Relevant bibliographies by topics / Benzimidazolone

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Benzimidazolone'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Benzimidazolone"

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Ahmad, Iftikhar, Shahid Hameed, Helmut Duddeck, Sigurd Lenzen, Ingo Rustenbeck, and Roshan Ahmad. "N-Arylsulfonyl-benzimidazolones as Potential Hypoglycemic Agents." Zeitschrift für Naturforschung B 57, no. 3 (2002): 349–54. http://dx.doi.org/10.1515/znb-2002-0315.

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Abstract1,3-Bis(arylsulfonyl)-benzimidazolones 1a-d were synthesized by reacting benzimidazolones with arenesulfonyl chlorides in the presence of NaOH. Mono(arylsulfonyl)-benzimidazolone derivatives 5a-c were prepared from benzimidazolone by protecting one of the Natoms with a tert-butoxycarbonyl group followed by arylsulfonylation and deprotection in acidic medium. The antidiabetic activity of three compounds 1a, 1c and 5a has been determined.
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Dombroski, Mark A., Michael A. Letavic, Kim F. McClure, et al. "Benzimidazolone p38 inhibitors." Bioorganic & Medicinal Chemistry Letters 14, no. 4 (2004): 919–23. http://dx.doi.org/10.1016/j.bmcl.2003.12.023.

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Amari, Mohamed, Mokhtar Fodili, Bellara Nedjar-Kolli, AlgÉrie Pascal Hoffmann, and Jacques PÉriÉ. "Reactivity studies on 4-aminopyrones: Access to benzimidazole and benzimidazolone derivatives." Journal of Heterocyclic Chemistry 39, no. 4 (2002): 811–16. http://dx.doi.org/10.1002/jhet.5570390429.

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Szadowski, Jerzy, and Zbigniew Niewiadomski. "Deaggregation of benzimidazolone azo dyes." Dyes and Pigments 33, no. 2 (1997): 97–105. http://dx.doi.org/10.1016/s0143-7208(96)00040-x.

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Yi, Wen Bin, Fang Luan, Jian Min Xiu, Lv Qi Jiang, and Chun Cai. "Triphosgene as a Safe and Environment-Friendly Carbonylation Reagent for the Preparation of 2-Benzimidazolone." Advanced Materials Research 955-959 (June 2014): 651–55. http://dx.doi.org/10.4028/www.scientific.net/amr.955-959.651.

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2-Benzimidazolone and their derivatives which have a wide range of biological and pharmaceutical activity are important intermediates for organic synthesis. Reported synthetic methods mostly involved unfriendly materials like phosgene, dimethyl carbonate and urea. This paper developed a novel method for the synthesis of 2-benzimidazolone by the reaction of o-phenylendiamine with triphosgene (BTC) instead of phosgene. BTC is a safer solid and easier to handle compared to phosgene. BTC can greatly reduce risks to both human health and the environment.
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Macho, Vendelín, Milan Králik, and Eva Bojsová. "Intramolecular Reductive Carbonylation of o-Nitroaniline by Carbon Monoxide to 2(3H)-Benzimidazolone." Collection of Czechoslovak Chemical Communications 62, no. 2 (1997): 325–30. http://dx.doi.org/10.1135/cccc19970325.

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o-Nitroaniline reacts with carbon monoxide under pressure in the presence of solvents (e.g. dioxane, tetrahydrofuran, N,N-dimethylformamide) and a catalytic system (sulfur or a low molecular sulfur compound - a basic medium - and optionally a vanadium(V) compound) at 370-445 K to give 2(3H)-benzimidazolone by intramolecular reductive carbonylation. Similarly to intermolecular carbonylation of nitroaromatic compounds also in the title reaction the efficiency of the sulfur component decreases in the order: COS > H2S >> CS2 > S. The promotor action of NH4VO3 and V2O5 is, however, less
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Amari, Mohamed, Mokhtar Fodili, Bellara Nedjar-Kolli, Pascal Hoffmann, and Jacques Perie. "ChemInform Abstract: Reactivity Studies on 4-Aminopyrones: Access to Benzimidazole and Benzimidazolone Derivatives." ChemInform 33, no. 52 (2010): no. http://dx.doi.org/10.1002/chin.200252119.

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Gu, Xinming, Zhipeng Wang, Honghua Wang, Guangyuan Zhou, and Yanmin Zhou. "Synthesis of thermally robust benzimidazolone-based wholly aromatic polyketones." RSC Advances 11, no. 10 (2021): 5444–50. http://dx.doi.org/10.1039/d0ra09831k.

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Szadowski, J., and Z. Niewiadomski. "Reactive dyes containing a benzimidazolone residue." Coloration Technology 115, no. 10 (1999): 374–77. http://dx.doi.org/10.1111/j.1478-4408.1999.tb00291.x.

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Szadowski, J., and Z. Niewiadomski. "Reactive dyes containing a benzimidazolone residue." Coloration Technology 115, no. 12 (1999): 374–77. http://dx.doi.org/10.1111/j.1478-4408.1999.tb00296.x.

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Dissertations / Theses on the topic "Benzimidazolone"

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Duffner, Jack Patrick. "Synthesis of Benzimidazolone Glucose Uptake Inhibitors." Ohio University Honors Tutorial College / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=ouhonors1524832705752963.

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Germain, A. L. "Some synthesis of benzimidazolone analogues of prostacyclin." Thesis, University of Greenwich, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.380715.

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El, Gaghlab Khattab [Verfasser]. "Benzimidazolone und Benzimidazolthione als neue Modulatoren epigenetischer Prozesse / Khattab El Gaghlab." Greifswald : Universitätsbibliothek Greifswald, 2013. http://d-nb.info/1035605341/34.

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Badarau, Eduard. "Conception, synthèse et évaluation biologique de nouvelles classes de ligands sérotoninergiques 5-HT7." Phd thesis, Université d'Orléans, 2009. http://tel.archives-ouvertes.fr/tel-00480279.

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Parmi tous les neurotransmetteurs identifiés à ce jour, la sérotonine (5-hydroxytryptamine, 5-HT) est impliquée dans le système le plus complexe de récepteurs. Parmi eux, les récepteurs 5-HT7 qui sont les derniers découverts (1993) semblent avoir des implications multiples tant au niveau central que périphérique. Le potentiel thérapeutique représenté par la découverte de ligands 5-HT7 sélectifs vis-à-vis d'autres RCPGs a motivé notre projet de recherche. Nos études sont orientées vers la conception de trois classes distinctes de ligands. Une première famille à été conçue sur une charpente benz
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Karim, Rehana. "Development of radical synthetic methodology using solid-phase organic synthesis." Thesis, Loughborough University, 2003. https://dspace.lboro.ac.uk/2134/34406.

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The synthesis of heterocycles using radical intermediates has become an important area of research in recent years. The aim of our research was to develop radical methodologies to construct heterocycles on solid-support. Tri-cyclic benzimidazole derivatives are desirable synthetic targets with a range of biological activity and are part of certain anti-tumour agents. Solid-supported radical reactions with substituted benzimidazoles were performed under different experimental conditions, including different solvents, three different resins (Wang, Merrifield and Rink) and different radical reage
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Ritchie, Michael W. "Benzimidazole nucleoside analogues as potential antiherpetic agents." Thesis, University of St Andrews, 1997. http://hdl.handle.net/10023/14245.

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White, Wade M. "Synthesis and photoluminescent properties of linear and starburst compounds based on benzimidazole, 2-(2'-pyridyl)benzimidazole and 2,2'-dipyridylamine." Thesis, Kingston, Ont. : [s.n.], 2007. http://hdl.handle.net/1974/495.

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Akpinar, Hava Zekiye. "Synthesis Of Benzimidazole Containing Donor Acceptor Electrochromic Polymers." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12613006/index.pdf.

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ABSTRACT SYNTHESIS OF BENZIMIDAZOLE CONTAINING DONOR ACCEPTOR ELECTROCHROMIC POLYMERS Akpinar, Hava Zekiye M. Sc., Department of Chemistry Supervisor: Prof. Dr. Levent Toppare February 2011, 60 pages Donor-acceptor-donor (DAD) type benzimidazole (BIm) and 3,4-ethylenedioxythiophene (EDOT) bearing monomers (4-(2,3-Dihydrothieno[3,4-b][1,4]dioxin-5-yl)-7-(2,3 dihydrothieno[3,4b][1,4] dioxin-7-yl)-2-benzyl-1H-benzo[d]imidazole (M1), 2,4-bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)-7-(2,3-dihydrothieno[3,4-b][1,4]dioxin-7-yl)-1H-benzo[d]imidazole (M2) and 4-(2,3-dihydrothieno[3,4-b][1
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Blakemore, Emily J. A. "Molecular genetics of benzimidazole resistance in Pseudocercosporella herpotrichoides." Thesis, University of Nottingham, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.276190.

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Ozelcaglayan, Ali Can. "Synthesis Of Electroactive Benzimidazole Derivatives And Their Electrochromic Properties." Master's thesis, METU, 2012. http://etd.lib.metu.edu.tr/upload/12615196/index.pdf.

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In order to study their electrochemical and optical properties, two donor-acceptordonor (D-A-D) type monomers<br>4&#039<br>-(tert-butyl)-4,7-bis(4-hexylthiophen-2- yl)spiro[benzo[d]imidazole-2,1&#039<br>-cyclohexane] (BIHT) and 4&#039<br>-(tert-butyl)-4,7-bis(2,3- dihydrothieno[3,4-b][1,4]dioxin-5-yl)spiro[benzo[d]imidazole-2,1&#039<br>-cyclohexane] (BIED), were electrochemically polymerized. These properties were investigated by cyclic voltammetry and UV&ndash<br>Vis-NIR Spectroscopy techniques. Effects of different donor groups<br>3-hexylthiophene and 3, 4-ethylenedioxythiophene (EDOT), on n
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Books on the topic "Benzimidazolone"

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

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

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Moftah, Housain Gadmoor. Incidence of resistance to benzimidazole fungicides in a field population of Venturia inaequalis. Brock University, Dept. of Biological Sciences, 2000.

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Samsonov, V. A., V. A. Kopti︠u︡g, I. K. Korobeĭnicheva, I. L. Anisimova, M. M. Mitasov, and M. I. Podgornai︠a︡. Spektry pogloshchenii︠a︡ benzofurazanov, benzofuroksanov, 2N-benzimidazolov, benzotriazopov i ikh proizvodnykh v IK- , UF- i vidimoĭ oblasti︠a︡kh. Novosibirskiĭ in-t organicheskoĭ khimii, 1986.

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Vestergaard, Aksel A. Benzimidazole: Preparation and Applications. Nova Science Publishers, Incorporated, 2020.

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Imidazole and Benzimidazole Synthesis. Elsevier, 1997. http://dx.doi.org/10.1016/b978-0-12-303190-7.x5012-2.

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Benzimidazole: Preparation and Applications. Nova Science Publishers, Incorporated, 2020.

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Marinescu, Maria, ed. Chemistry and Applications of Benzimidazole and its Derivatives. IntechOpen, 2019. http://dx.doi.org/10.5772/intechopen.81426.

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Eckert, J., P. Deplazes, and P. Kern. Alveolar echinococcosis (Echinococcus multilocularis). Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198570028.003.0061.

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In this chapter three forms of echinococcosis in humans are described that are caused by a larval stage (metacestode) of Echinococcus multilocularis Leuckart, 1863, Echinococcus oligarthrus (Diesing, 1863) or Echinococcus vogeli Rausch and Bernstein, 1972. E. multilocularis is the causative agent of alveolar echinococcosis (AE). In the human host the metacestode of E. multilocularis behaves like a malignant tumour, characterized by infiltrative proliferation and the potential to induce serious disease. The liver is nearly exclusively the primary site of metacestode development, but metastases
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Book chapters on the topic "Benzimidazolone"

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Quaranta, Laura. "Benzimidazole Fungicides." In Bioactive Heterocyclic Compound Classes. Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664412.ch9.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "116 C7H6N2 1H-Benzimidazole." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_247.

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Drobny, J. "Properties of poly(benzimidazole)." In Specialty Thermoplastics. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-46419-9_17.

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Smith, David M. "Dihydrobenzimidazoles, Benzimidazolones, Benzimidazolethiones, and Related Compounds." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187159.ch3.

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Holze, Rudolf. "Ionic conductivities of tributylmethyl-phosphonium benzimidazolate." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_1080.

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Holze, Rudolf. "Ionic conductivities of tetra-n-butyl-methylphosphonium benzimidazolate." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_1084.

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Fujimura, Makoto, Kenji Oeda, Hirokazu Inoue, and Toshiro Kato. "Mechanism of Action ofN-Phenylcarbamates in Benzimidazole-ResistantNeurosporaStrains." In ACS Symposium Series. American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0421.ch015.

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Danao, Kishor R., and Debarshi Kar Mahapatra. "Recent Advances of Benzimidazole Derivatives as Anti-Hypertensive Agents." In Biochemistry, Biophysics, and Molecular Chemistry. Apple Academic Press, 2020. http://dx.doi.org/10.1201/9780429284175-10.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) perchlorate complex with benzimidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_627.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) perchlorate complex with benzimidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_352.

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Conference papers on the topic "Benzimidazolone"

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Jordan, Allan, Ben Acton, Nicola Hamilton, et al. "Abstract 3715: Benzimidazolone sulphonamides - potent, selective and drug-like inhibitors of poly(ADP Ribose) Glycohydrolase (PARG)." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-3715.

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Lin, Hsiu-Li, Chih-Ren Hu, Po-Hao Su, Yu-Cheng Chou, and Che-Yu Lin. "Proton Exchange Membranes Based on Blends of Poly(Benzimidazole) and Butylsulfonated Poly(Beznimidazole) for High Temperature PEMFC." In ASME 2010 8th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2010. http://dx.doi.org/10.1115/fuelcell2010-33031.

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Phosphoric acid doped poly(benzimidazole) (PBI) is one of excellent candidates of proton exchange membranes for high temperature (150–180°C) proton exchange membrane fuel cells (PEMFCs). However, the strong inter-polymer hydrogen bonds cause low elongation and brittleness of PBI membranes. In this work, we synthesize poly(benzimidazole) (PBI) and butylsulfonated poly(benzimidazole) (PBI-BS), in which around 22 mole% of imidazole –NH groups of PBI are grafted with sulfonated butyl groups. We show the elongation, phosphoric acid doping level, and proton conductivity of PBI can be improved by ble
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Hanson, Linda E., Rebecca M. Davison, Gary D. Franck, and Lee Panella. "Analysis of benzimidazole-tolerance in Cercospora beticola." In 33rd Biennial Meeting of American Society of Sugarbeet Technologist. ASSBT, 2005. http://dx.doi.org/10.5274/assbt.2005.45.

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Wang, Xiaowei, and Qiang Wang. "Study on terahertz spectra of benzimidazole molecular." In 2011 23rd Chinese Control and Decision Conference (CCDC). IEEE, 2011. http://dx.doi.org/10.1109/ccdc.2011.5968693.

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Kharche, Ajay, Sandeep Waghulde, Nilesh Gorde, and Mohan Kale. "MICROWAVE ASSISTED SYNTHESIS OF 2-ARYL BENZIMIDAZOLE." In The 24th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08475.

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Ciorteanu, Roxana, Dumitrela Diaconu, Vasilichia Antoci, et al. "New hybrid quaternary salts with pyridine/benzimidazole skeleton." In New frontiers in natural product chemistry, scientific seminar with international participation. Institute of Chemistry, 2021. http://dx.doi.org/10.19261/nfnpc.2021.ab16.

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Dwivedi, Shikha, S. K. Joshi, V. K. Hinge, B. D. Shrivastava, J. Prasad, and K. Srivastava. "XAFS study of benzimidazole mixed ligand complexes of copper." In PROF. DINESH VARSHNEY MEMORIAL NATIONAL CONFERENCE ON PHYSICS AND CHEMISTRY OF MATERIALS: NCPCM 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5098748.

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Huang, Jau-Jiun, Yu-Hsiang Hung, Lik-Ka Yun, Man-kit Leung, Tien-Lung Chiu, and Jiun Haw Lee. "Novel benzimidazole/carbazole hybrid ambipolar molecules and application in PhOLEDs." In 2016 23rd International Workshop on Active-Matrix Flatpanel Displays and Devices (AM-FPD). IEEE, 2016. http://dx.doi.org/10.1109/am-fpd.2016.7543630.

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"Synthesis, Characterization and Biological Evaluation of Some Novel Benzimidazole Derivatives." In Nov. 27-28, 2017 South Africa. EARES, 2017. http://dx.doi.org/10.17758/eares.eap517214.

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Noor, Sadia. "Interaction of Benzimidazole Metal Derivatives with DNA and Micellar Media." In IBRAS 2021 INTERNATIONAL CONFERENCE ON BIOLOGICAL RESEARCH AND APPLIED SCIENCE. Juw, 2021. http://dx.doi.org/10.37962/ibras/2021/59-62.

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Reports on the topic "Benzimidazolone"

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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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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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