Academic literature on the topic 'Electroorganic'

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Journal articles on the topic "Electroorganic"

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Breinbauer, Rolf. "Electroorganic Reductions Syntheses." Synthesis 2006, no. 17 (September 2006): 2974. http://dx.doi.org/10.1055/s-2006-951382.

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Montenegro, I. "Modern electroorganic chemistry." Journal of Electroanalytical Chemistry 387, no. 1-2 (May 1995): 152. http://dx.doi.org/10.1016/0022-0728(95)90299-6.

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Gieshoff, Tile, Anton Kehl, Dieter Schollmeyer, Kevin D. Moeller, and Siegfried R. Waldvogel. "Electrochemical synthesis of benzoxazoles from anilides – a new approach to employ amidyl radical intermediates." Chemical Communications 53, no. 20 (2017): 2974–77. http://dx.doi.org/10.1039/c7cc00927e.

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Lateef, Shaik, Srinivasulu Reddy Krishna Mohan, and Srinivasulu Reddy Jayarama Reddy. "Electroorganic synthesis of benzathine." Tetrahedron Letters 48, no. 1 (January 2007): 77–80. http://dx.doi.org/10.1016/j.tetlet.2006.11.008.

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Nematollahi, Davood, and Esmail Tammari. "Electroorganic Synthesis of Catecholthioethers." Journal of Organic Chemistry 70, no. 19 (September 2005): 7769–72. http://dx.doi.org/10.1021/jo0508301.

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Waldvogel, S. R. "Challenges in Electroorganic Synthesis." Chemie Ingenieur Technik 86, no. 9 (August 28, 2014): 1447. http://dx.doi.org/10.1002/cite.201450707.

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Cantillo, David. "Synthesis of active pharmaceutical ingredients using electrochemical methods: keys to improve sustainability." Chemical Communications 58, no. 5 (2022): 619–28. http://dx.doi.org/10.1039/d1cc06296d.

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Momeni, Shima, and Davood Nematollahi. "Electrosynthesis of new quinone sulfonimide derivatives using a conventional batch and a new electrolyte-free flow cell." Green Chemistry 20, no. 17 (2018): 4036–42. http://dx.doi.org/10.1039/c8gc01727a.

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Shin, Samuel J., Sangmee Park, Jin-Young Lee, Jae Gyeong Lee, Jeongse Yun, Dae-Woong Hwang, and Taek Dong Chung. "Cathodic electroorganic reaction on silicon oxide dielectric electrode." Proceedings of the National Academy of Sciences 117, no. 52 (December 14, 2020): 32939–46. http://dx.doi.org/10.1073/pnas.2005122117.

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The faradaic reaction at the insulator is counterintuitive. For this reason, electroorganic reactions at the dielectric layer have been scarcely investigated despite their interesting aspects and opportunities. In particular, the cathodic reaction at a silicon oxide surface under a negative potential bias remains unexplored. In this study, we utilize defective 200-nm-thick n+-Si/SiO2 as a dielectric electrode for electrolysis in an H-type divided cell to demonstrate the cathodic electroorganic reaction of anthracene and its derivatives. Intriguingly, the oxidized products are generated at the cathode. The experiments under various conditions provide consistent evidence supporting that the electrochemically generated hydrogen species, supposedly the hydrogen atom, is responsible for this phenomenon. The electrogenerated hydrogen species at the dielectric layer suggests a synthetic strategy for organic molecules.
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TOKUDA, Masao. "Organometallic compounds in electroorganic synthesis." Journal of Synthetic Organic Chemistry, Japan 43, no. 6 (1985): 522–32. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.522.

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Dissertations / Theses on the topic "Electroorganic"

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Foley, Matthew P. "Explorations in electroorganic chemistry." [Bloomington, Ind.] : Indiana University, 2009. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3386676.

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Thesis (Ph.D.)--Indiana University, Dept. of Chemistry, 2009.
Title from PDF t.p. (viewed on Jul 20, 2010). Source: Dissertation Abstracts International, Volume: 70-12, Section: B, page: 7530. Adviser: Dennis G. Peters.
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Aziz, Tamsila Nayyar. "Electroorganic synthesis in microreactors." Thesis, University of Hull, 2009. http://hydra.hull.ac.uk/resources/hull:6701.

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At present, description of applications, using electrochemical micro reactor are rare. Such techniques are extremely desirable to pharmaceutical companies who are interested in the high throughput synthesis of combinatorial libraries for pharmaceutical evaluation. Furthermore, techniques such as electrochemical synthesis may be used to prepare chemicals, which are difficult to prepare by conventional techniques. The main aim of this research project was to identify any unique control, over electrochemical organic synthesis, that micro reactors offer, and the modification of methods to gain chemical and practical advantages. These advantages come from the close control that exists between flow, concentration and thermal properties with a diffusion limited small volume system. The project involved investigation of certain factors, such as concentration of reacting species, the current limitations, and process flexibility of electro organic synthesis, in micro reactors. To investigate these factors, a versatile reaction for organic synthesis Kolbe electrolysis is selected, without using an electrolyte, in order to benefit from the quick separation and purification of products. The anodic oxidation of carboxylic acids produces alkanes by dimerization of the radicals generated at the anode. To investigate this reaction, in a micro reactor environment, several batch cell/flow system arrangements were employed in order to achieve the optimum yields. Once a set of conditions giving optimum yield is established, the system will be applicable to the electrochemical synthesis, and to develop novel methods to optimize various reactions and prepare reactive intermediates in situ.
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Nad, Sukanya [Verfasser]. "Electroorganic reactions in polymer supported organic synthesis / Sukanya Nad." Dortmund : Universitätsbibliothek Technische Universität Dortmund, 2005. http://d-nb.info/1011533138/34.

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Watts, Kevin. "Design and fabrication of an electrochemical microreactor and its use in electroorganic synthesis." Thesis, Cardiff University, 2013. http://orca.cf.ac.uk/58306/.

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Organic electrochemistry provides a straight forward and efficient method for the generation of a wide variety of reactive intermediates. It does however; suffer from limitations such as the need for supporting electrolytes. The scale up process can also be difficult from preparative to large scale batch syntheses. Interest in the field of microreactor technology has grown over the last 10 to 20 years. This is due to increasing efforts in making organic chemistry a “greener” process, using less solvents and expensive chemical reagents. Combining these two fields of chemistry provides a platform for making organic electrochemistry more appealing to chemists and industry, although the technology is still in its infancy. As there are no commercially available microreactors for electroorganic synthesis, one has been designed and fabricated before it can be used for electroorganic syntheses in a flow environment.
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García, Cruz Leticia. "Electroorganic synthesis using a Polymer Electrolyte Membrane Electrochemical Reactor: electrooxidation of primary alcohols in alkaline medium." Doctoral thesis, Universidad de Alicante, 2016. http://hdl.handle.net/10045/61507.

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Santos, Dantas Tatiane Regina dos [Verfasser], and Uwe [Akademischer Betreuer] Schröder. "Electroorganic Synthesis for the Conversion of Fatty Acids and Levulinic Acid into Chemicals and Alternative Fuels / Tatiane Regina dos Santos Dantas ; Betreuer: Uwe Schröder." Braunschweig : Technische Universität Braunschweig, 2017. http://d-nb.info/1175817562/34.

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ZHUO, JIN-JIANG, and 卓錦江. "Indirect electroorganic synthsis using mediators as electrocatalyst." Thesis, 1988. http://ndltd.ncl.edu.tw/handle/12609303553620943644.

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ZHOU, ZU-MING, and 周祖明. "Studies on the syntheses of sydnone compounds by electroorganic method." Thesis, 1989. http://ndltd.ncl.edu.tw/handle/56597555911094585036.

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Felton, Greg Andrew Nicholas Bauld Nathan L. "Electroorganic synthesis inter- and intra-molecular anion radical cycloadditions, and electrogenerated base promoted coupling reactions /." 2005. http://repositories.lib.utexas.edu/bitstream/handle/2152/1545/feltong16722.pdf.

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Felton, Greg Andrew Nicholas. "Electroorganic synthesis: inter- and intra-molecular anion radical cycloadditions, and electrogenerated base promoted coupling reactions." Thesis, 2005. http://hdl.handle.net/2152/1545.

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Books on the topic "Electroorganic"

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Little, R. Daniel. Electroorganic Synthesis. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571.

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Shōno, T. Electroorganic synthesis. London: Academic Press, 1991.

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Shono, Tatsuya. Electroorganic synthesis. London: Academic Press, 1991.

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Kyriacou, Demetrios. Modern Electroorganic Chemistry. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78677-8.

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Modern electroorganic chemistry. Berlin: Springer-Verlag, 1994.

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Electroorganic reduction synthesis. Tokyo: Kodansha, 2006.

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Esmiel, Farhin. Electroorganic synthesis of Octylaniline. [s.l: s.n.], 1988.

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Torii, Sigeru, ed. Novel Trends in Electroorganic Synthesis. Tokyo: Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-65924-2.

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Electroorganic syntheses: Methods and applications. Tokyo (Japan): Kodansha, 1985.

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1932-, Torii Shigeru, and International Symposium on Electroorganic Synthesis (3rd : 1997 : Kurashiki-shi, Japan), eds. Novel trends in electroorganic synthesis. Tokyo: Springer-Verlag, 1998.

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Book chapters on the topic "Electroorganic"

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Tanaka, Hideo, Takao Nakahara, Hamid Dhimane, and Sigeru Torii. "Electroreductive Carbon-Carbon Bond-Making Reactions in Pb(O)/Pb(II) Redox Mediatory Systems. “Barbier Type” Allylation and Hydrocoupling of Imines in an Undivided Cell." In Electroorganic Synthesis, 241–47. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-33.

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Mattiello, Leonardo, and Liliana Rampazzo. "Electroreduction of 9,9′-Spirobifluorene in Dimethyiformamide: Preparation of Hydrogenated Products." In Electroorganic Synthesis, 111–19. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-16.

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Pinson, Jean, and Saveant Jean-Michel. "Electrochemical Induction of SRN1 Nucleophilic Substitution." In Electroorganic Synthesis, 29–44. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-5.

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Degrand, C., R. Prest, and P. L. Compagnon. "Synthesis of Aromatic Chalcogeno Derivatives by Electrochemically Induced SRN1 Substitution in MeCN. Advantages and Limits of the Electrochemical Technique." In Electroorganic Synthesis, 45–51. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-6.

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Yoshida, Jun-Ichi, Shogo Nakatani, and Sachihiko Isoe. "Electro-Initiated Oxygenation." In Electroorganic Synthesis, 161–68. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-23.

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Shono, Tatsuya. "Electroreductive Coupling of Carbonyl-Type Groups with Unsaturated Systems." In Electroorganic Synthesis, 67–74. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-10.

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Fuchigami, Toshio, and Akinori Konno. "Selective Organic Synthesis Using Electrogenerated Bases." In Electroorganic Synthesis, 387–94. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-53.

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Guillanton, Georges Le, and Maurice Lamant. "Electrochemical Reduction of Carbonyl Compounds Activated by a Nitrile Function. Application to 2-Cyanocycloalkanones. Some Examples of Carbon-Carbon Bond Cleavages." In Electroorganic Synthesis, 121–27. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-17.

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Schäfer, H. J., E. Cramer, A. Hembrock, and G. Matusczyk. "Anodic Oxidation of CH-Bonds in Cyclic Hydrocarbons." In Electroorganic Synthesis, 169–80. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-24.

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Inokuchi, Tsutomu, Masahiko Kusumoto, and Sigeru Torii. "Indirect Electroreduction of α,β-Epoxy and α,α-Dihalo Carbonyl Compounds with Diphenyl Diselenide or Ditelluride as a Recyclable Mediator." In Electroorganic Synthesis, 233–39. Boca Raton: Routledge, 2023. http://dx.doi.org/10.1201/9780203758571-32.

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Conference papers on the topic "Electroorganic"

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Dowlati, Bahram, and Mohamed Rozali Othman. "An electrochemical procedure coupled with a Schiff base method; application to electroorganic synthesis of new nitrogen-containing heterocycles." In THE 2013 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2013 Postgraduate Colloquium. AIP Publishing LLC, 2013. http://dx.doi.org/10.1063/1.4858752.

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