Relevant bibliographies by topics / Carbazole derivatives

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

Academic literature on the topic 'Carbazole derivatives'

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

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Journal articles on the topic "Carbazole derivatives"

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Manu, Tripathi* Shweta Shukla Meera Kumari Amresh Gupta. "Recent advancement of carbazole hybrid: a privileged scaffold in new drug discovery." International Journal of Advances in Pharmacy Medicine and Bioallied Sciences 10, no. 3 (2022): 123–34. https://doi.org/10.5281/zenodo.7709108.

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Carbazole comprises an important class of heterocycles. Carbazole is a tricyclic molecule having a coal tar carbon backbone, and also it has the structural properties of numerous compounds used in electronics for the manufacturing of polymers or dyes and electroluminescent materials, owing to its luminous quality. It has been reported that diverse biological activities include anti-cytotoxicity, bacteria-related problems, neurological problems, etc. Some carbazole derivatives were created such carbazoles with N-substitution, benzocarbazoles, furocarbazoles, pyrrolo-carbazoles, imidazo-carbazol
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Sweta, Shukla, and Gupta Sujeet. "Carbazole derivatives: an attractive scaffold in anticancer lead discovery." International Journal of Advances in Pharmacy Medicine and Bioallied Sciences 10, no. 2 (2022): 88–93. https://doi.org/10.5281/zenodo.7066183.

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Cancer is one of the leading chronic diseases with a high mortality rate worldwide.  Current statistical studies on cancer estimates from the World Health Organization (WHO) in 2020, cancer is the first or second leading cause of death. Although cancer remains a devastating diagnosis, several decades of preclinical progress in cancer biology and biotechnology have recently led to the successful development of several biological agents that substantially improve survival and quality of life for some patients. For over half a century, the carbazole skeleton has been the key structural motif
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Karaaslan, Cigdem, Hande Gurer-Orhan, Sibel Suzen, et al. "Behaviour of 9-Ethyl-9H-carbazole Hydrazone Derivatives Against Oxidant Systems." Croatica chemica acta 92, no. 1 (2019): 87–94. http://dx.doi.org/10.5562/cca3481.

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Antioxidants are helpful in prevention of several diseases related with oxidative stress including neurodegenerative disorders. In recent studies, carbazoles were given proof of promising antioxidant activities. In this article, 9-ethyl-9H-carbazole hydrazone derivatives were synthesized, characterized and their in vitro antioxidant activity and possible cytotoxic effects were investigated. Furthermore, protective effect of the synthesized derivatives against amyloid β-induced damage in PC12 neuronal cells was examined by using MTT assay. The newly synthesized carbazoles were found to have rad
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Alrashdi, Saad, Federica Casolari, Kwaku Kyeremeh, and Hai Deng. "Chemo-Enzymatic Synthesis of Bioactive Carbazole Derivatives." SynBio 2, no. 1 (2024): 21–30. http://dx.doi.org/10.3390/synbio2010002.

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Carbazoles are key scaffolds of either antimicrobial/antiviral alkaloid natural products or therapeutics. As such, access to structurally diverse indole-containing carbazoles has attracted considerable attention. In this report, a pilot study is described using biotransformation to provide carbazoles that contain various acyl substituents. The biotransformation system contains the thiamine-diphosphate (ThDP)-dependent enzyme NzsH, the FabH-like 3-ketoacyl-ACP synthase NzsJ, and the aromatase/cyclase NzsI, encoded in the biosynthetic gene cluster (nzs) of the bacterial carbazole alkaloid natura
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Irgashev, Roman A., Nikita A. Kazin, Gennady L. Rusinov, and Valery N. Charushin. "Nitration of 5,11-dihydroindolo[3,2-b]carbazoles and synthetic applications of their nitro-substituted derivatives." Beilstein Journal of Organic Chemistry 13 (July 14, 2017): 1396–406. http://dx.doi.org/10.3762/bjoc.13.136.

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A new general approach to double nitration of 6,12-di(hetero)aryl-substituted and 6,12-unsubstituted 5,11-dialkyl-5,11-dihydroindolo[3,2-b]carbazoles by acetyl nitrate has been developed to obtain their 2,8-dinitro and 6,12-dinitro derivatives, respectively. A formation of mono-nitro derivatives (at C-2 or C-6) from the same indolo[3,2-b]carbazoles has also been observed in several cases. Reduction of 2-nitro and 2,8-dinitro derivatives with zinc powder and hydrochloric acid has afforded 2-amino- and 2,8-diamino-substituted indolo[3,2-b]carbazoles, while reduction of 6,12-dinitro derivatives u
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Nitin Kumar, Neetika lal, Vishal Nemaysh, and Pratibha Mehta Luthra. "Synthesis and in vitro anticancer activity of novel 1,4-dimethyl-9-H-carbazol-3-yl) methanamine derivatives against human glioma U87 MG cell line." World Journal of Advanced Research and Reviews 19, no. 1 (2023): 1099–108. http://dx.doi.org/10.30574/wjarr.2023.19.1.1446.

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Glioblastoma Multiforme (GBM) is most aggressive type of brain tumor in adults. 1,4-dimethyl carbazoles exhibits significant anticancer activities in literature. In this research article, we synthesized a series of novel 1,4-dimethyl-9-H-carbazol-3-yl)methanamine and its derivatives (13-24) and evaluated their in vitro cytotoxicity activities against human glioma U87 MG cell line using MTT assay for 24 h phase time period. All final carbazole derivatives were well confirmed by NMR and HRMS spectroscopy techniques. In series, few compound (15-17) found excellent in vitro anticancer activity (IC
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Jurczak, Janusz, Agnieszka Cholewiak, and Pawel Stepniak. "Linear Neutral Receptors for Anions: Synthesis, Structure and Applications." Synthesis 50, no. 23 (2018): 4555–68. http://dx.doi.org/10.1055/s-0037-1609943.

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A selective digest of linear anion receptors based on different aromatic skeletons is presented. Since the structures of anions vary from one to another, different strategies have been developed over recent years in order to bind anions efficiently and selectively. Rigidity, number of hydrogen bond donors, steric hindrance, and special preorganization of linear receptors are analyzed to shed light on the rational design of anion receptors.1 Introduction2 1,3- and 1,2-Benzene Derivatives3 1,3- and 5,7-Azulene Derivatives4 1,8-Naphthalene Derivatives5 1,8-Anthracene Derivatives6 2,6-Pyridine Der
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Caruso, Anna, Alexia Barbarossa, Alessia Carocci, Giovanni Salzano, Maria Stefania Sinicropi, and Carmela Saturnino. "Carbazole Derivatives as STAT Inhibitors: An Overview." Applied Sciences 11, no. 13 (2021): 6192. http://dx.doi.org/10.3390/app11136192.

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The carbazole class is made up of heterocyclically structured compounds first isolated from coal tar. Their structural motif is preponderant in different synthetic materials and naturally occurring alkaloids extracted from the taxonomically related higher plants of the genus Murraya, Glycosmis, and Clausena from the Rutaceae family. Concerning the biological activity of these compounds, many research groups have assessed their antiproliferative action of carbazoles on different types of tumoral cells, such as breast, cervical, ovarian, hepatic, oral cavity, and small-cell lung cancer, and unde
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Çiçek, Baki, Merve Çağlı, Remziye Tülek, and Ali Teke. "Synthesis and optical characterization of bipod carbazole derivatives." Heterocyclic Communications 26, no. 1 (2020): 148–56. http://dx.doi.org/10.1515/hc-2020-0111.

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AbstractIn this study, some new biscarbazole derivatives were synthesized for the purpose of being used in OLED technologies and related areas. The following compounds: {1,2-bis(2-(3,6-diphenyl-9H-carbazole-9-yl) ethoxy)ethane (C-1), bis[2-(2-(3,6- diphenyl-9H-carbazole-9-yl) ethoxy)etyl]ether (C-2), bis[2-(2-(3,6-di(naphthalene-1-yl)-9H-carbazol-9-yl)ethoxy)etyl]ether (C-3) and bis [2-(2-(3,6-di(naphthalene-2-yl)-9H-carbazol-9-yl)ethoxy) ethyl]ether (C-4) were synthesized by Suzuki-Miyaura Cross Coupling reactions. The structural properties of the synthesized compounds were characterized by F
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Wantulok, Jakub, Daniel Swoboda, Jacek E. Nycz, et al. "Direct Amination of Nitroquinoline Derivatives via Nucleophilic Displacement of Aromatic Hydrogen." Molecules 26, no. 7 (2021): 1857. http://dx.doi.org/10.3390/molecules26071857.

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The vicarious nucleophilic substitution of hydrogen (VNS) reaction in electron-deficient nitroquinolines was studied. Properties of all new products have been characterized by several techniques: MS, HRMS, FTIR, GC-MS, electronic absorption spectroscopy, and multinuclear NMR. The structures of 4-chloro-8-nitroquinoline, 8-(tert-butyl)-2-methyl-5-nitroquinoline, 9-(8-nitroquinolin-7-yl)-9H-carbazole and (Z)-7-(9H-carbazol-9-yl)-8-(hydroxyimino)quinolin-5(8H)-one were determined by single-crystal X-ray diffraction measurements. The 9-(8-nitroquinolin-7-yl)-9H-carbazole and (Z)-7-(9H-carbazol-9-y
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Dissertations / Theses on the topic "Carbazole derivatives"

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Scott, Tricia L. "Palladium-catalyzed synthesis of carbazole derivatives and formal total syntheses of several naturally occurring carbazole alkaloids." Morgantown, W. Va. : [West Virginia University Libraries], 2001. http://etd.wvu.edu/templates/showETD.cfm?recnum=2075.

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Thesis (Ph. D.)--West Virginia University, 2001.<br>Title from document title page. Document formatted into pages; contains x, 83 p. : ill. (some col.). Vita. Includes abstract. Includes bibliographical references (p. 75-78).
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Abualnaj, Matoka h. Mohammed A. "Diastereoselective synthetic approaches to functionalised tetrahydropyrrolo[3,4-a] carbazole derivatives." Thesis, University of Newcastle upon Tyne, 2016. http://hdl.handle.net/10443/3265.

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The heterocyclic carbazoles are privileged scaffolds present in many biologically active naturally occurring and synthetic compounds. Herein, we disclose our investigations into new approaches towards the diastereoselective synthesis of highly functionalised tetrahydropyrrolo[3,4-a] carbazole derivatives, and the subsequent evaluation of their biological activities. Our synthetic methodology is based on an initial intermolecular Diels-Alder (D-A) reaction between a substituted 3-vinyl-1H-indole 1, containing an electron withdrawing N-protecting group, and a range of dienophiles. This key step
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Li, Junming. "The performance characterization of carbazole/dibenzothiophene derivatives in modern OLEDs." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät, 2017. http://dx.doi.org/10.18452/17678.

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Ein vielversprechendes Design für organische lichtemittierende Dioden (OLEDs) verwendet eine Wirt-Gast-Strategie durch Dispergieren einer kleinen Menge eines hocheffizienten Emitters (der Gast) in eine passende Transportmatrix (der Wirt). Die Aufgabe des Wirts ist den Exzitonentranport zum Emitter sicherzustellen und den Zerfall von Triplet-Exzitonen zu verhindern, und damit eine hohe Bauteilperformance zu erreichen. Die vorliegende Arbeit konzentriert sich auf die Beziehung zwischen Molekülstruktur und optoelektrischer Eigenschaften von Carbazol/Dibenzothiophen-Derivaten. Die Untersuchung um
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Castellanos, Ortega Sonia. "Radical and non-radical carbazole derivatives formolecular electronics. Molecular Glasses and Liquid Crystals." Doctoral thesis, Universitat de Barcelona, 2010. http://hdl.handle.net/10803/2824.

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Molecular electronics is an emergent area of the new technologies related to the use of organic and biological materials in optoelectronic and electronic devices. Among the materials used in electronic applications, low molecular weight materials, or molecular materials, became of great interest in the last years, due to the advantages they present in front of the traditional polymeric materials, such as, easier synthesis, purification and characterization, and a better processability.<br/><br/>The objectives of this thesis were the preparation and characterization of new molecular materials b
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Rizzo, Francesco. "Computational characterization of carbazole-benzonitrile derivatives for applications in Organic Light Emitting Diodes." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2020. http://amslaurea.unibo.it/21022/.

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The technology of Organic Light-Emitting Diodes has reached such a high level of reliability that it can be used in various applications. The required light emission efficiency can be achieved by transforming the triplet excitons into singlet states through Reverse InterSystem Crossing (RISC), which is the main process of a general mechanism called thermally activated delayed fluorescence (TADF). In this thesis, we theoretically analyzed two carbazole-benzonitrile (donor-acceptor) derivatives, 2,5-di(9H-carbazol-9-yl)benzonitrile (p-2CzBN) and 2,3,4,5,6-penta(9H-carbazol-9-yl)benzonitrile (5C
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Li, Junming [Verfasser], Norbert [Gutachter] Koch, Christoph T. [Gutachter] Koch, and Liangsheng [Gutachter] Liao. "The performance characterization of carbazole/dibenzothiophene derivatives in modern OLEDs / Junming Li ; Gutachter: Norbert Koch, Christoph T. Koch, Liangsheng Liao." Berlin : Mathematisch-Naturwissenschaftliche Fakultät, 2017. http://d-nb.info/1124893687/34.

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Yen-FuChen and 陳彥甫. "Synthesis and Electro-optical Characterization of Carbazole Derivatives." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/71259799989594821067.

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碩士<br>國立成功大學<br>化學系碩博士班<br>98<br>Organic materials have been expected to be applicable for practical electro-luminescent devices because of their high fluorescence efficiency and semiconducting properties. Through molecular design of organic materials, we can get specific electro-optical properties. The goal of this research is to study the synthesis and the application of the light emitting materials based on carbazole. By improving electrochemical and thermal stability, the carbazole derivatives that we synthesized are more applicable in organic light emitting diode. The decomposed temperatu
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Wang, Jing-Min, and 王經閔. "Investigating the anti-tumor mechanism of carbazole derivatives." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/92424991684246041065.

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碩士<br>國立陽明大學<br>生物藥學研究所<br>100<br>G-quadruplex is a four-stranded DNA structure formed by G-rich sequence. Formation of G-quadruplex structure was shown to inhibit telomerase activity and affect gene expression at both transcription and translation levels. A G-quadruplex forming sequences was identified at the promoter of proto-oncogene Wnt-1. CD spectra analysis revealed that the sequence was capable of forming parallel form G-quadruplex. And NMR spectra also showed the sequence was capable of forming G-quadruplex stracture in the presence of potassium ion. The expressions of Wnt-1 upon G-qua
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Yang, Chih-Han, and 楊之涵. "Synthesis and Characterization of Tetraphenylethene and Carbazole Derivatives." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/cc3eqn.

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碩士<br>國立臺灣科技大學<br>材料科學與工程系<br>107<br>This thesis presents the synthesis and characterization of tetraphenylethene and carbazole derivatives. Tetraphenylethene and its derivatives feature aggregation-induced emission. Carbazole and its derivatives exhibit great thermal stability and hole-transporting property, while suffers from aggregation-caused quenching in solid state. Four star-shaped compounds containing tetraphenylethene as a core and phenyl carbazole as arms were synthesized through palladium-catalyzed Suzuki-Miyaura coupling reaction. The optical, electronic and electrochemical propert
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Li, Chiu-Ru, and 李丘如. "Synthesis and characterization of EDOT derivatives and carbazole copolymer." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/qu8273.

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碩士<br>國立高雄應用科技大學<br>化學工程與材料工程系博碩士班<br>102<br>Poly(3,4-propylenedioxythiophene) is one of PEDOT’s derivatives , it owns symmetrical structure that its conductivity and solubility is better than PEDOT. In this study , we synthesized ProDOT derivatives with symmetrical side chains via transetherification reaction ,which were ProDOT-Me , ProDOT-Et and ProDOT-Bu ,respectively to improve solubility. Carbazole is a blue light emitting material that owns great thermal stability and organic solvent solubility . A novel series of soluble alternating ProDOT/carbazole copolymer : PDOTMeCz , PDOTEtCz , PD
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Books on the topic "Carbazole derivatives"

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Caruso, Anna, ed. Carbazole Derivatives: Latest Advances and Prospects. MDPI, 2023. http://dx.doi.org/10.3390/books978-3-0365-7289-5.

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Book chapters on the topic "Carbazole derivatives"

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Boudreault, Pierre-Luc T., Jean-François Morin, and Mario Leclerc. "Synthesis of Poly(2,7-carbazole)s and Derivatives." In Design and Synthesis of Conjugated Polymers. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527629787.ch6.

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Jones, M. T., J. Roble, and Daniel J. Sandman. "Electron Paramagnetism in Poly(1,6-di-N-carbazolyl-2,4-hexadiyne) and Its Bromine Derivatives." In ACS Symposium Series. American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0337.ch019.

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Chang, Ta-Chau, and Cheng-Chung Chang. "Detection of G-Quadruplexes in Cells and Investigation of G-Quadruplex Structure of d(T2AG3)4 in K+ Solution by a Carbazole Derivative: BMVC." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-363-9_12.

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Tiwari, Aditi, Anjaneyulu Bendi, and Anirudh Singh Bhathiwal. "Carbazoles and their Derivatives as Anti-inflammatory agents." In Heterocyclic Anti-Inflammatory Agents: A Guide for Medicinal Chemists. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815223460124010010.

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Heterocyclic compounds refer to a defining class of organic compounds with vast biological applications. Heterocyclic compounds are of great significance to life for the reason that they are abundantly present in nature, such as in the form of antibiotics, hormones, vitamins, and many more. Among heterocyclic compounds, nitrogen-based heterocycles are of special biological use because of their boundless medicinal and biological applications. Carbazoles are one of several nitrogen-based, biologically active heterocyclic compounds with the chemical formula C12H9N. Carbazole moiety has diverse ph
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Knölker, Hans-Joachim. "Transition metal-mediated synthesis of carbazole derivatives." In Advances in Nitrogen Heterocycles Volume 1. Elsevier, 1995. http://dx.doi.org/10.1016/s1521-4478(06)80017-x.

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Quindt, Matías I., and Sergio M. Bonesi. "Photooxidation of thioethers: preparative and mechanistic investigations (2018–2022)." In Photochemistry. Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/bk9781837672301-00257.

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The photooxidation of thioethers under visible-light heterogeneous and homogeneous photocatalysis methodologies is reported dealing with preparative and mechanistic viewpoints of the photoreactions. The heterogeneous photocatalytic reactions involve the use of different metal–organic frameworks containing a wide variety of metals (Zr, Bi, Ru, VO2+, In, Ag, Sn, among others) providing outstanding photocatalytic performances. On the other hand, the homogeneous photocatalytic oxidation reactions of thioethers are based on visible-light photocatalytic and photoorganocatalytic methodologies. Photoc
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Leung, Man-kit. "Electrochemical Deposition of Carbazole and Triarylamine Derivatives and Their Polymeric Optoelectronic Applications." In Organic Structures Design. Pan Stanford, 2014. http://dx.doi.org/10.1201/b17788-10.

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Joule, J. A. "Indoles, isoindoles, their reduced derivatives and carbazoles." In Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds. Elsevier, 1991. http://dx.doi.org/10.1016/b978-044453347-0.50150-6.

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Conference papers on the topic "Carbazole derivatives"

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Chen, Li-Yin, and Yu-Hsiang Cheng. "Highly sensitive ammonia gas sensing up to ppb-region based on a carbazole-triazine derivative." In Organic and Hybrid Sensors and Bioelectronics XVII, edited by Ioannis Kymissis, Emil J. List-Kratochvil, and Sahika Inal. SPIE, 2024. http://dx.doi.org/10.1117/12.3027652.

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Lin, Jiann T., K. R. J. Thomas, Yu-Tai Tao, and Chung-Wen Ko. "Light-emitting carbazole derivatives for electroluminescent materials." In International Symposium on Optical Science and Technology, edited by Zakya H. Kafafi. SPIE, 2002. http://dx.doi.org/10.1117/12.457490.

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Tseng, Ting-Yuan, Wei-Wen Chen, I.-Te Chu, et al. "Fluorescence of carbazole derivatives for screening of human cancer." In Optical Imaging, Therapeutics, and Advanced Technology in Head and Neck Surgery and Otolaryngology 2019, edited by Brian J. F. Wong and Justus F. Ilgner. SPIE, 2019. http://dx.doi.org/10.1117/12.2509410.

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Leclerc, Mario, Pierre-Luc T. Boudreault, Reda Badrou Aich, Anne-Catherine Breton, and Ye Tao. "Copolymers Based on 2,7-Carbazole With Alkylated and Perfluoroalkylated Thiophene Derivatives." In 2009 MRS Fall Meetin. Materials Research Society, 2009. http://dx.doi.org/10.1557/proc-1270-ii09-02.

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Jegorovė, Aistė, Minh Anh Truong, Maryte Daskeviciene, Vygintas Jankauskas, Vytautas Getautis, and Atsushi Wakamiya. "Starburst Carbazole Derivatives as Efficient Hole Transporting Materials for Perovskite Solar Cells." In nanoGe Spring Meeting 2022. Fundació Scito, 2022. http://dx.doi.org/10.29363/nanoge.nsm.2022.371.

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Maurucaite, Adriana, Kaspars Leduskrasts, Edgars Suna, and Aivars Vembris. "Carbazole derivatives with pyridinium ion as emitters for light-emitting electrochemical cells." In Organic Electronics and Photonics: Fundamentals and Devices III, edited by Sebastian Reineke, Koen Vandewal, and Wouter Maes. SPIE, 2022. http://dx.doi.org/10.1117/12.2621829.

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Zhang, Yichi, Ping Wang, Liang Li, Zhimin Chen, Chunying He, and Yiqun Wu. "Preparation, one- and two-photon properties of carbazole derivatives containing nitrogen heterocyclic ring." In 2012 International Workshop on Information Data Storage and Ninth International Symposium on Optical Storage, edited by Fuxi Gan and Zhitang Song. SPIE, 2013. http://dx.doi.org/10.1117/12.2015015.

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Bogdal, Dariusz, Michal Pajda, and Romano Orru. "Microwave-Assisted Free Radical Polymerization Reactions of Metacrylate Derivatives Containing Carbazole in Side Chain." In The 9th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01636.

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Jędrychowska, Agnieszka, Karol Malecha, Joanna Cabaj, and Jadwiga Sołoducho. "Optical biosensor with poly[N-nonyl-3,6-bis(ethylenedioxythiophene)carbazole] matrix for monitoring of phenol derivatives." In 13th International Scientific Conference on Optical Sensors and Electronic Sensors, edited by Jacek Golebiowski and Roman Gozdur. SPIE, 2014. http://dx.doi.org/10.1117/12.2069987.

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Cheng, Ta-Hung, Yu-Sheng Hsiao, Yuan-Jay Chang, and Chih-Ping Chen. "Comprehensive Research of Carbazole-Phosphonic Acid Derivatives as Hole-Selective Layer in Inverted Perovskite Solar Cell." In 7th Asia-Pacific International Conference on Perovskite, Organic Photovoltaics and Optoelectronics. FUNDACIO DE LA COMUNITAT VALENCIANA SCITO, 2023. http://dx.doi.org/10.29363/nanoge.iperop.2024.004.

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