Relevant bibliographies by topics / Carbazol

Contents

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

Academic literature on the topic 'Carbazol'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Carbazol"

1

Luparello, Claudio, Ilenia Cruciata, Andreas C. Joerger, et al. "Genotoxicity and Epigenotoxicity of Carbazole-Derived Molecules on MCF-7 Breast Cancer Cells." International Journal of Molecular Sciences 22, no. 7 (2021): 3410. http://dx.doi.org/10.3390/ijms22073410.

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The carbazole compounds PK9320 (1-(9-ethyl-7-(furan-2-yl)-9H-carbazol-3-yl)-N-methylmethanamine) and PK9323 (1-(9-ethyl-7-(thiazol-4-yl)-9H-carbazol-3-yl)-N-methylmethanamine), second-generation analogues of PK083 (1-(9-ethyl-9H-carbazol-3-yl)-N-methylmethanamine), restore p53 signaling in Y220C p53-mutated cancer cells by binding to a mutation-induced surface crevice and acting as molecular chaperones. In the present paper, these three molecules have been tested for mutant p53-independent genotoxic and epigenomic effects on wild-type p53 MCF-7 breast adenocarcinoma cells, employing a combinat
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Sridharan, Makuteswaran, and Karnam J. R. Prasad. "Syntheses of Substituted Furo- and Pyrano-[2,3-a]carbazoles from 2-Cinnamoyl-1-hydroxycarbazoles." Zeitschrift für Naturforschung B 63, no. 9 (2008): 1112–16. http://dx.doi.org/10.1515/znb-2008-0916.

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Reaction of 2-cinnamoyl-1-hydroxycarbazoles 2a - d, with phenacyl bromide, mercuric acetate and H2O2/NaOH under different reaction conditions yielded 2-benzoyl-3-styryl-furo[2,3-a]carbazoles 3a-d, 2-benzylidene-furo[2,3-a]carbazol-3(10H)-ones 4a - d and 3-hydroxy-2-phenylpyrano- [2,3-a]carbazol-4(11H)-ones 5a - d, respectively.
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Prabakaran, Kumaresan, and Karnam Jayaramapillai Rajendra Prasad. "Synthesis of biogenetically possible 3-substituted pyrano-[2,3-a]carbazoles." Journal of Chemical Research 2009, no. 10 (2009): 619–22. http://dx.doi.org/10.3184/030823409x12523375431104.

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3-Substituted pyrano[2,3- a]carbazol-2(11 H)-ones have been synthesised by the reaction of 1-hydroxy-carbazole-2-carbaldehyde with malononitrile, ethyl cyanoacetate, Meldrum's acid, (carbethoxymethylene)triphenylphosphorane, ethyl benzoylacetate and phenylacetonitrile.
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Murali, Karunanidhi, Hazel A. Sparkes, Baskaran Vijaya Pandiyan, and Karnam Jayarampillai Rajendra Prasad. "Synthesis, photophysical properties and DFT analysis of highly substituted pyrido carbazole-based “push pull” chromophores." New Journal of Chemistry 41, no. 16 (2017): 8242–52. http://dx.doi.org/10.1039/c7nj00643h.

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A series of new fluorescent pyrido[2,3-a]carbazole derivatives were synthesized based on a four component reaction with 2,3,4,9-tetrahydro-1H-carbazol-1-one, malononitrile, and aryl/heteroaryl aldehydes in presence of NaOEt.
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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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Konidena, Rajendra Kumar, Kyung Hyung Lee, and Jun Yeob Lee. "Molecular design featuring carbazole-decorated 15H-diindolo[2,3-b:1′,2′,3′-lm]carbazole for improved efficiency and lifetime of thermally activated delayed fluorescence emitters." Journal of Materials Chemistry C 8, no. 7 (2020): 2491–99. http://dx.doi.org/10.1039/c9tc05855a.

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Ravikumar, Krishnan, Balasubramanian Sridhar, Jagadeesh Babu Nanubolu, Venkatasubramanian Hariharakrishnan, and Bandi Venugopal Rao. "Frovatriptan salts of aliphatic carboxylic acids." Acta Crystallographica Section C Crystal Structure Communications 69, no. 4 (2013): 428–35. http://dx.doi.org/10.1107/s0108270113005878.

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The interaction of the antimigraine pharmaceutical agent frovatriptan with acetic acid and succinic acid yields the salts (±)-6-carbamoyl-N-methyl-2,3,4,9-tetrahydro-1H-carbazol-3-aminium acetate, C14H18N3O+·C2H3O2−, (I), (R)-(+)-6-carbamoyl-N-methyl-2,3,4,9-tetrahydro-1H-carbazol-3-aminium 3-carboxypropanoate monohydrate, C14H18N3O+·C4H5O4−·H2O, (II), and bis[(R)-(+)-6-carbamoyl-N-methyl-2,3,4,9-tetrahydro-1H-carbazol-3-aminium] succinate trihydrate, 2C14H18N3O+·C4H4O42−·3H2O, (III). The methylazaniumyl substitutent is oriented differently in all three structures. Additionally, the amide grou
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Kim, Jae Eun, Jun Hee Kim, Wonbo Sim, and Jai Young Lee. "9-[3-(Carbazol-9-yl)-5-methylphenyl]carbazole." Acta Crystallographica Section E Structure Reports Online 69, no. 6 (2013): o828. http://dx.doi.org/10.1107/s1600536813011641.

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Kumar, V., J. Reisch, and A. Wickramasinghe. "Glycomaurin and Glycomaurrol, New Carbazole Alkaloids From Glycosmis mauritiana (Rutaceae) Bark." Australian Journal of Chemistry 42, no. 8 (1989): 1375. http://dx.doi.org/10.1071/ch9891375.

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The stem bark of Glycosmis mauritiana contained the acridone alkaloids noracronycine and des-N- methylacronycine, and two new carbazole alkaloids, 3,3,10-trimethyl-3,7-dihydropyrano[2,3-c] carbazole (glycomaurin) and 6-methyl-4-(3′-methylbut-2′-enyl)carbazol-3-ol (glycomaurrol), whose structures were confirmed by synthesis and by cyclization to dihydroglycomaurin respectively. Glycomaurin has a ring system which has not been previously found in nature.
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Asiri, Abdullah M., Osman I. Osman, Saad H. Al-Thaqafy та Salman A. Khan. "Optical properties and fluorescence quenching of carbazole containing (D–π–A) push–pull chromophores by silver nanoparticles: a detailed insight via an experimental and theoretical approach". RSC Advances 7, № 14 (2017): 8402–14. http://dx.doi.org/10.1039/c6ra25741k.

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(4Z)-4-[(9-Ethyl-9H-carbazol-3-yl)methylidene]-2-phenyl-1,3-oxazol-5(4H)-one (ECPO) was prepared by the one-pot multi-component reaction of 9-ethyl-9H-carbazole-3-carbaldehyde, hippuric acid, anhydrous sodium acetate and acetic anhydride under microwave irradiation.
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Dissertations / Theses on the topic "Carbazol"

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Gehring, André Philipe. "Biologisch aktive Carbazol-Derivate." Diss., lmu, 2013. http://nbn-resolving.de/urn:nbn:de:bvb:19-155544.

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Kutz, Sebastian K. "Regioselektive Synthese substituierter Carbazol-1,4-chinone." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2016. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-200963.

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Die Ziele dieser Arbeit waren die Darstellung der Naturstoffe Murrayachinon-B–E und Pyrayachinon-A–C, sowie die Synthese einiger nicht natürlicher, potentiell anti-Tuberkulose-aktiver Carbazole und Carbazolchinone. Für die Darstellung der aus der Pflanze Murraya euchrestifolia Hayata isolierten Naturstoffe wurden verschiedene synthetische Herangehensweisen untersucht: Die Transformation eines 7 Hydroxycarbazolchinons in die Zielverbindungen gelang nicht, ebenso wie die Syntheseroute über eine trioxygenierte Vorstufe. 7-Methoxy-3-methyl-1-tosyloxycarbazol (A) ließ sich jedoch in einer Ausbeut
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Gehring, André Philipe [Verfasser]. "Biologisch aktive Carbazol-Derivate / André Philipe Gehring." München : Verlag Dr. Hut, 2013. http://d-nb.info/1033041726/34.

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Clavijo, Allancán Graciela Andrea. "Síntesis de carbazol-tio- y aminoquinonas antitumorales." Tesis, Universidad de Chile, 2013. http://repositorio.uchile.cl/handle/2250/138265.

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Magíster en Química área de Especialización en Química Medicinal y Memoria para optar al Título de Químico<br>Los derivados quinónicos poseen interesantes aplicaciones en áreas de la química de materiales y medicinal. Estos compuestos pueden ser encontrados tanto en la naturaleza como obtenerse sintéticamente, su síntesis ha despertado interés, debido a la posibilidad de funcionalizarlas, con el objetivo de mejorar sus propiedades, y también obtener nuevas estructuras. En este trabajo se informa la síntesis y caracterización de una serie de amino-, tio- y carbazolquinonas estructuralment
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Asche, Christian. "Strukturoptimierung von Benzo(b)carbazol-Derivaten als Zytostatika." [S.l.] : [s.n.], 2002. http://deposit.ddb.de/cgi-bin/dokserv?idn=966453743.

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Strödke, Benjamin. "Carbazol- und ß-Carbolin-Derivate als neuartige Kinase-Inhibitoren." Diss., lmu, 2008. http://nbn-resolving.de/urn:nbn:de:bvb:19-86055.

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Strödke, Benjamin. "Carbazol- und b-Carbolin-Derivate als neuartige Kinase-Inhibitoren." München Verl. Dr. Hut, 2008. http://d-nb.info/989216705/04.

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Gehring, André Philipe [Verfasser], and Franz [Akademischer Betreuer] Bracher. "Biologisch aktive Carbazol-Derivate / André Philipe Gehring. Betreuer: Franz Bracher." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2013. http://d-nb.info/1033270881/34.

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Strödke, Benjamin. "Carbazol- und [beta]-Carbolinderivate [beta-Carbolinderivate] als neuartige Kinase-Inhibitoren." München Verl. Dr. Hut, 2008. http://d-nb.info/989216705/04.

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Marques, Paulo Wilmar Barbosa. "Propriedades fotofísicas do copolímero polifluoreno-carbazol e aplicações eletro-ópticas." Universidade Federal do Amazonas, 2009. http://tede.ufam.edu.br/handle/tede/4361.

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Submitted by Elaine Lucia (lucia.elaine@live.com) on 2015-07-10T19:01:54Z No. of bitstreams: 1 Dissertação - Paulo Wilmar Barbosa Marques.pdf: 10127561 bytes, checksum: c94d4262bdea3dc5af55c4c446428279 (MD5)<br>Approved for entry into archive by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br) on 2015-07-10T19:23:30Z (GMT) No. of bitstreams: 1 Dissertação - Paulo Wilmar Barbosa Marques.pdf: 10127561 bytes, checksum: c94d4262bdea3dc5af55c4c446428279 (MD5)<br>Approved for entry into archive by Divisão de Documentação/BC Biblioteca Central (ddbc@ufam.edu.br) on 2015-07-10T19:27:12
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Books on the topic "Carbazol"

1

Calero, Ricardo Carvalho. Carballo Calero. Correo Gallego, 1992.

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Martí, Victoriano García. Don Severo Carballo. Concello da Pobra do Caramiñal, 1991.

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Perrone, Alberto Mario. Aída Carballo : arte y locura. Emecé Editores, 1995.

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Ricardo, Carvalho Calero, ed. Carballo Calero: Política e cultura. Ediciós Do Castro, 1991.

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1954-, Blanco Carmen, ed. Conversas con Ricardo Carballo Calero. Galaxia, 1989.

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Anxo, Fernán-Vello Miguel, and Pillado Mayor F, eds. Conversas en Compostela con Carballo Calero. Sotelo Blanco Edicións, 1986.

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Cranmer, M. F. Carbaryl: A toxicological review and risk analysis. Intox Press, 1986.

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Alonso, Sebastián. Tres intendentes de Rosario: Lamas, Culaciati y Carballo. [Gómez Recio Ediciones], 2013.

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Escudero, Wilfredo Kapsoli. Francisco de Carbajal, o, El genio del mal. Gráfica Horizonte, 2000.

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Priego, Consuelo Martínez. Neurociencia y afectividad: La psicología de Juan Rof Carballo. Erasmus, 2012.

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Book chapters on the topic "Carbazol"

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Brunfeldt, K., K. Kovâcs, and F. Lauprêtre. "INVESTIGATION OF CARBAZOLCARBONYL-SUBSTITUTED POLY-ɑ-LYSINE, poly[N6(9H-carbazol-9-ylcarbonyl)-lysine]." In Porto Carras, Chalkidiki, Greece, Aug. 31–Sept. 5, 1986, edited by Dimitrios Theodoropoulos. De Gruyter, 1987. http://dx.doi.org/10.1515/9783110864243-085.

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Gooch, Jan W. "Carbazole." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1913.

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Bhattacharyya, P., and D. P. Chakraborty. "Carbazole Alkaloids." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1987. http://dx.doi.org/10.1007/978-3-7091-8906-1_4.

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Peter, Helga, and Thomas Penzel. "Carbachol." In Springer Reference Medizin. Springer Berlin Heidelberg, 2020. http://dx.doi.org/10.1007/978-3-642-54672-3_379-1.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_42.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_36.

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Chakraborty, D. P., and Shyamali Roy. "Carbazole Alkaloids III." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1991. http://dx.doi.org/10.1007/978-3-7091-9119-4_2.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_41.

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Chakraborty, D. P., and Shyamali Roy. "Carbazole Alkaloids IV." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6051-0_3.

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Li, Jie Jack. "Bucherer carbazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_44.

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Conference papers on the topic "Carbazol"

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Bivol, Valeriu V., Stephan V. Robu, Galina Dragalina, L. Bostan, A. M. Prisacari, and A. Coban. "New photoresists from carbazol-containing photopolymers." In 2000 International Conference on Application of Photonic Technology (ICAPT 2000), edited by Roger A. Lessard and George A. Lampropoulos. SPIE, 2000. http://dx.doi.org/10.1117/12.406305.

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Stadlbauer, Wolfgang, Hoai Dang, Bernd Knobloch, Nargues Habib, and Thomas Kappe. "Substitution and Ring Closure Reactions of Pyrido[3,2,1-jk]carbazol-6-ones." In The 8th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01967.

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Stadlbauer, Wolfgang, Hoai Dang, and Bernd Knobloch. "Synthesis and Reactions of 5-Hydroxy-pyrido[3,2,1-jk]carbazol-4,6-diones." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01389.

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Shiono, T., S. Tassavori, F. Aida, M. Aihara, and E. Hosokawa. "Improvement of AC breakdown stress of XLPE cable by adding N-Vinyl carbazol to conductive shielding layer." In Conference on Electrical Insulation & Dielectric Phenomena — Annual Report 1987. IEEE, 1987. http://dx.doi.org/10.1109/ceidp.1987.7736585.

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Bivol, Valeriu V., Stephan V. Robu, Andrei M. Andriesh, and Teodor Necsoiu. "Characterization of the photostructurable media from carbazol-containing copolymers and thermo-cross-linking media from vynil-containing copolymers." In ROMOPTO 2000: Sixth Conference on Optics, edited by Valentin I. Vlad. SPIE, 2001. http://dx.doi.org/10.1117/12.432802.

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Sun, Run G., Yunzhang Wang, Xiaoming Zou, et al. "Electroluminescence of carbazole-substituted polyacetylenes." In SPIE's International Symposium on Optical Science, Engineering, and Instrumentation, edited by Zakya H. Kafafi. SPIE, 1998. http://dx.doi.org/10.1117/12.332631.

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Bermudez, Veronica, Francois Kajzar, S. Niziol, et al. "Linear and nonlinear optical properties of polyvinyl carbazole and polyvinyl-carbazole-substituted thin films." In International Symposium on Optical Science and Technology. SPIE, 2000. http://dx.doi.org/10.1117/12.408503.

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Aoyama, Tetsuya, Takafumi Sassa, Nicolai Mooren, et al. "Photorefractive properties of conjugated carbazole polymers." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Klaus Meerholz. SPIE, 2003. http://dx.doi.org/10.1117/12.510805.

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Andreev, Vladimir A., Anatoly L. Ivanov, Sergey M. Kazakov, Alexander V. Kukhta, Dennis V. Murtazaliev, and Gennadii M. Sorokin. "Electron impact excitation of carbazole vapor." In SPIE Proceedings, edited by Victor F. Tarasenko. SPIE, 2004. http://dx.doi.org/10.1117/12.562980.

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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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Reports on the topic "Carbazol"

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Steele, W. V., and R. D. Chirico. Thermodynamics of the hydrodenitrogenation of carbazole. Office of Scientific and Technical Information (OSTI), 1991. http://dx.doi.org/10.2172/5089483.

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Barrett, Christopher J., Biswajit Choudhury, Almeria L. Natansohn, and Paul L. Rochon. Azo-Carbazole Polymethacrylates as Single-Component Electro-Optic Materials. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada348946.

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Steele, W. V., R. D. Chirico, S. E. Knipmeyer, and A. Nguyen. The thermodynamic properties of 2-aminobiphenyl (an intermediate in the carbazole/hydrogen reaction network). Office of Scientific and Technical Information (OSTI), 1990. http://dx.doi.org/10.2172/6307021.

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Page, Marion, Michael I. Haverty, and Charles E. Richmond. Residual activity of carbaryl protected lodgepole pine against mountain pine beetle, Dillon, Colorado, 1982 and 1983. U.S. Department of Agriculture, Forest Service, Pacific Southwest Forest and Range Experiment Station, 1985. http://dx.doi.org/10.2737/psw-rn-375.

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Haverty, Michael I., Patrick J. Shea, James T. Hoffman, John M. Wenz, and Kenneth E. Gibson. Effectiveness of Esfenvalerate, Cyfluthrin, and Carbaryl in Protecting Individual Lodgepole Pines and Ponderosa Pines from Attack by Dendroctonus spp. U.S. Department of Agriculture, Forest Service, Pacific Southwest Research Station, 1998. http://dx.doi.org/10.2737/psw-rp-237.

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