellent yields by reactions of benzothiazoles, benzyl bromides, and 2-mercaptobenzoxazole in acetone under catalyst-free conditions in the presence of triethylamine. The structures of the products are confirmed by nuclear magnetic resonance spectroscopy, infrared spectroscopy, electron ionization mass spectrometry, and elemental analyses.

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9

Yan, C. W., H. C. Lin, and C. N. Cao. "Investigation of inhibition of 2-mercaptobenzoxazole for copper corrosion." Electrochimica Acta 45, no. 17 (2000): 2815–21. http://dx.doi.org/10.1016/s0013-4686(00)00385-6.

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10

Gour, Pankaj, Lata Deshmukh, Tulshiram Dadmal, and Archana Ramteke. "Synthesis and Antimicrobial Activity of 1,2,3-Triazole Linked Benzo[d]oxazole-2-thiol/ oxazolo[4,5-b]pyridine-2-thiol Derivatives." Asian Journal of Organic & Medicinal Chemistry 6, no. 1 (2021): 7–12. http://dx.doi.org/10.14233/ajomc.2021.ajomc-p293.

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A new series of 1,2,3-triazole linked mercaptobenzoxazole/oxazolo- [4,5-b] pyridine-2-thiol derivatives (6a-j) were synthesized starting from 2-aminophenol/2-aminopyridin-3-ol in three steps via cyclization, alkylation followed by reaction with various aromatic azides using click chemistry approach. All the synthesized compounds were evaluated for their antimicrobial activity viz. E. coli, P. aeruginosa, S. aureus and S. pyogenus and three pathogenic fungi viz. C. albicans, A. niger and A. clavatus and promising compounds were identified.

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