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Relevant bibliographies by topics / Sandmeyer's reaction

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Dissertations / Theses
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Academic literature on the topic 'Sandmeyer's reaction'

Author: Grafiati

Published: 24 April 2022

Last updated: 30 July 2025

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Journal articles on the topic "Sandmeyer's reaction"

1

Silva, Bárbara V., Flávio A. Violante, Angelo C. Pinto, and Leonardo S. Santos. "The mechanism of Sandmeyer's cyclization reaction by electrospray ionization mass spectrometry." Rapid Communications in Mass Spectrometry 25, no. 3 (2011): 423–28. http://dx.doi.org/10.1002/rcm.4869.

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Kölmel, Dominik K., Nicole Jung, and Stefan Bräse. "Azides – Diazonium Ions – Triazenes: Versatile Nitrogen-rich Functional Groups." Australian Journal of Chemistry 67, no. 3 (2014): 328. http://dx.doi.org/10.1071/ch13533.

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For more than 100 years, nitrogen-rich compounds such as azides, diazonium ions, and triazenes have proved to be extremely valuable. Because these functional groups can be easily introduced into various substrates, they are frequently used nowadays. More importantly, they can be converted into a great number of other functional groups. The scope of this article is thus to summarize possible synthetic routes for the formation of these functional groups as well as to highlight some of the most prominent applications of these exciting moieties in chemical biology and combinatorial chemistry. Many

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3

Liu, Qianyi, Beiqi Sun, Zheng Liu, et al. "A general electrochemical strategy for the Sandmeyer reaction." Chemical Science 9, no. 46 (2018): 8731–37. http://dx.doi.org/10.1039/c8sc03346c.

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Dai, Jian-Jun, Chi Fang, Bin Xiao, et al. "Copper-Promoted Sandmeyer Trifluoromethylation Reaction." Journal of the American Chemical Society 135, no. 23 (2013): 8436–39. http://dx.doi.org/10.1021/ja404217t.

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Matheis, C., B. Bayarmagnai, K. Jouvin, and L. J. Goossen. "Convenient synthesis of pentafluoroethyl thioethers via catalytic Sandmeyer reaction with a stable fluoroalkylthiolation reagent." Organic Chemistry Frontiers 3, no. 8 (2016): 949–52. http://dx.doi.org/10.1039/c6qo00194g.

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6

Al-Khuzaie, Mohammed G. A., Mahmood M. Fahad, and Ahmed Jalil Al-Safi. "A Review on Synthesis, Reaction and Biological Importance of Isatin Derivatives." Biomedicine and Chemical Sciences 3, no. 1 (2022): 193–206. http://dx.doi.org/10.48112/bcs.v1i3.221.

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Isatin is a heterocyclic nitrogen compound that has attracted much interest in recent years due to its diverse biological and pharmacological activities. It can be used in many medical and biological applications, such as antidiabetic, antibiotic, and anticancer agents. The isatin molecule can also be prepared from different substrates by various methods, such as the methods of Sandmeyer, Stolle, Gassman, Meanwell and Hewawasam and others. On the other hand, the isatin molecule can undergo various chemical reactions, such as oxidation, Friedel-Crafts reaction, ring expansion, aldol condensatio

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Mohammed, G. A. Al-Khuzaie, M. Fahad Mahmood, and Jalil Al-Safi Ahmed. "Synthesis, Reaction and Biological Importance of Isatin Derivatives." Biomedicine and Chemical Sciences, no. 3 (July 1, 2022): 193–206. https://doi.org/10.48112/bcs.v1i3.221.

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Isatin is a heterocyclic nitrogen compound that has attracted much interest in recent years due to its diverse biological and pharmacological activities. It can be used in many medical and biological applications, such as antidiabetic, antibiotic, and anticancer agents. The isatin molecule can also be prepared from different substrates by various methods, such as the methods of Sandmeyer, Stolle, Gassman, Meanwell and Hewawasam and others. On the other hand, the isatin molecule can undergo various chemical reactions, such as oxidation, Friedel-Crafts reaction, ring expansion, aldol condensatio

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8

Nazeer, Elham, Aswany U R, and Shaiju S Dharan. "2, 3-Dioxoindoline Derivatives: Synthesis, Reactions and Exploring Pharmacological Activities." International Journal of Research and Review 9, no. 12 (2022): 109–23. http://dx.doi.org/10.52403/ijrr.20221212.

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Heterocyclic compounds represent an important class of organic compounds having vivid biological and pharmacological properties. These heterocyclic moieties, either individually or in fused form, are continuously used by researchers for the creation of new drugs due to their extensive biological profile. Isatin (1 H - indole-2,3-dione), also known as (2,3- dioxoindoline, indole quinine and indenedione), exhibits a broad range of biological activity and is therefore regarded as a bio-active heterocyclic moiety. Isatin derivatives are synthesized by using two common methods such as Sandmeyer’s a

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Ghosh, Sujit, Kinkar Biswas, and Basudeb Basu. "Recent Advances in Microwave Promoted C-P Cross-coupling Reactions." Current Microwave Chemistry 7, no. 2 (2020): 112–22. http://dx.doi.org/10.2174/2213335607666200401144724.

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: Organophosphorous compounds are of potential importance in diverse fields. They are often used as intermediates for making functionalized phosphine ligands as well as find vast applications in the areas of industrial, agricultural and biological chemistry. The microwave-assisted synthesis of C-P bonds has become increasingly popular because of its various advantages over conventional heating in the perspectives of green chemistry. : This review article has primarily focused on the synthesis of various organophosphorous molecules via microwave promoted C-P cross-coupling reactions under metal

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Striela, Romualdas, Gintaras Urbelis, Jurgis Sūdžius, Sigitas Stončius, Rita Sadzevičienė, and Linas Labanauskas. "Synthesis of bromocyclopropylpyridines via the Sandmeyer reaction." Tetrahedron Letters 58, no. 17 (2017): 1681–83. http://dx.doi.org/10.1016/j.tetlet.2017.03.029.

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Dissertations / Theses on the topic "Sandmeyer's reaction"

1

Hammond, Roger C. "Kinetic studies directed towards the improvement of Sandmeyer reactions." Thesis, University of York, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296294.

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Book chapters on the topic "Sandmeyer's reaction"

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Li, Jie Jack. "Sandmeyer reaction." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_261.

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Li, Jie Jack. "Sandmeyer reaction." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_242.

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Li, Jie Jack. "Sandmeyer reaction." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_249.

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Li, Jie Jack. "Sandmeyer reaction." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_227.

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Li, Jie Jack. "Sandmeyer Reaction." In Name Reactions. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-50865-4_132.

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6

Spitzner, D. "Sandmeyer and Schiemann Reactions." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00331.

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Matsumoto, M. "Sandmeyer Reaction of Polychlorodibenzo[,][1,4]dioxinamines." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00036.

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Gallagher, P. T. "Replacement of a Diazonium Group by Chlorine (Sandmeyer Reaction)." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00972.

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9

Nelson, S. G. "Displacement of Diazonium Groups by Nucleophiles (The Sandmeyer Reaction)." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00998.

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Conference papers on the topic "Sandmeyer's reaction"

1

Asano, Yukako, Shigenori Togashi, and Yoshishige Endo. "Optimization of Chemical Reaction Processes in Microreactors Using Reaction Rate Analyses." In ASME-JSME-KSME 2011 Joint Fluids Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/ajk2011-36013.

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We applied microreactors to the three following reactions: a consecutive bromination reaction, the two-step Sandmeyer reaction, and an acetylation reaction including solvent effects. We obtained the reaction rate constants from few experimental data or quantum chemical calculations and optimized the reaction conditions such as the reaction times and temperature. We then experimentally validated them by microreactors. A consecutive bromination reaction, where the objective reaction was followed by the side reaction, was one of the processes. The reaction temperature played an important role in

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Quattrociocchi, Daniel Garcez Santos, Antonio Rafael de Oliveira, Douglas da Motta Pio, and Vinicius Rangel Campos. "Estudo teórico da formação da isatina e de seus derivados dimetoxilados pelo método Sandmeyer." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020109.

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Isatin has been attracted the researchers attention due the structural versatility and can be used to synthesized other molecules with pharmacological activities. The Sandmeyer method is one of the most common methods for the synthesis of this molecule. Where the reaction with from aniline with chloral hydrate and hydroxyl amine occurs with good yield. When the same reaction is performed with dimethoxylated aniline show low yield or is not observed experimentally. These observations motivate this work and the justification for these facts are given in terms of thermodynamic parameters and by t

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