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Journal articles on the topic 'Electroorganic'

Author: Grafiati
Published: 7 September 2023

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

BECK, Fritz, and Hiroshi SUGINOME. "Industrial Electroorganic Synthesis in Europe." Journal of Synthetic Organic Chemistry, Japan 49, no. 9 (1991): 798–808. http://dx.doi.org/10.5059/yukigoseikyokaishi.49.798.

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12

TORII, Sigeru. "Organometal Complexes in Electroorganic Synthesis." Journal of Synthetic Organic Chemistry, Japan 51, no. 11 (1993): 1024–42. http://dx.doi.org/10.5059/yukigoseikyokaishi.51.1024.

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13

Yoshida, Jun-ichi, Kazuhide Kataoka, Roberto Horcajada, and Aiichiro Nagaki. "Modern Strategies in Electroorganic Synthesis." Chemical Reviews 108, no. 7 (July 2008): 2265–99. http://dx.doi.org/10.1021/cr0680843.

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14

Elsherbini, Mohamed, and Thomas Wirth. "Electroorganic Synthesis under Flow Conditions." Accounts of Chemical Research 52, no. 12 (November 6, 2019): 3287–96. http://dx.doi.org/10.1021/acs.accounts.9b00497.

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15

Gütz, Christoph, Bernhard Klöckner, and Siegfried R. Waldvogel. "Electrochemical Screening for Electroorganic Synthesis." Organic Process Research & Development 20, no. 1 (December 21, 2015): 26–32. http://dx.doi.org/10.1021/acs.oprd.5b00377.

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16

Atobe, Mahito, Yoshifumi Kado, and Tsutomu Nonaka. "Ultrasonic effects on electroorganic processes." Ultrasonics Sonochemistry 7, no. 3 (July 2000): 97–102. http://dx.doi.org/10.1016/s1350-4177(99)00036-x.

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17

Atobe, Mahito, Michiaki Sasahira, and Tsutomu Nonaka. "Ultrasonic effects on electroorganic processes." Ultrasonics Sonochemistry 7, no. 3 (July 2000): 103–7. http://dx.doi.org/10.1016/s1350-4177(99)00044-9.

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18

Pletcher, Derek. "Novel trends in electroorganic synthesis." Journal of Electroanalytical Chemistry 422, no. 1-2 (February 1997): 201. http://dx.doi.org/10.1016/s0022-0728(97)80113-1.

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19

Grimshaw, James. "Recent advances in electroorganic synthesis." Electrochimica Acta 33, no. 9 (September 1988): 1255. http://dx.doi.org/10.1016/0013-4686(88)80160-9.

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20

Bouzek, Karel, Vladimír Jiřičný, Roman Kodým, Jiří Křišťál, and Tomáš Bystroň. "Microstructured reactor for electroorganic synthesis." Electrochimica Acta 55, no. 27 (November 2010): 8172–81. http://dx.doi.org/10.1016/j.electacta.2010.05.061.

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21

Atobe, Mahito, Naohiro Yamada, Toshio Fuchigami, and Tsutomu Nonaka. "Ultrasonic effects on electroorganic processes." Electrochimica Acta 48, no. 12 (May 2003): 1759–66. http://dx.doi.org/10.1016/s0013-4686(03)00153-1.

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22

Cignitti, M. "Recent Advances in Electroorganic Synthesis." Bioelectrochemistry and Bioenergetics 19, no. 1 (March 1988): 187–88. http://dx.doi.org/10.1016/0302-4598(88)85026-8.

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23

Pletcher, D. "Emerging Opportunities for Electroorganic Processes." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 195, no. 2 (November 1985): 439. http://dx.doi.org/10.1016/0022-0728(85)80065-6.

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24

Hasegawa, Masaru, and Toshio Fuchigami. "Electroorganic reactions in ionic liquids." Electrochimica Acta 49, no. 20 (August 2004): 3367–72. http://dx.doi.org/10.1016/j.electacta.2004.03.015.

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25

Chaloner, Penny A. "Electroorganic Synthesis; Best synthetic Methods." Journal of Organometallic Chemistry 418, no. 1 (October 1991): C17—C18. http://dx.doi.org/10.1016/0022-328x(91)86358-w.

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26

Atobe, Mahito, Naohiro Yamada, and Tsutomu Nonaka. "Ultrasonic effects on electroorganic processes." Electrochemistry Communications 1, no. 11 (November 1999): 532–35. http://dx.doi.org/10.1016/s1388-2481(99)00111-3.

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27

MAKI, Shojiro, and Haruki NIWA. "The Application of Electroorganic Chemical Reaction." Journal of Synthetic Organic Chemistry, Japan 56, no. 9 (1998): 725–35. http://dx.doi.org/10.5059/yukigoseikyokaishi.56.725.

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28

Takahashi, Machiko, Masato Fujita, and Masatoki Ito. "SERS application to some electroorganic reactions." Surface Science Letters 158, no. 1-3 (July 1985): A424. http://dx.doi.org/10.1016/0167-2584(85)90023-4.

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29

Horcajada, Roberto, Masayuki Okajima, Seiji Suga, and Jun-ichi Yoshida. "Microflow electroorganic synthesis without supporting electrolyte." Chemical Communications, no. 10 (2005): 1303. http://dx.doi.org/10.1039/b417388k.

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30

Takahashi, Machiko, Masato Fujita, and Masatoki Ito. "SERS application to some electroorganic reactions." Surface Science 158, no. 1-3 (July 1985): 307–13. http://dx.doi.org/10.1016/0039-6028(85)90305-x.

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31

Ogawa, Kelli A., and Andrew J. Boydston. "Recent Developments in Organocatalyzed Electroorganic Chemistry." Chemistry Letters 44, no. 1 (January 5, 2015): 10–16. http://dx.doi.org/10.1246/cl.140915.

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32

Baizer, M. M. "Electroorganic processes practiced in the world." Pure and Applied Chemistry 58, no. 6 (January 1, 1986): 889–94. http://dx.doi.org/10.1351/pac198658060889.

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33

Nguyen, Zachary A., Dylan Boucher, and Shelley D. Minteer. "Electrolyte Induced Solvent Cage Effects for Enantioselective Electrosynthesis." ECS Meeting Abstracts MA2022-02, no. 53 (October 9, 2022): 2514. http://dx.doi.org/10.1149/ma2022-02532514mtgabs.

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Electrochemistry provides a tunable, regioselective, and green alternative to traditional synthetic organic methods, and access to reactive intermediates. Problematically, electrochemical redox events often go through planar radical intermediates, thus destroying enantioselectivity. As such, researchers have sought the “chiral electron”, a general methodology to impart enantioselectivity to electroorganic reactions. One strategy has been asymmetric transition metal catalysis while replacing the typical stochiometric redox reagent needed with electricity, thus providing a chiral pathway for elecoorganic reactions. However, the general physical parameters that govern enantioselectivity at electrochemical interfaces, remains poorly understood. Here, we focus on the effects of supporting electrolyte in synthetic organic electrochemistry, specifically its role in enantioselective reactions. Cyclic voltammetry provides a tool to investigate the mechanistic consequences of changes in electrolyte. Using the model reaction of enantioselective carboxylation with a cobalt catalyst, we observe changes in mechanism as the electrolyte size is varied. Specifically, electrolyte identity effects the lifetime of the chiral Co-alkyl intermediate. These fundamental electroanalytical studies provide a sound mechanistic basis for the origin of enantioselectivity in electroorganic reactions. In summary, these results of a general interest as a strategy to tune and improve enantioselectivity in electrochemical transformations.
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34

Beil, Sebastian B., Dennis Pollok, and Siegfried R. Waldvogel. "Reproducibility in Electroorganic Synthesis—Myths and Misunderstandings." Angewandte Chemie International Edition 60, no. 27 (March 3, 2021): 14750–59. http://dx.doi.org/10.1002/anie.202014544.

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35

Regenbrecht, Carolin, and Siegfried R. Waldvogel. "Efficient electroorganic synthesis of 2,3,6,7,10,11-hexahydroxytriphenylene derivatives." Beilstein Journal of Organic Chemistry 8 (October 10, 2012): 1721–24. http://dx.doi.org/10.3762/bjoc.8.196.

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2,3,6,7,10,11-Hexahydroxytriphenylene of good quality and purity can be obtained via anodic treatment of catechol ketals and subsequent acidic hydrolysis. The electrolysis is conducted in propylene carbonate circumventing toxic and expensive acetonitrile. The protocol is simple to perform and superior to other chemical or electrochemical methods. The key of the method is based on the low solubility of the anodically trimerized product. The shift of potentials is supported by cyclic voltammetry studies.
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36

SHONO, Tatsuya. "Electroorganic chemistry in organic synthesis. General survey." Journal of Synthetic Organic Chemistry, Japan 43, no. 6 (1985): 491–95. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.491.

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37

FUCHIGAMI, Toshio. "Selective Electroorganic Reactions Using Transition Metal Complexes." Journal of Japan Oil Chemists' Society 39, no. 10 (1990): 888–94. http://dx.doi.org/10.5650/jos1956.39.10_888.

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38

Gütz, Christoph, Andreas Stenglein, and Siegfried R. Waldvogel. "Highly Modular Flow Cell for Electroorganic Synthesis." Organic Process Research & Development 21, no. 5 (May 4, 2017): 771–78. http://dx.doi.org/10.1021/acs.oprd.7b00123.

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39

Bellamy, A. J. "Electroorganic synthesis Festschriff for Manuel M. Baizer." Electrochimica Acta 39, no. 1 (January 1994): 158. http://dx.doi.org/10.1016/0013-4686(94)85028-3.

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40

Guetz, Christoph, Bernhard Kloeckner, and Siegfried R. Waldvogel. "ChemInform Abstract: Electrochemical Screening for Electroorganic Synthesis." ChemInform 47, no. 11 (February 2016): no. http://dx.doi.org/10.1002/chin.201611252.

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41

TORII, S. "ChemInform Abstract: Organometal Complexes in Electroorganic Synthesis." ChemInform 25, no. 13 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199413303.

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42

NONAKA, Tsutomu, and Toshio FUCHIGAMI. "Modified electrodes and their applications to electroorganic reactions." Journal of Synthetic Organic Chemistry, Japan 43, no. 6 (1985): 565–74. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.565.

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43

NISHIGUCHI, Ikuzo. "Experimental methods for electroorganic synthesis in a laboratory." Journal of Synthetic Organic Chemistry, Japan 43, no. 6 (1985): 617–33. http://dx.doi.org/10.5059/yukigoseikyokaishi.43.617.

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44

HISAEDA, Yoshio. "Electroorganic Reactions Mediated by Vitamin B12 Model Complexes." Journal of Synthetic Organic Chemistry, Japan 54, no. 10 (1996): 859–67. http://dx.doi.org/10.5059/yukigoseikyokaishi.54.859.

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45

Rauen, Anna Lisa, Frank Weinelt, and Siegfried R. Waldvogel. "Sustainable electroorganic synthesis of lignin-derived dicarboxylic acids." Green Chemistry 22, no. 18 (2020): 5956–60. http://dx.doi.org/10.1039/d0gc02210a.

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46

KASHIWAGI, Yoshitomo. "Construction of Functional Electrode Interface for Electroorganic Synthesis." YAKUGAKU ZASSHI 127, no. 7 (July 1, 2007): 1047–57. http://dx.doi.org/10.1248/yakushi.127.1047.

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47

Navarro, Marcelo. "Recent advances in experimental procedures for electroorganic synthesis." Current Opinion in Electrochemistry 2, no. 1 (April 2017): 43–52. http://dx.doi.org/10.1016/j.coelec.2017.03.004.

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48

Thomas, F. B., P. A. Ramachandran, M. P. Dudukovic, and R. E. W. Jansson. "Laminar radial flow electrochemical reactors. III. Electroorganic sysnthesis." Journal of Applied Electrochemistry 19, no. 6 (November 1989): 856–67. http://dx.doi.org/10.1007/bf01007933.

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49

Nishiguchi, Ikuzo. "Some Progress and Development on Synthetic Electroorganic Chemistry." ECS Transactions 2, no. 22 (December 21, 2019): 19–24. http://dx.doi.org/10.1149/1.2409000.

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50

Pragst, F., and M. Niazymbetov. "Electrogenerated chemiluminescence in mechanistic investigations of electroorganic reactions." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 197, no. 1-2 (January 1986): 245–64. http://dx.doi.org/10.1016/0022-0728(86)80153-x.

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