Relevant bibliographies by topics / Cadogan reaction

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Cadogan reaction'

Author: Grafiati
Published: 4 June 2021
Last updated: 17 February 2022

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Journal articles on the topic "Cadogan reaction"

1

Qu, Zhonghua, Pu Wang, Xing Chen, Guo-Jun Deng, and Huawen Huang. "Visible-light-driven Cadogan reaction." Chinese Chemical Letters 32, no. 8 (2021): 2582–86. http://dx.doi.org/10.1016/j.cclet.2021.02.047.

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Singh, Neetu, Ga Hee Noh, Hyoung-Ryun Park, and Junseong Lee. "Crystal structure, Hirshfeld surface and photophysical analysis of 2-nitro-3-phenyl-9H-carbazole." Acta Crystallographica Section E Crystallographic Communications 77, no. 9 (2021): 887–90. http://dx.doi.org/10.1107/s2056989021007726.

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The title compound, C18H12N2O2, was synthesized from a dinitrobiphenylbenzene derivative using a novel modification of the Cadogan reaction. The reaction has several possible ring-closed products and the title compound was separated as the major product. The X-ray crystallographic study revealed that the carbazole compound crystallizes in the monoclinic P\overline{1} space group and possesses a single closed Cadogan ring. There are two independent molecules in the asymmetric unit. In the crystal, the molecules are linked by N—H...O hydrogen bonding.
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3

Castiñeira Reis, Marta, Marta Marín-Luna, Carlos Silva López, and Olalla Nieto Faza. "Mechanism of the Molybdenum-Mediated Cadogan Reaction." ACS Omega 3, no. 6 (2018): 7019–26. http://dx.doi.org/10.1021/acsomega.8b01278.

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Srour, Hassan, Thu-Hong Doan, Elisabeth Da Silva, Richard J. Whitby, and Bernhard Witulski. "Synthesis and molecular properties of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles for organic electronics obtained by a consecutive twofold Suzuki and twofold Cadogan reaction." Journal of Materials Chemistry C 4, no. 26 (2016): 6270–79. http://dx.doi.org/10.1039/c6tc02009g.

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A set of methoxy-substituted diindolo[3,2-b:2′,3′-h]carbazoles has been synthesized by twofold Suzuki–Miyaura, Cadogan andN-alkylation reactions starting fromN-hexyl-2,7-dibromo-3,6-dinitro carbazole.
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Gong, Peng, Leijiao Li, Jingbo Sun, Pengchong Xue та Ran Lu. "Synthesis of π-extended N-fused heteroacenes via regioselective Cadogan reaction". Tetrahedron Letters 57, № 13 (2016): 1468–72. http://dx.doi.org/10.1016/j.tetlet.2016.02.067.

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Bouchard, Jimmy, Salem Wakim, and Mario Leclerc. "Synthesis of Diindolocarbazoles by Cadogan Reaction: Route to Ladder Oligo(p-aniline)s." Journal of Organic Chemistry 69, no. 17 (2004): 5705–11. http://dx.doi.org/10.1021/jo049419o.

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Vogt, Astrid, Florian Henne, Christoph Wetzel, Elena Mena-Osteritz, and Peter Bäuerle. "Synthesis and characterization of S,N-heterotetracenes." Beilstein Journal of Organic Chemistry 16 (October 26, 2020): 2636–44. http://dx.doi.org/10.3762/bjoc.16.214.

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The synthesis and optoelectronic properties of novel S,N-heterotetracenes consisting of fused heterocyclic thiophene and pyrrole rings are presented. Tetracyclic and benzannulated derivatives with a varying number and sequence of sulfur and nitrogen heteroatoms were synthesized in multistep synthetic routes. A Buchwald–Hartwig amination of brominated precursors, thermolysis of azide precursors, and a Cadogan reaction of nitro-substituted precursors were successfully applied to eventually build-up pyrrole rings to stable and soluble fused systems. The various obtained heteroatom sequences ‘SSNS
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Irgashev, Roman A., Arseny A. Karmatsky, Pavel A. Slepukhin, Gennady L. Rusinov, and Valery N. Charushin. "A convenient approach to the design and synthesis of indolo[3,2-c]coumarins via the microwave-assisted Cadogan reaction." Tetrahedron Letters 54, no. 42 (2013): 5734–38. http://dx.doi.org/10.1016/j.tetlet.2013.08.030.

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Creencia, Evelyn Cuevas, Masahiro Kosaka, Toshikatsu Muramatsu, Masashi Kobayashi, Tomohiro Iizuka, and Takaaki Horaguchi. "Microwave-assisted Cadogan reaction for the synthesis of 2-aryl-2H-indazoles, 2-aryl-1H-benzimidazoles, 2-carbonylindoles, carbazole, and phenazine." Journal of Heterocyclic Chemistry 46, no. 6 (2009): 1309–17. http://dx.doi.org/10.1002/jhet.267.

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Irgashev, Roman A., Arseny A. Karmatsky, Pavel A. Slepukhin, Gennady L. Rusinov, and Valery N. Charushin. "ChemInform Abstract: A Convenient Approach to the Design and Synthesis of Indolo[3,2-c]coumarins via the Microwave-Assisted Cadogan Reaction." ChemInform 45, no. 6 (2014): no. http://dx.doi.org/10.1002/chin.201406141.

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Dissertations / Theses on the topic "Cadogan reaction"

1

Doan, Thu Hong. "Synthesis, self-assembly and photophysical evaluation of fluorophores derived from acenes, heteroacenes and quinazolines." Thesis, Normandie, 2018. http://www.theses.fr/2018NORMC205.

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Les semiconducteurs organiques (OSC) tels que les composés organiques photovoltaïques (OPVs), les diodes électroluminescentes organiques (OLEDs) ou encore les transistors organiques à effet de champ (OFETs) constituent un domaine de recherche très attractif en raison de leur potentiel en tant que couches actives dans les dispositifs optoélectroniques. Les composés aromatiques polycycliques ainsi que les hétéroaromatiques sont considérés comme des matériaux prometteurs pour les OSC en raison de leurs conductivités électriques potentielles, de leurs propriétés optiques ainsi que de leurs assembl
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Book chapters on the topic "Cadogan reaction"

1

Li, Jie Jack. "Cadogan–Sundberg indole synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_49.

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2

Hassner, A., and I. Namboothiri. "CADOGAN Nitroaromatics Cyclization to CURTIUS Acyl Azide Rearrangement." In Organic Syntheses Based on Name Reactions. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-08-096630-4.00078-7.

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Journal articles
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