Relevant bibliographies by topics / Paal-Knorr

Contents

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

Academic literature on the topic 'Paal-Knorr'

Author: Grafiati
Published: 4 June 2021
Last updated: 18 June 2025

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Journal articles on the topic "Paal-Knorr"

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Abbat, Sheenu, Devendra Dhaked, Minhajul Arfeen, and Prasad V. Bharatam. "Mechanism of the Paal–Knorr reaction: the importance of water mediated hemialcohol pathway." RSC Advances 5, no. 107 (2015): 88353–66. http://dx.doi.org/10.1039/c5ra16246g.

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The mechanism of the Paal–Knorr reaction was explored using quantum chemical methods. Hydronium ion catalysed hemialcohol pathway has been established as the preferred mechanistic route for the Paal–Knorr formation of furan, pyrrole and thiophene.
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Wagh, Sachin B., Vladimir Maslivetc, James J. La Clair, and Alexander Kornienko. "A fluorescent target-guided Paal–Knorr reaction." RSC Advances 10, no. 61 (2020): 37035–39. http://dx.doi.org/10.1039/d0ra06962k.

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Truong Nguyen, Hai, Duy-Khiem Nguyen Chau, and Phuong Hoang Tran. "A green and efficient method for the synthesis of pyrroles using a deep eutectic solvent ([CholineCl][ZnCl2]3) under solvent-free sonication." New J. Chem. 41, no. 21 (2017): 12481–89. http://dx.doi.org/10.1039/c7nj02396k.

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Akbaşlar, Dilek, Onur Demirkol, and Sultan Giray. "Paal–Knorr Pyrrole Synthesis in Water." Synthetic Communications 44, no. 9 (2014): 1323–32. http://dx.doi.org/10.1080/00397911.2013.857691.

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Mou, Xue-Qing, Zheng-Liang Xu, Shao-Hua Wang, et al. "An Au(i)-catalyzed rearrangement/cyclization cascade toward the synthesis of 2-substituted-1,4,5,6-tetrahydrocyclopenta[b]pyrrole." Chemical Communications 51, no. 60 (2015): 12064–67. http://dx.doi.org/10.1039/c5cc03979g.

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Wang, Min-Ran, Jing-Yang He, Ji-Xiang He, Ke-Ke Liu, and Jing Yang. "A Paal–Knorr agent for chemoproteomic profiling of targets of isoketals in cells." Chemical Science 12, no. 43 (2021): 14557–63. http://dx.doi.org/10.1039/d1sc02230j.

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Alvi, Shakeel, and Rashid Ali. "An expeditious and highly efficient synthesis of substituted pyrroles using a low melting deep eutectic mixture." Organic & Biomolecular Chemistry 19, no. 44 (2021): 9732–45. http://dx.doi.org/10.1039/d1ob01618k.

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Menuel, S., E. Bertaut, E. Monflier, and F. Hapiot. "Cyclodextrin-based PNN supramolecular assemblies: a new class of pincer-type ligands for aqueous organometallic catalysis." Dalton Transactions 44, no. 30 (2015): 13504–12. http://dx.doi.org/10.1039/c5dt01825k.

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Kornienko, Alexander, and James J. La Clair. "Covalent modification of biological targets with natural products through Paal–Knorr pyrrole formation." Natural Product Reports 34, no. 9 (2017): 1051–60. http://dx.doi.org/10.1039/c7np00024c.

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Mateev, Emilio, Ali Irfan, Alexandrina Mateeva, Maya Georgieva, and Alexander Zlatkov. "Microwave-assisted organic synthesis of pyrroles (Review)." Pharmacia 71 (March 25, 2024): 1–10. http://dx.doi.org/10.3897/pharmacia.71.e119866.

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The detection of pyrrole rings in numerous organic compounds with various pharmacological activities, emphasizes its huge importance in medicinal chemistry. Thus, the synthesis of pyrroles continues to arouse interest and Paal-Knorr condensation is considered to be the main synthetic route. A significant advance has been made since the MW activation was introduced in the organic synthesis which can be confirmed with the rapid growth of the published papers on that topic. Microwave irradiation is gaining popularity since faster reaction time, higher yields, easier work-up and reduced energy inp
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Dissertations / Theses on the topic "Paal-Knorr"

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趙百勤 and Pak-kan Chiu. "Isolation of hydroxypyrrolines in the Paal-Knorr reaction; and the synthesis and properties of 3H-phrroles carrying an ester or nitrilegroup at C-3." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1988. http://hub.hku.hk/bib/B31231524.

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Chiu, Pak-kan. "Isolation of hydroxypyrrolines in the Paal-Knorr reaction; and the synthesis and properties of 3H-phrroles carrying an ester or nitrile group at C-3 /." [Hong Kong : University of Hong Kong], 1988. http://sunzi.lib.hku.hk/hkuto/record.jsp?B12428553.

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Truel, Isabelle. "Synthèses d'hétérocycles phosphoniques dans les séries de l'indole, du furane, du pyrrole et de la pyridazine." Rouen, 1998. http://www.theses.fr/1998ROUES062.

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Ce travail décrit de nouvelles voies de synthèse d'hétérocycles phosphoniques. La première partie concerne l'étude de la formation d'indoles phosphoniques via un intermédiaire benzénique, convenablement substitué en vue d'une hétérocyclisation. Deux voies de synthèse ont retenu notre attention nous permettant de préparer des 3-phosphonoindoles porteurs d'une fonction amine, alkyle, aryle ou hydroxyle. La première voie fait appel à une réaction de couplage entre l'orthoiodonitrobenzène et un phosphonate α-fonctionnel, puis une hydrogénation du groupement nitro suivie de la réaction de cyclisati
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Jolicoeur, Benoit. "Synthèse d'analogues de prodigiosine." Thèse, 2007. http://hdl.handle.net/1866/17991.

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Mbyas, Saroukou Mariame Scarlett. "Synthèse et étude de nouvelles molécules potentiellement polymérisables pour la fabrication de matériaux électroluminescents : analogues du 1,3,5 benzènetripyrrole, méthyle 3,5-bipyrrolebenzoate et 6,12-diméthyle-1,5-dipyrrolediazocane." Thèse, 2014. http://hdl.handle.net/1866/13695.

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Pyrroles are found in various natural products and in the chemical composition of certain drugs because of their interesting biological properties. Lipitor, Tolmetin and Amtolmetin are examples of drugs with 1,2,5-substituted pyrroles in their composition, in which biological activities have been certified. Moreover, pyrroles are used as precursors of semiconductor polymers, oligomers and dendrimers useful for the synthesis of electroluminescent materials used in devices, such as organic light-emitting diodes, field-effect transistors, solar and organic photovoltaic cells. We are interested in
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Book chapters on the topic "Paal-Knorr"

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Li, Jie Jack. "Paal-Knorr furan synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_219.

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Li, Jie Jack. "Paal-Knorr pyrrole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_220.

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Li, Jie Jack. "Paal–Knorr furan synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_201.

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Li, Jie Jack. "Paal–Knorr pyrrole synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_202.

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Li, Jie Jack. "Paal–Knorr-Pyrrol-Synthese." In Namensreaktionen. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-52850-7_113.

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Li, Jie Jack. "Paal-Knorr furan synthesis." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_208.

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Li, Jie Jack. "Paal-Knorr pyrrole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_209.

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Li, Jie Jack. "Paal–Knorr furan synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_188.

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Li, Jie Jack. "Paal–Knorr pyrrole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_189.

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Li, Jie Jack. "Paal–Knorr Pyrrole Synthesis." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_113.

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Conference papers on the topic "Paal-Knorr"

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Manicardi, Alex, Atiruj Theppawong, Marleen Van Troys, and Annemieke Madder. "Simple one-pot peptide cleavage and spontaneous macrocyclization through Paal- Knorr-like reactions using 2,5-dialkylfuran derivatives." In 37th European Peptide Symposium. The European Peptide Society, 2024. http://dx.doi.org/10.17952/37eps.2024.p2049.

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You might also be interested in the extended bibliographies on the topic 'Paal-Knorr' for particular source types:
Journal articles
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