4 Electroreductive Reactions
Book
Editor: Ackermann, L.
Title: Electrochemistry in Organic Synthesis
Print ISBN: 9783132442122; Online ISBN: 9783132442146; Book DOI: 10.1055/b000000126
1st edition © 2022. Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry
Science of Synthesis Reference Libraries
Parent publication
Title: Science of Synthesis
DOI: 10.1055/b-00000101
Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Type: Multivolume Edition
Abstract
This review covers a variety of electroreductive reactions. A range of catalyzed electroreductive cross-coupling reactions, electroreduction of various functional groups and carbon dioxide, decarboxylation reactions, and oxygen reduction reactions are discussed.
Key words
organic electrochemistry - electrosynthesis - nickel catalysts - cobalt catalysts - iron catalysts - electrochemical reduction - cross-coupling reactions - reductive coupling - carboxylation - decarboxylation - carbon dioxide - molecular oxygen- 1 Wiebe A, Gieshoff T, Möhle S, Rodrigo E, Zirbes M, Waldvogel SR. Angew. Chem. Int. Ed. 2018; 57: 5594
- 11 Kumar GS, Peshkov A, Brzozowska A, Nikolaienko P, Zhu C, Rueping M. Angew. Chem. Int. Ed. 2020; 59: 6513
- 12 Fauvarque J.-F, Petit M.-A, Pfluger F, Jutand A, Chevrot C, Troupel M. Macromol. Rapid Commun. 1983; 4: 455
- 55 Yang L, Huang Z, Li G, Zhang W, Cao R, Wang C, Xiao J, Xue D. Angew. Chem. Int. Ed. 2018; 57: 1968
- 56 Zou Y.-Q, Chen J.-R, Liu X.-P, Lu L.-Q, Davis RL, Jørgensen KA, Xiao W.-J. Angew. Chem. Int. Ed. 2012; 51: 784
- 57 Chandrasekaran M, Noel M, Krishnan V. J. Electroanal. Chem. Interfacial Electrochem. 1991; 303: 185
- 58 Cantu DC, Padmaperuma AB, Nguyen M.-T, Akhade SA, Yoon Y, Wang Y.-G, Lee M.-S, Glezakou V.-A, Rousseau R, Lilga MA. ACS Catal. 2018; 8: 7645
- 62 Grigorʼev IA, In: Nitrile Oxides, Nitrones, and Nitronates in Organic Synthesis: Novel Strategies in Synthesis Feuer H. John Wiley & Sons Hoboken, NJ 2007; 129-464
- 70 López-López EE, Pérez-Bautista JA, Sartillo-Piscil F, Frontana-Uribe BA. Beilstein J. Org. Chem. 2018; 14: 547
- 91 Medvedev JJ, Medvedeva XV, Li F, Zienchuk TA, Klinkova A. ACS Sustainable Chem. Eng. 2019; 7: 19631
- 93 Maag H, In: Prodrugs: Challenges and Rewards Stella V, Borchardt R, Hageman M, Oliyai R, Maag H, Tilley J. Springer 2007; 703
- 94 Adamian VA, Gong WH, In: Liquid Phase Aerobic Oxidation Catalysis: Industrial Applications and Academic Perspectives Stahl SS, Alsters PL. Wiley-VCH Weinheim, Germany 2016; 41
- 95 Saltmarsh M, Insall L, In: Essential Guide to Food Additives Saltmarsh M. RSC Publishing Cambridge 2013; 1
- 100 Procter DJ, Flowers II RA, Skrydstrup T. Organic Synthesis Using Samarium Diiodide: A Practical Guide. RSC Publishing; Cambridge 2009
-
110 Jiao K.-J, Li Z.-M, Xu X.-T, Zhang L.-P, Li Y.-Q, Zhang K, Mei T.-S. Org. Chem. Front. 2018; 5: 2244
- 112 Gooyit M, Song W, Mahasenan KV, Lichtenwalter K, Suckow MA, Schroeder VA, Wolter WR, Mobashery S, Chang M. J. Med. Chem. 2013; 56: 8139
- 128 Zuo Z, Ahneman DT, Chu L, Terrett JA, Doyle AG, MacMillan DWC. Science (Washington, D. C.) 2014; 345: 437
- 130 Xiang J, Shang M, Kawamata Y, Lundberg H, Reisberg SH, Chen M, Mykhailiuk P, Beutner G, Collins MR, Davies A, Del Bel M, Gallego GM, Spangler JE, Starr J, Yang S, Blackmond DG, Baran PS. Nature (London) 2019; 573: 398
- 137 Fawcett A, Pradeilles J, Wang Y, Mutsuga T, Myers EL, Aggarwal VK. Science (Washington, D. C.) 2017; 357: 283
- 141 Metal-Catalyzed Cross-Coupling Reactions. Diederich F, Stang PJ. Wiley VCH; Weinheim, Germany 1998
- 144 Tellis JC, Kelly CB, Primer DN, Jouffroy M, Patel NR, Molander GA. Acc. Chem. Res. 2016; 49: 1429
- 156 Liu Y, Xue L, Shi B, Bu F, Wang D, Lu L, Shi R, Lei A. Chem. Commun. (Cambridge) 2019; 55: 14922
- 158 Koyanagi T, Herath A, Chong A, Ratnikov M, Valiere A, Chang J, Molteni V, Loren J. Org. Lett. 2019; 21: 816
- 170 Stamenkovic VR, Mun BS, Arenz M, Mayrhofer KJJ, Lucas CA, Wang G, Ross PN, Markovic NM. Nat. Mater. 2007; 6: 241
- 171 Greeley J, Stephens IEL, Bondarenko AS, Johansson TP, Hansen HA, Jaramillo TF, Rossmeisl J, Chorkendorff I, Nørskov JK. Nat. Chem. 2009; 1: 552
- 172 Dagani MJ, Barda HJ, Benya TJ, Sanders DC In: Ullmannʼs Encyclopedia of Industrial Chemistry: Bromine Compounds Wiley-VCH Weinheim, Germany 2000;
- 174 Tian S, Lv S, Jia X, Ma L, Li B, Zhang G, Gao W, Wei Y, Chen J. Adv. Synth. Catal. 2019; 361: 5626
- 175 Tian S, Jia X, Wang L, Li B, Liu S, Ma L, Gao W, Wei Y, Chen J. Chem. Commun. (Cambridge) 2019; 55: 12104