Relevant bibliographies by topics / Friedländer reaction

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

Academic literature on the topic 'Friedländer reaction'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Friedländer reaction"

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Hsiao, Yi, Nelo R. Rivera, Nobuyoshi Yasuda, David L. Hughes, and Paul J. Reider. "Highly Regioselective Friedländer Reaction." Organic Letters 3, no. 8 (2001): 1101–3. http://dx.doi.org/10.1021/ol006785v.

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Hsiao, Yi, Nelo R. Rivera, Nobuyoshi Yasuda, David L. Hughes, and Paul J. Reider. "Highly Regioselective Friedländer Reaction." Organic Letters 4, no. 7 (2002): 1243. http://dx.doi.org/10.1021/ol020048c.

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Bekolo, Henri, and Gilbert Kirsch. "Synthesis of substituted 4-azaisoindoles — New tacrine analogues." Canadian Journal of Chemistry 85, no. 1 (2007): 1–6. http://dx.doi.org/10.1139/v06-180.

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The regioselective Friedländer reaction of 3-amino-4-cyanopyrroles with a series of cyclic ketones has enabled the first reported synthesis of substituted 4-azaisoindoles. Structurally, this new class of compounds stands for the first reported 4-azaisoindole tacrine analogues. A reaction mechanism for the formation of the reported 4-azaisoindoles is proposed.Key words: 4-azaisoindoles, tacrine, Friedländer reaction, pyrroles, mechanism.
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Gupta, Anoop K., Dinesh De, and Parimal K. Bharadwaj. "A NbO type Cu(ii) metal–organic framework showing efficient catalytic activity in the Friedländer and Henry reactions." Dalton Transactions 46, no. 24 (2017): 7782–90. http://dx.doi.org/10.1039/c7dt01595j.

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López-Sanz, Jesús, Elena Pérez-Mayoral, Dana Procházková, Rosa M. Martín-Aranda, and Antonio J. López-Peinado. "Zeolites Promoting Quinoline Synthesis via Friedländer Reaction." Topics in Catalysis 53, no. 19-20 (2010): 1430–37. http://dx.doi.org/10.1007/s11244-010-9603-8.

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Lunchev, Andrey V., Vincent C. Hendrata, Aparna Jaggi, et al. "A Friedländer route to 5,7-diazapentacenes." Journal of Materials Chemistry C 6, no. 14 (2018): 3715–21. http://dx.doi.org/10.1039/c7tc05057g.

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Garrison, Aaron T., Yasmeen Abouelhassan, Hongfen Yang, Hussain H. Yousaf, Tho J. Nguyen, and Robert W. Huigens III. "Microwave-enhanced Friedländer synthesis for the rapid assembly of halogenated quinolines with antibacterial and biofilm eradication activities against drug resistant and tolerant bacteria." MedChemComm 8, no. 4 (2017): 720–24. http://dx.doi.org/10.1039/c6md00381h.

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Muchowski, Joseph M., and Michael L. Maddox. "Concerning the mechanism of the Friedländer quinoline synthesis." Canadian Journal of Chemistry 82, no. 3 (2004): 461–78. http://dx.doi.org/10.1139/v03-211.

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Detailed experiments regarding the mechanism of the Friedländer synthesis of quinolines from o-aminobenzaldehydes and simple aldehydes or ketones are described. Under the basic or acidic conditions commonly used in this reaction, it is concluded that the first step involves a slow intermolecular aldol condensation of the aldehyde or ketone with the o-aminobenzaldehyde. The aldol adduct 5 generated in this manner then undergoes very rapid cyclization to 4, which subsequently loses water to produce the quinoline derivative 8. Both 5 and 4 are too short lived to be detectable (TLC), even when del
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Wan, Junlin, Hongxin Liu, Yunjun Lan, et al. "Catalytic Asymmetric Synthesis of Atropisomeric Quinolines through the Friedländer Reaction." Synlett 30, no. 19 (2019): 2198–202. http://dx.doi.org/10.1055/s-0039-1690228.

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A phosphoric acid catalyzed atroposelective Friedländer reaction was developed in which acetylacetone and a variety of 2′-substituted 2-aminobenzophenones were successfully employed to give optically active biaryl quinolines in good yields and with high enantioselectivities.
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Gao, Wen-Yang, Kunyue Leng, Lindsay Cash, et al. "Investigation of prototypal MOFs consisting of polyhedral cages with accessible Lewis-acid sites for quinoline synthesis." Chemical Communications 51, no. 23 (2015): 4827–29. http://dx.doi.org/10.1039/c4cc09410g.

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Dissertations / Theses on the topic "Friedländer reaction"

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Mohammed, Shireen Rashid. "Development of new radical processes : approaches toward the synthesis of Eucophylline." Thesis, Bordeaux, 2014. http://www.theses.fr/2014BORD0264/document.

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L’objectif de ce travail a consisté en le développement de nouveaux processus multi-composant radicalaires et leur application en synthèse organique. Des carbo-alcénylation d'oléfines ont ainsi été réalisées avec de nouveaux précurseurs de radicaux, des oléfines diverses, en présence de Z-diphénylsulfonyléthylène comme accepteur terminal. Les conditions de la réaction ont été optimisées, en introduisant notamment la diphénylsulfonylhydrazine comme amorceur de radicaux sous irradiation UV, et substitut au couteux DTBHN. Des conditions sans étain ont également été étudiées avec l’objectif de rem
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Mazzanti, Stefano. "A novel atroposelective strategy for the synthesis of quinoline substrates." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2018. http://amslaurea.unibo.it/16660/.

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Among heterocyclic compounds, quinoline scaffold has become an important motif for the development of new pharmacological active compounds. Since the discovery of their antimalarial properties, a large variety of quinolines was found to have interesting physiological activities and displayed attractive applications for pharmaceutical industries. In accordance to the above-mentioned features, a number of methods were developed for their synthesis but enantioselective versions are still lacking in the literature. In the past decades, this question has become even more complex, with the emergenc
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Chao, Shang-Ta, and 趙尚達. "Syntheses of Quinolino-fused Bicyclo [2.2.2] octadienes and Sesquibicyclo [2.2.2] octadienes from Friedländer Reaction." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/78220567942955274303.

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碩士<br>東海大學<br>化學系<br>96<br>The Synthesis of quinolino-fused bicycle[2.2.2]octadiene 63, sesquibicyclo[2.2.2]octadienes 71, 72, 80, 81 and the corresponding quinoline derivatives 64, 73, 82, 83 has been achieved. The UV spectra of these quinoline derivatives reveal a slight transannular interaction between quinoline moiety and bridged carbon-carbon double bonds. Reduction of o-nitrobenzaldehyde gave o-aminobenzaldehyde (62). Friedländer condensation of the resultant 62 with 61, 55, 56 produced quinoline derivative 63, 71, 72 respectively. Catalytic hydrogenation of 63, 72 gave quinoline analogs
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Book chapters on the topic "Friedländer reaction"

1

Li, Jie Jack. "Friedländer synthesis." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_105.

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Li, Jie Jack. "Friedländer synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_113.

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Li, Jie Jack. "Friedländer quinoline synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_102.

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Li, Jie Jack. "Friedländer quinoline synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_110.

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Li, Jie Jack. "Friedländer Quinoline Synthesis." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_54.

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Phuan, P. W., and M. C. Kozlowski. "The Friedländer Reaction." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-01657.

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Larsen, R. D. "Reaction with Acetates: The Friedländer Quinolinone Synthesis." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00927.

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Ghobadi, Nazanin, Niousha Nazari, and Parisa Gholamzadeh. "The Friedländer reaction: A powerful strategy for the synthesis of heterocycles." In Advances in Heterocyclic Chemistry. Elsevier, 2020. http://dx.doi.org/10.1016/bs.aihch.2020.01.001.

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You might also be interested in the extended bibliographies on the topic 'Friedländer reaction' for particular source types:
Journal articles
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