Academic literature on the topic 'Benzimidazoles'

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Journal articles on the topic "Benzimidazoles"

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Al-Warhi, Tarfah, Mohamed Said, Mahmoud El Hassab, et al. "Unexpected Synthesis, Single-Crystal X-ray Structure, Anticancer Activity, and Molecular Docking Studies of Certain 2–((Imidazole/Benzimidazol–2–yl)thio)–1–arylethanones." Crystals 10, no. 6 (2020): 446. http://dx.doi.org/10.3390/cryst10060446.

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In connection with our research program concerning development of novel effective benzimidazole-based anticancer candidates, herein we describe a new unexpected synthetic route to obtain a series of 2–((imidazole/benzimidazol2–yl)thio)1–arylethanones endowed with promising anti-breast cancer and Cyclin-dependent kinase 2 (CDK2) inhibitory activities. Contrary to expectations, products for the reaction of 2–mercaptoimidazole/benzimidazole 2a,b with β–keto esters 6a–c were unambiguously assigned as 2–((imidazol/benzimidazol2–yl)thio)1–arylethanones 10a–f based on NMR spectroscopy and single-crys
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Krishnamurthy, Naik, and Narashimaiah Shashikala. "Synthesis of ruthenium(II) carbonyl complexes with 2-monosubstituted and 1,2-disubstituted benzimidazoles." Journal of the Serbian Chemical Society 74, no. 10 (2009): 1085–96. http://dx.doi.org/10.2298/jsc0910085k.

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The reaction of the polymeric carbonyl complex [RuCl2(CO)2]x with 2-monosubstituted and 1,2-disubstituted benzimidazoles and 1,4-bis(benzimidazol- 2-yl)benzene (L9) in 2-methoxyethanol produces various coloured complexes of the formulae [Ru(CO)2Cl2(L)2]?xH2O (L = 1-(o-hydroxybenzyl)-2-(o-hydroxyphenyl)benzimidazole (L1), 1-(o-hydroxyphenyl)benzimidazole (L4), 1-(p-hydroxyphenyl)benzimidazole (L5), 1-(p-chlorobenzyl)-2-p-chlorophenyl) benzimidazole (L7), 1-[1-(dimethylamino)benzyl]-2-[1-(dimethylamino) phenyl]benzimidazole (L10), x = 0; L = 2-benzylbenzimidazole (L8), 1,4-bis(benzimidazol-2-yl)
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Padhy, Gopal Krishna, Jagadeesh Panda, Chandra Sekhar Patr, Saroj Kumar Raul, and Ajaya Kumar Behera. "SYNTHETIC APPROACHES OF BENZIMIDAZOLE DERIVATIVES: A REVIEW." RASAYAN Journal of Chemistry 16, no. 04 (2023): 2009–18. http://dx.doi.org/10.31788/rjc.2023.1648014.

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Benzimidazole is considered a privileged moiety for the development of molecules with therapeutic potential. Over the years several drugs viz: albendazole, pantoprazole, astemizole, telmisartan, thiabendazole, and benomyl have been developed by optimizing benzimidazole-based structures. Given the various pharmacological implications of benzimidazoles, it encourages to explore new synthetic protocols for benzimidazoles. The review presented here highlights exclusively the recent synthetic approaches to prepare benzimidazole derivatives. Numerous search engines like Science Direct, Semantic Scho
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Kumawat, Deepak, and Harshal Tare. "Benzimidazoles in Medicinal Chemistry: Current Trends and Future Opportunities." INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 15, no. 01 (2024): 554–61. http://dx.doi.org/10.25258/ijpqa.15.1.83.

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Because of their various pharmacological actions and structural plasticity, benzimidazoles, a class of heterocyclic molecules, have received much attention in medicinal chemistry. This review paper aims to provide a complete overview of the current developments and future possibilities of benzimidazoles as promising candidates for the creation of innovative therapeutic medicines. The introduction discusses the importance of benzimidazoles in medicinal chemistry, emphasizing their wide range of uses, which include antibacterial, anticancer, and central nervous system actions. The structural pro
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Song, Bomi, Eun Young Park, Kwang Joon Kim, and Sung Hwan Ki. "Repurposing of Benzimidazole Anthelmintic Drugs as Cancer Therapeutics." Cancers 14, no. 19 (2022): 4601. http://dx.doi.org/10.3390/cancers14194601.

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Benzimidazoles have shown significant promise for repurposing as a cancer therapy. The aims of this review are to investigate the possibilities and limitations of the anti-cancer effects of benzimidazole anthelmintics and to suggest ways to overcome these limitations. This review included studies on the anti-cancer effects of 11 benzimidazoles. Largely divided into three parts, i.e., preclinical anti-cancer effects, clinical anti-cancer effects, and pharmacokinetic properties, we examine the characteristics of each benzimidazole and attempt to elucidate its key properties. Although many studie
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Kumar, Sushil, Maneesha D. Sati, and S. C. Sati. "Synthesis And Biological Evaluation Of Benzimidazole Derivatives." IOSR Journal of Applied Chemistry 17, no. 12 (2024): 13–18. https://doi.org/10.9790/5736-1712011318.

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Benzimidazoles are a class of heterocyclic compounds in which a benzene ring is fused to the 4 and 5 positions of an imidazole ring. Benzimidazole refers to the parent compound, while benzimidazoles are a class of heterocyclic compounds having similar ring structures, but different substituents. Benzimidazole derivatives possess a wide range of bioactivities including antimicrobial, anthelmintic, antiviral, anticancer, and antihypertensive activities. Many compounds possessing a benzimidazole skeleton have been employed as drugs in the market. The application of benzimidazoles in other fields
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Hajnal, Kelemen, Mărcuțiu Petra Edina, Rausz Adrienn, and Papp Lajos-Attila. "Chemical and pharmacological characterization of anthelmintic benzimidazoles." Bulletin of Medical Sciences 94, no. 2 (2021): 88–96. http://dx.doi.org/10.2478/orvtudert-2021-0013.

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Abstract Benzimidazoles, which interfere with the complex life cycle of worms, are essential in the treatment of helminthiasis. Four benzimidazole antihelmintics have been used in human therapy: albendazole, mebendazole, thiabendazole, triclabendazole. The history, representatives, synthesis, physicochemical properties, structure-activity relationships of anthelmintic benzimidazoles are presented in the review, as well as the pharmacological properties and mechanism of action of these agents. In the last decade, benzimidazole carbamate-structured anthelmintics have also been studied for their
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Wang, Cheng Jun, De Yun Zeng, Shan Shan Gong, and Qi Sun. "An Unexpected Synthesis of 2H-Benzimidazole Derivatives." Advanced Materials Research 1023 (August 2014): 43–46. http://dx.doi.org/10.4028/www.scientific.net/amr.1023.43.

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Treatment of 1,2-phenylenediamines and 3-(N-phenyl-N-methyl) aminoacrolein with ZrCl4as catalyst in refluxing 95% ethanol afforded unexpected 2H-benzimidazole derivatives as the major products. It was determined that the formation of 2H-benzimidazoles was not from the decomposition of the 2-aminovinyl benzimidazoles.
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Bektas, Hakan, Canan Albay, Emre Menteşe, Bahar Bilgin Sokmen, Zafer Kurt, and Dilem Şen. "Synthesis, Antioxidant and Antiurease Activities of Some New 5,6- dichloro-2-(4-fluorobenzyl)-1H-benzimidazole Derivatives Containing Furan, Oxadiazole, Triazole and Thiadiazole Moieties." Letters in Drug Design & Discovery 16, no. 8 (2019): 939–47. http://dx.doi.org/10.2174/1570180815666180827124956.

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Background:Benzimidazoles and its derivatives have been attracting interest for many years because of their biological activities. Benzimidazoles containing different heterocyclic moieties have wide range of biological activities such as antimicrobial, antioxidant, anticancer, antiviral, etc.Methods:In this study, some benzimidazole derivatives containing furan, oxadiazole, triazole and thiadiazole moieties have been synthesized and then evaluated for their antioxidant and antiurease activities.Results:The results showed that all the tested benzimidazoles indicated remarkable urease inhibitory
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Nardi, Monica, Sonia Bonacci, Natividad Herrera Cano, Manuela Oliverio, and Antonio Procopio. "The Highly Efficient Synthesis of 1,2-Disubstituted Benzimidazoles Using Microwave Irradiation." Molecules 27, no. 5 (2022): 1751. http://dx.doi.org/10.3390/molecules27051751.

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The benzimidazole ring of the heterocyclic pharmacophores is one of the most widespread and studied systems in nature. The benzimidazole derivative synthesis study is a crucial point for the development of a clinically available benzimidazole-based drug. Here, we report a simple microwave assisted method for the synthesis of 1,2-disubstituted benzimidazoles. The combination of the molar ratio of N-phenyl-o-phenylenediamine:benzaldehyde (1:1) using microwave irradiation and only 1% mol of Er(OTf)3 provides an efficient and environmental mild access to a diversity of benzimidazoles under solvent
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Dissertations / Theses on the topic "Benzimidazoles"

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Azmus, Dora J. Taylor. "Synthesis of polybenzimidazoles from monomers containing flexible linkages." Thesis, Corvallis, Oregon : Oregon State University, 1992. http://handle.dtic.mil/100.2/ADA256976.

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Thesis (M.S.)--Oregon State University, 1993.<br>Description based on title screen as viewed on April 8, 2009. "Completed 13 May 1992, Commencement June 1993." Includes bibliographical references (p. 73-75). Also available in print.
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Matthews, Craig J. "Metal extractants based on benzimidazoles." Thesis, University of Newcastle Upon Tyne, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.297532.

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Robinson, A. G. "Synthesis and reactions of 2H-benzimidazoles." Thesis, University of Salford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.356186.

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Ragunathan, Ramanaranjinie. "Studies of certain benzimidazoles, phthalazines and phthalimides." Thesis, Brunel University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.292494.

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Wathey, William B. "The synthesis of benzimidazoles of medicinial interest." Thesis, Cardiff University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329643.

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The aim of this programme was to design and synthesize triazinobenzimidazoles that are analogous to the antihypertensive agents, hydralazine and dihydralazine. Retrosynthetic analysis of these analogues showed that the key intermediates in the synthesis were the novel [1,2,4]triazino[4,5-a]benzimidazol-l-ones and the related 1,4-diones. Existing routes to this tricyclic ring system were either limited in scope or needed expensive starting materials. Therefore, a new synthetic route to these compounds was developed using the readily available 2-acylbenzimidazoles as starting materials. These ac
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Burford, Donald L. W. "Some studies with benzimidazoles and related heterocycles." Thesis, Loughborough University, 1988. https://dspace.lboro.ac.uk/2134/33065.

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The thesis reports the first examples of Reissert compounds prepared from the benzimidazole ring system; the first examples of monocyclic five-membered ring Reissert compounds; and an exploration of the chemistry of these compounds. The key procedure for their formation utilizes trimethylsilyl cyanide in a single-phase non-aqueous medium. Previous attempts to synthesize five-membered ring Reissert compounds have failed because, under the conventional two-phase conditions, the reaction either does not proceed or ring opening of the heterocycle occurs. The reactions of benzimidazole with an acid
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Durand, Andrée. "Étude de la métabolisation du chlorhydrate de 2-(parochloro alpha-hydroxybenzyl) benzimidazole (HBBPC) : étude pharmacologique de molécules apparentées." Université Joseph Fourier (Grenoble), 1990. http://www.theses.fr/1990GRE18003.

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Bowles, Steven E. "Synthesis and characterization of annelated nitronyl nitroxides /." Thesis, Connect to this title online; UW restricted, 2005. http://hdl.handle.net/1773/11611.

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Van, Niekerk Xandri. "Rhenium complexes of benzazole derivatives." Thesis, Nelson Mandela Metropolitan University, 2017. http://hdl.handle.net/10948/21252.

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A series of rhenium(I) complexes with monodentate benzazole ligands containing the fac-[Re(CO)3]+ was synthesized. The rhenium(I) compound [ReCl(Hmbt)2(CO)3] was prepared from the reaction of [Re(CO)5Cl] and 2-aminobenzothiazole (Hmbt) in toluene. The ligand coordinates in a monodentate manner via the thiazole nitrogen atom. A similar reaction between [Re(CO)5Cl] and N-(1,3-benzothiazol-2-yl)-2- chloroacetamide (Hbct) resulted in the formation of [ReCl(Hbct)(CO)3(NCMe)], where only one ligand binds per rhenium in a monodentate fashion. The reaction of ligands 2-mercaptobenzimidazole (Hmbi) (di
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Girardeau, Elodie. "Développement et optimisation de nouvelles familles de molécules hétérocycliques ayant un intérêt commercial en tant que building blocks." Thesis, Aix-Marseille 3, 2011. http://www.theses.fr/2011AIX30030.

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Ce manuscrit décrit la synthèse et la conception de 3 nouvelles familles de molécules, les [alpha],[alpha]-diméthylamines, les 6-nitroaminopyridines et les benzimidazoles substitués. L’étude des [alpha],[alpha]-diméthylamines nous a amené à développer une voie de synthèse originale en utilisant les propriétés chimiques du chlorure de cérium, qui, lorsqu’il est complexé avec un organolithien permet d’alkyler deux fois une fonction nitrile. Une étude exhaustive des propriétés chimiques du cérium et du chlorure de cérium en synthèse organique a également été menée. La synthèse totale de la 6-nitr
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Books on the topic "Benzimidazoles"

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Moon, Denise. Synthesis of fluorinated imidazoles and benzimidazoles. University of Birmingham, 1987.

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Ragunathan, Ramanaranjinie. Studies of certain benzimidazoles, phthalazines and phthalimides. Brunel University, 1991.

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Grimmett, M. R. Imidazole and benzimidazole synthesis. Academic Press, 1997.

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Howells, Ian Robert. Synthetic studies on 1H-azepines benzimidazoles and quinoxalines. University of Salford, 1996.

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Clark, Carol Margaret. Syntheses and reactions of 2H-benzimidazoles and their N-oxides. University of Salford, 1987.

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Hazelton, Justine Charlotte. Reactions of 2H-Benzimidazoles and synthesis of some potential anthelmintics. Universityof Salford, 1989.

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Kuznetsov, Yury V. Ambiol as base of new effective drugs. Nova Science Publishers, 2008.

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E, McConnell Ernest, International Labour Organisation, International Program on Chemical Safety., United Nations Environment Programme, WHO Task Group on Environmental Health Criteria for Benzene., and World Health Organization, eds. Benzene: First draft. World Health Organization, 1993.

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W, Hershberger L., Arce G. T, World Health Organization, et al., eds. Carbendazim: First draft. World Health Organization, 1993.

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Lundrigan, John A. The characterization of new benzimidazole fungicides. Brock University, Dept. of Chemistry, 1997.

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Book chapters on the topic "Benzimidazoles"

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Mehlhorn, Heinz. "Benzimidazoles." In Encyclopedia of Parasitology. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-43978-4_386.

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Mehlhorn, Heinz. "Benzimidazoles." In Encyclopedia of Parasitology. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-27769-6_386-2.

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Preston, P. N. "Benzimidazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187159.ch1.

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Brown, E. G. "Imidazoles and benzimidazoles." In Ring Nitrogen and Key Biomolecules. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4906-8_2.

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Smith, David M. "Benzimidazoles N-Oxides." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187159.ch2.

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Rauf, Abdul, and Nida Nayyar Farshori. "Benzimidazoles, Benzothiazoles and Benzoxazoles." In SpringerBriefs in Molecular Science. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_10.

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Gribble, Gordon W., Sudipta Roy, and Sujata Roy. "Fluorinated Imidazoles and Benzimidazoles." In Fluorine in Heterocyclic Chemistry Volume 1. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04346-3_8.

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Preston, P. N. "Commercial Applications of Benzimidazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187166.ch5.

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Tennant, G. "Condensed Benzimidazoles of Type 5-6-5." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187159.ch4.

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Preston, P. N., and G. Tennant. "Condensed Benzimidazoles of Type 6-6-5." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187159.ch5.

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Conference papers on the topic "Benzimidazoles"

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Obot, Ime. "New Benzimidazole Derivatives as Corrosion Inhibitors for Carbon Steel in HCl Solution." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05941.

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Abstract The corrosion inhibtion behaviour of two new benzimidazole derivatives namely 2-(2-Bromophenyl)-1H-benzimidazole (BPBA) and 2-(2-Bromophenyl)-1-methyl-1H-benzimidazole (BPMA) on carbon steel in 0.5 M HCl solution was investigated using electrochemical methods such as potentiodynamic polarization sweeps (Tafel plots) and electrochemical impedance spectroscopy (EIS). Scanning electron microscopy (SEM), attenuated total reflectance Fourier transformed infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS) and contact angle techniques were carried out to established the
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Mangalagiu, Violeta, Dorina Amariucai-Mantu, Dumitrela Diaconu, and Vasilichia Antoci. "BENZIMIDAZOLE � PYRIDINE: A NEW TYPE OF HGHLY SENSITIVE CHEMOSENSOR FOR ZN2+." In SGEM International Multidisciplinary Scientific GeoConference. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024v/6.2/s23.01.

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Discovery of new chemosensors for M2+ cations represent a continuously and challenging issue for researcher because of their potential applications in nano and micro technologies. Among the other metals, zinc is the second most abundant transition metal ion in human body and plays a crucial role in many biological and environmental processes. In this work we present the design, synthesis and characterization of a Zn2+ chemosensors and its coordination complexes based on podants with benzimidazole - pyridine skeleton. The new chemosensor have in the same molecule a ?�reach heterocycles (benzimi
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Pino-Gonzalez, M. Soledad, and Inmaculada Martin-Torres. "Benzimidazoles from D-glucose derivatives." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a066.

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Živković, Aleksandra, and Joachim W. Engels. "Fluorinated benzenes and benzimidazoles as RNA analogues." In XIIIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507271.

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Pimenov, I. A. "THE USE OF MOLECULAR GENETIC METHODS TO DETECT HOMO- AND HETEROZYGOUS ALLELES OF THE β-TUBULIN GENE IN PARASITIC NEMATODES HAEMONCHUS CONTORTUS". У THEORY AND PRACTICE OF PARASITIC DISEASE CONTROL. VNIIP – FSC VIEV, 2025. https://doi.org/10.31016/978-5-6053355-1-1.2025.26.244-249.

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The article presents data on the use of molecular genetic tests to diagnose the occurrence of mutant alleles in the β-tubulin gene in parasitic nematodes Haemonchus contortus that lead to the formation of genetically determined resistance to benzimidazoles. The studies were conducted on parasitic nematodes isolated from the gastrointestinal tracts of sheep raised in the Stavropol Territory and the Republic of Ingushetia. On these sheep farms, regular deworming of the entire small cattle with benzimidazole preparations was carried out. To establish the taxonomic affiliation of the studied helmi
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Nitone, Umesh, Jayaveersinh Mahida, Seema Agrawal, and Ravi Patel. "Silica supported copper nano particles design from metal waste apply formation of various condensation reaction." In 7th GoGreen Summit 2021. Technoarete, 2021. http://dx.doi.org/10.36647/978-93-92106-02-6.9.

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In recent years organic chemist focused on green chemistry for organic synthesis transformations because the silica supported catalyst is more stable, efficient and easy to recover and reusable after reaction. The silica supported copper catalyst is design from E-Waste, It used for formation of benzimidazoles from diamines and aldehydes.it is very deep work done by various catalyst, we noted in our research in unique method develop for synthesis of benzimidazoles made by condensation diamine and aldehydes via silica supported copper nano particles under EtOH as reaction media . The reactions d
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Basavaraja, Siddesh M., Manjunatha C. Ramegowda, Umesha K. Bhadraiah, et al. "Novel Class of Benzimidazoles: Synthesis, Characterization and Pharmaceutical Evaluation." In RAiSE-2023. MDPI, 2023. http://dx.doi.org/10.3390/engproc2023059070.

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Cahyana, A. H., B. Ardiansah, and N. A. Asrianti. "Fe3O4 nanoparticles: An efficient and recyclable catalyst for benzimidazoles synthesis." In PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2017 (ISCPMS2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5064058.

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Figala, Volker, Ernst Sturm, Wolf-Rüdiger Ulrich, Kurt Klemm, and Michael Przybylski. "The application of 2-(2-pyridylmethylsulfinyl)benzimidazoles as new thiol reagents." In Future Aspect in Peptide Chemistry - Ringberg Conference. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199901159.

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Budeev, A. V., L. K. Sadieva, I. S. Kovalev, and G. V. Zyryanov. "Pyrene-derived benzimidazoles as fluorescent sensors for detection of fluoride anion." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087344.

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Reports on the topic "Benzimidazoles"

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Chung, Ivy. Benzimidazole as Novel Therapy for Hormone-Refractory Metastatic Prostate Cancer. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada545657.

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Alwagdani, Abdullah. Review Of mPGES-1 Inhibitors Based On The Benzoxazole And Its Isostere Scaffold For The Treatment Of Inflammatory Diseases. University of Tennessee Health Science Center, 2024. http://dx.doi.org/10.21007/com.lsp.2024.0021.

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The vital role of the prostanoid pathway in inflammation, pain, cancer, Alzheimer’s and many other diseases has attracted the drug discovery community to discover targets for therapeutic development. Although existing non-steroidal anti-inflammatory drugs (NSAIDs) inhibiting cyclooxygenases (COX) are widely used, the side effects of these NSAIDs limit the ling time medication. Microsomal prostaglandin E synthase-1 (mPGES-1) is an attractive target that is overexpressed during inflammations, and it could be a safe alternative to NSAIDs for treating inflammatory diseases.Since the discovery of m
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Forster, Amanda L., Guillaume H. R. Messin, Kirk D. Rice, Michael A. Riley, and Stephanie S. Watson. Study of acid generation from copolymer fibers based on 5-amino-2-(p-aminophenyl)-benzimidazole. National Institute of Standards and Technology, 2009. http://dx.doi.org/10.6028/nist.ir.7592.

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Su, Ning, Jerald S. Bradshaw, Xian X. Zhang, Paul B. Savage, and Krzystof E. Krakowiak. Syntheses of Diaza-18-Crown-6 Ligands Containing Two Units Each of 4-Hydroxyazobenzene, Benzimidazole, Uracil, Anthraquinone, or Ferrocene Groups. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada361715.

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Kalel, Rahul. Silica Immobilized Brønsted-Lewis Acidic Ionic Liquid : Heterogeneous catalyst for Condensation-Aromatization in the Synthesis of 2-(4-nitrophenyl)-1H-benzimidazole by cooperative catalysis. Peeref, 2023. http://dx.doi.org/10.54985/peeref.2303p6889123.

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