Relevant bibliographies by topics / N-substituted carbazoles

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

Academic literature on the topic 'N-substituted carbazoles'

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

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Journal articles on the topic "N-substituted carbazoles"

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Archana and Anandveer Sindhu. "Synthesis and Evaluation of Antipsychotic and Anticonvulsant Activity of Indol-5-YL and Benzoxazepin-4-YL Carbazoles." International Journal of ChemTech Research 13, no. 1 (2020): 38–47. http://dx.doi.org/10.20902/ijctr.2019.130105.

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Various1-(substituted indolylidenylchalconyl) carbazole(2a-2b), 1-[2’-(5’’- substituted indolyl)-1’ , 5’-benzoxazepinyl]-carbazoles(3a-3b) and 1-[2’-(5’’-substituted indolyl)-3’-(2’’’-substitutedphenyl amino)-methyl-1’, 5’-benzoxazepinyl]-carbazoles(4a-4n) have been synthesized according to scheme -1. These compounds were screened for antipsychotic and anticonvulsant activity as well as for acute toxicity. Compound 4dI.E. 1-[2’- (5’’-methoxy indolyl)-3’-(2’’’,3’’’- dichlorophenyl amino)-methyl-1’, 5’-benzoxazepinyl]- carbazoles showed most promising antipsyctotic and anticonvulsant activity wi
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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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B., P. Das, A. Begum N., N. Choudhury D., and Banerji J. "Synthesis of some N-substituted carbazoles and their larvicidal studies." Journal of Indian Chemical Society Vol. 82, Feb 2005 (2005): 158–60. https://doi.org/10.5281/zenodo.5824930.

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Department of Chemistry, Visva-Bharati, Santiniketan-731 235. India <em>E-mail</em>: bpdas2003@yahoo.co.uk Department of Chemistry, Calcutta University, Kolkata-700 009, India <em>Manuscript received 28 October 2003, revised 27 July 2004, accepted 2 September 2004</em> Some <em>N</em>-substituted carbazoles have been synthesized and a comparative larvicidal study has also been done on the larvae of <em>Culex quinquefasciatus</em>.&nbsp;
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Khare, Ekta, Zeeshan Fatima, O. P. Tiwari, Jeevan Patra, and Unnati Kushavah. "Novel Carbazoles as AChE Inhibitors: Synthesis, Molecular Docking and Dynamic Simulation Studies." Asian Journal of Chemistry 36, no. 6 (2024): 1417–22. http://dx.doi.org/10.14233/ajchem.2024.31559.

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Extensive exploration of N-substituted carbazole derivatives is underway as these compounds possess the therapeutic potential to address the neurological problems. The main aim of this study is to synthesize a series of N-substituted carbazole derivatives and investigate it’s in vitro and in silico ability to act as AChE inhibitors. The two-step synthesis was carried out that resulted in the development of novel carbazoles and then these were subsequently subjected to in vitro evaluation for acetylcholinesterase (AChE) inhibitory activity. Further to comprehend the binding interactions and est
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Natarajan, Palani, Priya Priya, and Deachen Chuskit. "Transition-metal-free and organic solvent-free conversion of N-substituted 2-aminobiaryls into corresponding carbazoles via intramolecular oxidative radical cyclization induced by peroxodisulfate." Green Chemistry 19, no. 24 (2017): 5854–61. http://dx.doi.org/10.1039/c7gc03130k.

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Mane, Jonathan Y., Kirk H. Michaelian, Stanislav R. Stoyanov, Brant E. Billinghurst, and Jianbao Zhao. "Computational and infrared spectroscopic investigations of N-substituted carbazoles." Physical Chemistry Chemical Physics 23, no. 14 (2021): 8426–38. http://dx.doi.org/10.1039/d0cp03879b.

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Kashima, Choji, Shigeki Hibi, Tatsuya Maruyama, and Yoshimori Omote. "The convenient and one-pot synthesis of N-substituted carbazoles." Tetrahedron Letters 27, no. 19 (1986): 2131–34. http://dx.doi.org/10.1016/s0040-4039(00)84467-6.

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Bonesi, Sergio M., and Rosa Erra-Balsells. "Electronic spectroscopy of carbazole and N- and C-substituted carbazoles in homogeneous media and in solid matrix." Journal of Luminescence 93, no. 1 (2001): 51–74. http://dx.doi.org/10.1016/s0022-2313(01)00173-9.

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Sezer, Esma, Belkis Ustamehmetoǧlu, and A. Sezai Saraç. "Chemical and electrochemical polymerisation of pyrrole in the presence of N-substituted carbazoles." Synthetic Metals 107, no. 1 (1999): 7–17. http://dx.doi.org/10.1016/s0379-6779(99)00114-9.

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Cattarin, Sandro, Giuliano Mengoli, Marco M. Musiani, and Berthold Schreck. "Synthesis and properties of film electrodes from n-substituted carbazoles in acid medium." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 246, no. 1 (1988): 87–100. http://dx.doi.org/10.1016/0022-0728(88)85053-8.

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Dissertations / Theses on the topic "N-substituted carbazoles"

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Hsueh, Ju-Chun, and 薛如君. "Preparation and Optoelectronic Properties of Electropolymerized Polymeric Films from Di(carbazol-9-yl)-substituted Triphenylamine and N-Phenylcarbazole Derivatives." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/tu49b9.

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碩士<br>國立臺北科技大學<br>化學工程研究所<br>101<br>Two carbazole end-capped monomers containing triphenylamine or N-phenylcarbazole as an interior core, namely 4,4’-di(carbazol-9-yl)- 4”-methoxytriphenylamine (TPA-2Cz) and 3,6-di(carbazol-9-yl)-N-(4-methoxy- phenyl)carbazole (PhCz-2Cz), were prepared by a well-known chemistry from readily available reagents. The electrochemistry and electropolymerization of these two monomers were investigated and compared with those of structurally similar analogues with tert-butyl groups attaching on the active sites of the end-capped carbazole units. The polymeric films
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Book chapters on the topic "N-substituted carbazoles"

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Mark, James E., Dale W. Schaefer, and Gui Lin. "Types of Polysiloxanes." In The Polysiloxanes. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780195181739.003.0005.

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The polysiloxane of greatest commercial importance and scientific interest is poly(dimethylsiloxane) (PDMS), [Si(CH3)2 –O –]x, a member of the symmetrical dialkyl polysiloxanes, with repeat unit [SiR2 –O –]x. This polymer is discussed extensively in the following chapters, particularly in chapter 5. Other members of this series are poly(diethylsiloxane) [Si(C2H5) –O–]x, and poly(di-n-propylsiloxane) [SiC3H7)2–O–]x. An example of an aryl member of the symmetrically substituted series is poly(diphenylsiloxane), with repeat unit [Si(C6H5)2–O–]x. This polymer is unusual because of its very high me
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Conference papers on the topic "N-substituted carbazoles"

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Wada, Tatsuo, Yadong Zhang, Hiromi Kimura-Suda, Tetsuya Aoyama, Su-An Choi, and Hiroyuki Sasabe. "Multifunctional Photoresponses in Carbazole Main-Chain Polymers." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.thc.2.

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Electronic and optical properties of organic charge-transfer (CT) compounds have attracted a lot of attention from both fundamental science and practical applications. Remarkable progress have been made in development of electroactive CT materials such as organic metals, conducting polymers, and organic photoconductors (OPCs). Among them, OPCs are widely used for electrophotographic applications. Besides photoconductive properties, it has been elucidated experimentally and theoretically that organic inter- and intracharge transfer compounds exhibit large nonlinear optical (NLO) responses. We h
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Chen, Lisa, Mona Arnold, Yonca Kittel, Rémi Blinder, Fedor Jelezko, and Alexander J. Kuehne. "2,7-substituted N-carbazole donors on tris (2,4,6-trichlorophenyl) methyl radicals with high quantum yield." In Organic and Hybrid Light Emitting Materials and Devices XXVI, edited by Tae-Woo Lee, Franky So, and Chihaya Adachi. SPIE, 2022. http://dx.doi.org/10.1117/12.2641779.

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