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Relevant bibliographies by topics / Indolo[3,2-b]carbazoles

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Dissertations / Theses
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Academic literature on the topic 'Indolo[3,2-b]carbazoles'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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Journal articles on the topic "Indolo[3,2-b]carbazoles"

1

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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2

Yudina, Larisa N., and Jan Bergman. "Synthesis and alkylation of indolo[3,2-b]carbazoles." Tetrahedron 59, no. 8 (2003): 1265–75. http://dx.doi.org/10.1016/s0040-4020(03)00029-2.

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Van Snick, Sven, and Wim Dehaen. "Synthesis of novel 2,8-disubstituted indolo[3,2-b]carbazoles." Org. Biomol. Chem. 10, no. 1 (2012): 79–82. http://dx.doi.org/10.1039/c1ob06298k.

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Kadam, Vinay S., Prachi A. Bhatt, Himadri S. Karmakar, Sanjio S. Zade, and Arun L. Patel. "Benzimidazole‐Substituted Indolo[3,2‐ b ]carbazoles: Acid‐Responsive Probes." ChemistrySelect 4, no. 13 (2019): 3948–52. http://dx.doi.org/10.1002/slct.201804064.

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Bergman, Jan, Niklas Wahlström, and Birgitta Stensland. "Synthesis of 2,3′-Diindolylmethanes and Substituted Indolo[3,2-b]carbazoles." Synthesis 2004, no. 08 (2004): 1187–94. http://dx.doi.org/10.1055/s-2004-822347.

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Bintinger, Johannes, Shyuan Yang, Philipp Fruhmann, et al. "Synthesis, characterization and printing application of alkylated indolo[3,2-b]carbazoles." Synthetic Metals 228 (June 2017): 9–17. http://dx.doi.org/10.1016/j.synthmet.2017.04.003.

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Dmitriev, Artem V., Azat R. Yusupov, Roman A. Irgashev, et al. "Electron-hole mobility in 6,12-di(2-thienyl)indolo[3,2-b]carbazoles." Mendeleev Communications 26, no. 6 (2016): 516–17. http://dx.doi.org/10.1016/j.mencom.2016.11.019.

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Santoso, Mardi, Naresh Kumar, and David StClair Black. "Some acid-catalysed reactions of indol-3-yl and indol-2-yl disubstituted methanols." Collection of Czechoslovak Chemical Communications 74, no. 7-8 (2009): 1137–50. http://dx.doi.org/10.1135/cccc2009023.

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1-Substituted indol-3-yl and indol-2-yl disubstituted methanols do not undergo acid-catalysed trimerisation to yield indolocyclotriveratrylenes, unlike the related primary 1-substituted indol-3-yl- and -2-ylmethanols. The 1-substituted indol-3-ylmethanols 10 and 11 gave diindol-3-ylmethanes 12 and 13, respectively, on treatment with p-toluenesulfonic acid in dichloromethane. In contrast, the indol-2-ylmethanols 22 and 23 gave the reduced indolo[3,2-b]carbazoles 24 and 25, respectively, on treatment with boron trifluoride etherate in benzene. An X-ray crystal structure of compound 24 is describ

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CHANG, FangGao, RuiPing QIN, and YuRong JIANG. "A modified double Fischer cyclization of diarylhydrazones to prepare indolo[3,2-b]-carbazoles." Chinese Science Bulletin 57, no. 7 (2012): 510–13. http://dx.doi.org/10.1360/972011-2194.

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Bhuyan, Pulak, Mohit Deb, Swarup Mazumder, and Biswajita Baruah. "A Simple and Efficient Method for the Synthesis of Indolo[3,2-b]carbazoles." Synthesis 2010, no. 06 (2010): 929–32. http://dx.doi.org/10.1055/s-0029-1218644.

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Dissertations / Theses on the topic "Indolo[3,2-b]carbazoles"

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Landelle, Henriette. "Synthèse et étude physicochimique des pyridazino [4,5-b] carbazoles, benzofuro [3,2-f] phtalazines, pyrido [3', 4' : 4,5] furo [3,2-b] indoles, benzothiéno [2,3-g] cinnolines." Caen, 1988. http://www.theses.fr/1988CAEN4072.

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Letois, Bertrand. "Synthèse et étude physicochimique de nouveaux 5,11-diméthyl-6H-pyrido[3,2-b] carbazoles à visée antitumorale." Caen, 1991. http://www.theses.fr/1991CAEN4038.

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Blouin, Nicolas. "Conception, synthèse et caractérisation de poly(2,7-carbazole)s et poly(indolo[3,2-B]carbazole)s pour des applications en électronique organique." Thesis, Université Laval, 2008. http://www.theses.ulaval.ca/2008/25870/25870.pdf.

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Le développement récent de deux nouvelles classes de matériaux, les 2,7-carbazoles et les indolo[3,2 b]carbazoles, a ouvert la porte à de multiples applications. Nous nous sommes plus particulièrement intéressés aux polymères dérivés de ces structures pour une application dans le domaine des transistors organiques à effet de champ (TOEC) et des cellules photovoltaïques organiques (CPO). Les synthèses des premiers poly(indolo[3,2 b]carbazole)s ont permis de mieux comprendre les propriétés électroniques de cette classe de polymères. Des études électrochimiques ont permis de mieux comprendre le m

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Moinet-Hedin, Véronique. "Contribution à l'étude du mécanisme d'action de nouvelles drogues à potentiel antitumoral dans la série des 5,11-diméthyl-6H-pyrido(3,2-b)carbazoles." Caen, 1994. http://www.theses.fr/1994CAEN4049.

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Трофимова, К. Е., та K. E. Trofimova. "Синтез и свойства тонкопленочных структур на основе индолокарбазолов : магистерская диссертация". Master's thesis, б. и, 2020. http://hdl.handle.net/10995/94622.

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Спроектирована установка для нанесения органических покрытий. Установка термовакуумного нанесения и виртуальный прибор «ThermoVAC&Co» позволяют осуществлять синтез тонкопленочных покрытий, контролируя температуру нагрева испаряемого вещества до 500 °C. Выполнен синтез тонких пленок 5,11-диметил-5,11-дигидроиндоло [3.2-b]карбазола 5,11-дигексил-5,11-дигидроиндоло[3.2-b]карбазола, 5,11-бис(2-метоксиэтил)-5,11-дигидроиндоло[3,2-b]карбазола и 5,11-бис[2-(2-метоксиэтокси)этокси]-5,11-дигидроиндоло[3,2-b]карбазола для исследования оптических и электрических характеристик. С помощью конфокального мик

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Arzel, Erwan. "Delta-carbolines et benzo-delta-carbolines : nouvelle voie d'accès via la métallation isomérisante." Rouen, 1999. http://www.theses.fr/1999ROUES082.

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La thèse décrit une nouvelle voie d'accès aux delta-carbolines par association des réactions de métallation et de couplage croisé catalysé par le palladium. Cette stratégie, totalement convergente et régiosélective, nécessite la synthèse de la 3-fluoro-2-iodopyridine et de l'acide 2-pivaloylaminophénylboronique. L'étude de la métallation isomérisante en série quinoléine a permis d'étendre la méthode à la préparation de benzo--carbolines et de cryptolépines substituées. Enfin, la préparation d'alcaloïdes plus complexes isolés de la Cryptolepis sanguinolenta a été abordée avec les premières synt

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Boudreault, Pierre-Luc. "Synthèse et caractérisation de nouveaux semi-conducteurs organiques à base de carbazole et d'indolo[3,2-b]carbazole." Doctoral thesis, Université Laval, 2010. http://hdl.handle.net/20.500.11794/22285.

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Cette thèse porte sur la synthèse et la caractérisation de nouveaux semi-conducteurs organiques à base de carbazole et d'indolo[3,2-b]carbazole. La synthèse de petites molécules et de polymères a été accomplie dans le but de fabriquer des transistors organiques à effet de champ (TOECs). Plusieurs techniques de mise en oeuvre ont été utilisées pour déposer les films et obtenir les meilleures performances possibles. Tout d'abord, l'évaporation sous vide des petites molécules a permis d'obtenir des films avec un haut degré de cristallinité, qui furent analysés par diffraction des rayons-X (DRX) e

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Zolfigol, M. A., A. Khazaei, F. Karimitabar, et al. "Synthesis of Indolo[3,2-b]carbazoles via an Anomeric-Based Oxidation Process: A Combined Experimental and Computational Strategy." 2017. http://hdl.handle.net/10454/16993.

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No<br>Indolo[3,2-b]carbazole is a molecule of great biological significance, as it is formed in vivo after consumption of cruciferous vegetables. The reaction of 1H-indole and various aldehydes in the presence of a catalytic amount of N,2-dibromo-6-chloro-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazine-7-sulfonamide 1,1-dioxide as an efficient and homogeneous catalyst in acetonitrile at 50°C produces 6,12-disubstituted 5,7-dihydroindolo[2,3-b]carbazole with an in good to excellent yield. The presented technique offers a fast and robust method, by the use of inexpensive commercially available st

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9

Wu, Ruei-Ling, and 吳芮綾. "Gold-catalyzed Intramolecular Cyclization of Alkynyl Azides to Indolo [3,2-b]indole Derivatives." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/sveh44.

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碩士<br>國立中山大學<br>化學系研究所<br>107<br>We expect to use gold to catalyze reactions to obtain different cyclized structures, including indole-isoquinoline and compounds containing indolo[3,2-b]indole core. We found that benzonitrile was not a good nucleophile and it could not be cyclized to obtain the desired indole-isoquinoline compound. While indolo[3,2-b]indole is unstable under anbient conditions and decomposed fast under acidic conditions, we have no way to achieve it successfully; we focus on benzo[f]benzo[5,6]indolo[3,2 -b]indole, but the coupling product could not be obtained sucessfully duri

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10

Ye, Jyun-Ming, and 葉竣銘. "Synthesis of Indolo[3,2-b]indole Arene as A New Electron Donor for Organic Photovoltaic Applications." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/35604559875368521058.

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碩士<br>國立交通大學<br>應用化學系碩博士班<br>100<br>Indolo[3,2-b]indole, containing two fused indole units, is an promising and attractive electron-rich monomer for constructing donor-acceptor materials due to its planar, symmetric, and extended conjugated structure. It is of interest to incorporate indolo[3,2-b]indole unit into a donor-acceptor ??conjugated system via its 2,7 or 3,8 positions to investigate the electronic and steric effects. In this research, we have successfully developed a new synthetic scheme to prepare 2,7-dibromo-indolo[3,2-b]indole. Unexpectedly, in an attempt to make 3,8-diromo-indolo

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Book chapters on the topic "Indolo[3,2-b]carbazoles"

1

Ong, Beng S., Yiliang Wu, and Yuning Li. "Organic Semiconductors Based on Polythiophene and Indolo[3,2-b]carbazole." In Organic Electronics. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/3527608753.ch4.

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2

"9H-Indolo[2,3-c]pyrylium to 1H-Pyrrolo[3,2-h]quinoline." In Substance Index Cyclic Compounds VIII, Tricyclic compounds II, edited by Büchel, Falbe, Hagemann, et al. Georg Thieme Verlag, 2000. http://dx.doi.org/10.1055/b-0035-114888.

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Conference papers on the topic "Indolo[3,2-b]carbazoles"

1

Silva, Adriana, Maria Paulo, Maria Mendes, and Maria Santos. "New procedure for the synthesis of indolo[3,2-b]quinoline derivatives with DNA G-quadruplex stabilization capacity." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07469.

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