Ackermann, L. : 2022 Science of Synthesis, 2021/5: Electrochemistry in Organic Synthesis DOI: 10.1055/sos-SD-236-00075
Electrochemistry in Organic Synthesis

4 Electroreductive Reactions

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Book

Editor: Ackermann, L.

Authors: Ackermann, L. ; Brown, R. C. D. ; Enders, P.; Fang, P.; Folgueiras-Amador, A. A. ; Francke, R. ; Galczynski, J.; Gosmini, C. ; Hodgson, J. W.; Hou, Z.-W.; Huang, H.; Huang, Z.; Inagi, S. ; Kuciński, K. ; Kuriyama, M. ; Lam, K. ; Lambert, T. H.; Leech, M. C. ; Lennox, A. J. J. ; Lin, Z.; Little, R. D.; Massignan, L.; Mei, T.-S.; Meyer, T. H.; Moeller, K. D. ; Onomura, O. ; Prudlik, A.; Ruan, Z. ; Scheremetjew, A. ; Schiltz, P.; Selt, M.; Villani, E. ; Waldvogel, S. R. ; Wang, Z.-H.; Wu, T.; Xing, Y.-K.; Xu, H.-C. ; Yamamoto, K.

Title: Electrochemistry in Organic Synthesis

Print ISBN: 9783132442122; Online ISBN: 9783132442146; Book DOI: 10.1055/b000000126

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.

 
  • 1 Wiebe A, Gieshoff T, Möhle S, Rodrigo E, Zirbes M, Waldvogel SR. Angew. Chem. Int. Ed. 2018; 57: 5594
  • 2 Shatskiy A, Lundberg H, Kärkäs MD. ChemElectroChem 2019; 6: 4067
  • 3 Yan M, Kawamata Y, Baran PS. Chem. Rev. 2017; 117: 13230
  • 4 Ghosh M, Shinde VS, Rueping M. Beilstein J. Org. Chem. 2019; 15: 2710
  • 5 Durandetti M, Périchon J. Synthesis 2004; 3079
  • 6 Durandetti M, Nédélec J.-Y, Périchon J. J. Org. Chem. 1996; 61: 1748
  • 7 Durandetti M, Périchon J, Nédélec J.-Y. J. Org. Chem. 1997; 62: 7914
  • 8 DeLano TJ, Reisman SE. ACS Catal. 2019; 9: 6751
  • 9 Perkins RJ, Pedro DJ, Hansen EC. Org. Lett. 2017; 19: 3755
  • 10 Perkins RJ, Hughes AJ, Weix DJ, Hansen EC. Org. Process Res. Dev. 2019; 23: 1746
  • 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
  • 13 Torii S, Tanaka H, Morisaki K. Tetrahedron Lett. 1985; 26: 1655
  • 14 Amatore C, Jutand A. Organometallics 1988; 7: 2203
  • 15 Amatore C, Carré E, Jutand A, Tanaka H, Ren Q, Torii S. Chem.–Eur. J. 1996; 2: 957
  • 16 Courtois V, Barhdadi R, Troupel M, Périchon J. Tetrahedron 1997; 53: 11569
  • 17 Courtois V, Barhdadi R, Condon S, Troupel M. Tetrahedron Lett. 1999; 40: 5993
  • 18 Troupel M, Rollin Y, Sibille S, Périchon J, Fauvarque J.-F. J. Organomet. Chem. 1980; 202: 435
  • 19 Mori M, Hashimoto Y, Ban Y. Tetrahedron Lett. 1980; 21: 631
  • 20 Schiavon G, Bontempelli G, Corain B. J. Chem. Soc., Dalton Trans. 1981; 1074
  • 21 Rollin Y, Troupel M, Tuck DG, Périchon J. J. Organomet. Chem. 1986; 303: 131
  • 22 Meyer G, Rollin Y, Périchon J. J. Organomet. Chem. 1987; 333: 263
  • 23 Raynal F, Barhdadi R, Périchon J, Savall A, Troupel M. Adv. Synth. Catal. 2002; 344: 45
  • 24 Gosmini C, Nédélec JY, Périchon J. Tetrahedron Lett. 2000; 41: 201
  • 25 Gosmini C, Nédélec JY, Périchon J. Tetrahedron Lett. 2000; 41: 5039
  • 26 Gosmini C, Lasry S, Nédélec J.-Y, Périchon J. Tetrahedron 1998; 54: 1289
  • 27 Cannes C, Labbé E, Durandetti M, Devaud M, Nédélec JY. J. Electroanal. Chem. 1996; 412: 85
  • 28 Cannes C, Condon S, Durandetti M, Périchon J, Nédélec J.-Y. J. Org. Chem. 2000; 65: 4575
  • 29 Durandetti M, Périchon J, Nédélec J.-Y. Tetrahedron Lett. 1999; 40: 9009
  • 30 Durandetti M, Nédélec J.-Y, Périchon J. Org. Lett. 2001; 3: 2073
  • 31 Amatore C, Jutand A, Périchon J, Rollin Y. Monatsh. Chem. 2000; 131: 1293
  • 32 Perlmutter P. Conjugate Addition Reactions in Organic Synthesis. Pergamon; New York 1992
  • 33 Condon S, Dupré D, Falgayrac G, Nédélec J.-Y. Eur. J. Org. Chem. 2002; 105
  • 34 Condon S, Nédélec J.-Y. Synthesis 2004; 3070
  • 35 Condon S, Dupré D, Lachaise I, Nédélec J.-Y. Synthesis 2002; 1752
  • 36 Condon-Gueugnot S, Dupré D, Nédélec J.-Y, Périchon J. Synthesis 1997; 1457
  • 37 Condon S, Dupré D, Nédélec JY. Org. Lett. 2003; 5: 4701
  • 38 Buriez O, Cannes C, Nédélec J.-Y, Périchon J. J. Electroanal. Chem. 2000; 495: 57
  • 39 Buriez O, Nédélec J.-Y, Périchon J. J. Electroanal. Chem. 2001; 506: 162
  • 40 Gosmini C, Rollin Y, Nédélec JY, Périchon J. J. Org. Chem. 2000; 65: 6024
  • 41 Gomes P, Gosmini C, Périchon J. J. Org. Chem. 2003; 68: 1142
  • 42 Gomes P, Buriez O, Labbé E, Gosmini C, Périchon J. J. Electroanal. Chem. 2004; 562: 255
  • 43 Gomes P, Gosmini C, Nédélec J.-Y, Périchon J. Tetrahedron Lett. 2002; 43: 5901
  • 44 Le Gall E, Gosmini C, Nédélec J.-Y, Périchon J. Tetrahedron Lett. 2001; 42: 267
  • 45 Gomes P, Gosmini C, Périchon J. Tetrahedron 2003; 59: 2999
  • 46 Polleux L, Labbé E, Buriez O, Périchon J. Chem.–Eur. J. 2005; 11: 4678
  • 47 Gomes P, Gosmini C, Nédélec J.-Y, Périchon J. Tetrahedron Lett. 2000; 41: 3385
  • 48 Condon S, Cannes C, Bedioui F. J. Chem. 2019; 9832 639
  • 49 Chaussard J, Folest JC, Nédélec JY, Périchon J, Sibille S, Troupel M. Synthesis 1990; 369
  • 50 Durandetti M, Meignein C, Périchon J. Org. Lett. 2003; 5: 317
  • 51 Durandetti M, Meignein C, Périchon J. J. Org. Chem. 2003; 68: 3121
  • 52 Bartoli G, Bartolacci M, Giuliani A, Marcantoni E, Massaccesi M. Eur. J. Org. Chem. 2005; 2867
  • 53 Nakamura K, Matsuda T. Curr. Org. Chem. 2006; 10: 1217
  • 54 Shende VS, Singh P, Bhanage BM. Catal. Sci. Technol. 2018; 8: 955
  • 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
  • 59 Eseyin AE, Steele PH. Int. J. Adv. Chem. 2015; 3: 6
  • 60 Wang Y, Zhao D, Rodríguez-Padrón D, Len C. Catalysts 2019; 9: 796
  • 61 Cao Y, Noël T. Org. Process Res. Dev. 2019; 23: 403
  • 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
  • 63 Radivoy G, Radivoy G, Alonso F, Yus M. Synthesis 2001; 427
  • 64 Formenti D, Ferretti F, Scharnagl FK, Beller M. Chem. Rev. 2019; 119: 2611
  • 65 Rodrigo E, Waldvogel SR. Chem. Sci. 2019; 10: 2044
  • 66 Shundrina IK, Odintsov DS, Osʼkina IA, Irtegova IG, Shundrin LA. Eur. J. Org. Chem. 2018; 3471
  • 67 Rodrigo E, Baunis H, Suna E, Waldvogel SR. Chem. Commun. (Cambridge) 2019; 55: 12255
  • 68 Corey EJ, Winter RAE. J. Am. Chem. Soc. 1963; 85: 2677
  • 69 Corey EJ, Carey FA, Winter RAE. J. Am. Chem. Soc. 1965; 87: 934
  • 70 López-López EE, Pérez-Bautista JA, Sartillo-Piscil F, Frontana-Uribe BA. Beilstein J. Org. Chem. 2018; 14: 547
  • 71 Omae I. Coord. Chem. Rev. 2012; 256: 1384
  • 72 Pletcher D. Electrochem. Commun. 2015; 61: 97
  • 73 von der Assen N, Voll P, Peters M, Bardow A. Chem. Soc. Rev. 2014; 43: 7982
  • 74 Bobbink FD, Menoud F, Dyson PJ. ACS Sustainable Chem. Eng. 2018; 6: 12119
  • 75 Omae I. Catal. Today 2006; 115: 33
  • 76 Kleij AW, North M, Urakawaurea A. ChemSusChem 2017; 10: 1036
  • 77 Honda M, Tamura M, Nakagawa Y, Tomishige K. Catal. Sci. Technol. 2014; 4: 2830
  • 78 Tappe NA, Reich RM, DʼElia V, Kühn FE. Dalton Trans. 2018; 47: 13281
  • 79 Liu Y, Ren W.-M, He K.-K, Zhang W.-Z, Li W.-B, Wang M, Lu X.-B. J. Org. Chem. 2016; 81: 8959
  • 80 Ren Y, Rousseaux SAL. J. Org. Chem. 2018; 83: 913
  • 81 Alper E, Orhan OY. Petroleum 2017; 3: 109
  • 82 Fauvarque J.-F, Jutand A, Francois M. J. Appl. Electrochem. 1988; 18: 109
  • 83 Tokuda M. J. Nat. Gas Chem. 2006; 15: 275
  • 84 Matthessen R, Fransaer J, Binnemans K, De Vos DE. Beilstein J. Org. Chem. 2014; 10: 2484
  • 85 Krase NW, Gaddy VL. Ind. Eng. Chem. 1922; 14: 611
  • 86 Correa A, Martín R. Angew. Chem. Int. Ed. 2009; 48: 6201
  • 87 Senboku H, Katayama A. Curr. Opin. Green Sustainable Chem. 2017; 3: 50
  • 88 León T, Correa A, Martín R. J. Am. Chem. Soc. 2013; 135: 1221
  • 89 del Olmo A, Calzada J, Nuñez M. Crit. Rev. Food Sci. Nutr. 2017; 57: 3084
  • 90 Nair B. Int. J. Toxicol. 2001; 20: 23
  • 91 Medvedev JJ, Medvedeva XV, Li F, Zienchuk TA, Klinkova A. ACS Sustainable Chem. Eng. 2019; 7: 19631
  • 92 Bazzi S, Le Duc G, Schulz E, Gosmini C, Mellah M. Org. Biomol. Chem. 2019; 17: 8546
  • 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
  • 96 Franklin AS. J. Chem. Soc., Perkin Trans. 1 1998; 2451
  • 97 Wu X.-F, Zheng F. Top. Curr. Chem. 2016; 375: 4
  • 98 Huang K, Sun C.-L, Shi Z.-J. Chem. Soc. Rev. 2011; 40: 2435
  • 99 Leucio R. Curr. Green Chem. 2015; 2: 77
  • 100 Procter DJ, Flowers II RA, Skrydstrup T. Organic Synthesis Using Samarium Diiodide: A Practical Guide. RSC Publishing; Cambridge 2009
  • 101 Bazzi S, Schulz E, Mellah M. Org. Lett. 2019; 21: 10033
  • 102 Wu L.-X, Sun Q.-L, Yang M.-P, Zhao Y.-G, Guan Y.-B, Wang H, Lu J.-X. Catalysts 2018; 8: 273
  • 103 Damodar J, Krishna Mohan S, Khaja Lateef SK, Jayarama Reddy S. Synth. Commun. 2005; 35: 1143
  • 104 Mena S, Sanchez J, Guirado G. RSC Adv. 2019; 9: 15115
  • 105 Ouyang K, Hao W, Zhang W.-X, Xi Z. Chem. Rev. 2015; 115: 12045
  • 106 Yang D.-T, Zhu M, Schiffer ZJ, Williams K, Song X, Liu X, Manthiram K. ACS Catal. 2019; 9: 4699
  • 107 Poterała M, Dranka M, Borowiecki P. Eur. J. Org. Chem. 2017; 2290
  • 108 Senboku H, Sakai K, Fukui A, Sato Y, Yamauchi Y. ChemElectroChem 2019; 6: 4158
  • 109 Moragas T, Cornella J, Martin R. J. Am. Chem. Soc. 2014; 136: 17702
  • 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
  • 111 Bowman WR, Bridge CF, Brookes P. J. Chem. Soc., Perkin Trans. 1 2000; 1
  • 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
  • 113 Divito CB, Davies S, Masoudi S, Muhoro CN. J. Agric. Food Chem. 2007; 55: 5377
  • 114 Salisaeng P, Arnnok P, Patdhanagul N, Burakham R. J. Agric. Food Chem. 2016; 64: 2145
  • 115 Wang J, Qian P, Hu K, Zha Z, Wang Z. ChemElectroChem 2019; 6: 4292
  • 116 Singh PK, Silakari O. ChemMedChem 2018; 13: 1071
  • 117 Kumar D, Jain SK. Curr. Med. Chem. 2016; 23: 4338
  • 118 Katayama A, Senboku H. ChemElectroChem 2016; 3: 2052
  • 119 Katayama A, Senboku H, Hara S. Tetrahedron 2016; 72: 4626
  • 120 Patra T, Maiti D. Chem.–Eur. J. 2017; 23: 7382
  • 121 Kolbe H. Justus Liebigs Ann. Chem. 1849; 69: 257
  • 122 Faraday M. Philos. Trans. R. Soc. London 1832; 125
  • 123 Leech MC, Lam K. Acc. Chem. Res. 2020; 53: 121
  • 124 Chen X, Luo X, Peng X, Guo J, Zai J, Wang P. Chem.–Eur. J. 2020; 26: 3226
  • 125 Weaver JD, Recio A, Grenning AJ, Tunge JA. Chem. Rev. 2011; 111: 1846
  • 126 Wei Y, Hu P, Zhang M, Su W. Chem. Rev. 2017; 117: 8864
  • 127 Johnston CP, Smith RT, Allmendinger S, MacMillan DWC. Nature (London) 2016; 536: 322
  • 128 Zuo Z, Ahneman DT, Chu L, Terrett JA, Doyle AG, MacMillan DWC. Science (Washington, D. C.) 2014; 345: 437
  • 129 Chu L, Ohta C, Zuo Z, MacMillan DWC. J. Am. Chem. Soc. 2014; 136: 10886
  • 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
  • 131 Goossen LJ, Collet F, Goossen K. Isr. J. Chem. 2010; 50: 617
  • 132 Schäfer HJ. Chem. Phys. Lipids 1979; 24: 321
  • 133 Schäfer HJ. Angew. Chem. Int. Ed. Engl. 1981; 20: 911
  • 134 Utley J. Chem. Soc. Rev. 1997; 26: 157
  • 135 Murarka S. Adv. Synth. Catal. 2018; 360: 1735
  • 136 Jin Y, Fu H. Asian J. Org. Chem. 2017; 6: 368
  • 137 Fawcett A, Pradeilles J, Wang Y, Mutsuga T, Myers EL, Aggarwal VK. Science (Washington, D. C.) 2017; 357: 283
  • 138 Guo J.-Y, Zhang Z.-Y, Guan T, Mao L.-W, Ban Q, Zhao K, Loh T.-P. Chem. Sci. 2019; 10: 8792
  • 139 Cheng W.-M, Shang R, Fu M.-C, Fu Y. Chem.–Eur. J. 2017; 23: 2537
  • 140 Lyu X.-L, Huang S.-S, Song H.-J, Liu Y.-X, Wang Q.-M. Org. Lett. 2019; 21: 5728
  • 141 Metal-Catalyzed Cross-Coupling Reactions. Diederich F, Stang PJ. Wiley VCH; Weinheim, Germany 1998
  • 142 Jana R, Pathak TP, Sigman MS. Chem. Rev. 2011; 111: 1417
  • 143 Tasker SZ, Standley EA, Jamison TF. Nature (London) 2014; 509: 299
  • 144 Tellis JC, Kelly CB, Primer DN, Jouffroy M, Patel NR, Molander GA. Acc. Chem. Res. 2016; 49: 1429
  • 145 Fu GC. ACS Cent. Sci. 2017; 3: 692
  • 146 Twilton J, Le C, Zhang P, Shaw MH, Evans RW, MacMillan DWC. Nat. Rev. Chem. 2017; 1: 0052
  • 147 Weix DJ. Acc. Chem. Res. 2015; 48: 1767
  • 148 Everson DA, Shrestha R, Weix DJ. J. Am. Chem. Soc. 2010; 132: 920
  • 149 Wang X, Wang S, Xue W, Gong H. J. Am. Chem. Soc. 2015; 137: 11562
  • 150 Eberhardt NA, Guan H. Chem. Rev. 2016; 116: 8373
  • 151 Zimmermann P, Limberg C. J. Am. Chem. Soc. 2017; 139: 4233
  • 152 Zhang S.-K, Samanta RC, Del Vecchio A, Ackermann L. Chem.–Eur. J. 2020; 26: 10936
  • 153 Schwarz J, König B. Green Chem. 2016; 18: 4743
  • 154 Zheng C, Wang G.-Z, Shang R. Adv. Synth. Catal. 2019; 361: 4500
  • 155 Lian F, Xu K, Meng W, Zhang H, Tan Z, Zeng C. Chem. Commun. (Cambridge) 2019; 55: 14685
  • 156 Liu Y, Xue L, Shi B, Bu F, Wang D, Lu L, Shi R, Lei A. Chem. Commun. (Cambridge) 2019; 55: 14922
  • 157 Li H, Breen CP, Seo H, Jamison TF, Fang Y.-Q, Bio MM. Org. Lett. 2018; 20: 1338
  • 158 Koyanagi T, Herath A, Chong A, Ratnikov M, Valiere A, Chang J, Molteni V, Loren J. Org. Lett. 2019; 21: 816
  • 159 Jackson A, Meth-Cohn O. J. Chem. Soc., Chem. Commun. 1995; 1319
  • 160 Gerack CJ, McElwee-White L. Molecules 2014; 19: 7689
  • 161 Lin D.-Z, Huang J.-M. Org. Lett. 2018; 20: 2112
  • 162 Jiao Y, Zheng Y, Jaroniec M, Qiao SZ. Chem. Soc. Rev. 2015; 44: 2060
  • 163 Barkholtz HM, Liu D.-J. Mater. Horiz. 2017; 4: 20
  • 164 Zhang P, Zhao Y, Zhang X. Chem. Soc. Rev. 2018; 47: 2921
  • 165 Davari E, Ivey DG. Sustainable Energy Fuels 2018; 2: 39
  • 166 Nosaka Y, Nosaka AY. Chem. Rev. 2017; 117: 11302
  • 167 Han X, Wang K, Zhang G, Gao W, Chen J. Adv. Synth. Catal. 2019; 361: 2804
  • 168 Hayyan M, Hashim MA, AlNashef IM. Chem. Rev. 2016; 116: 3029
  • 169 Zhang L, Ji X, Wang X, Fu Y, Zhu H, Liu TX. J. Electrochem. Soc. 2020; 167: 024507
  • 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;
  • 173 Erian AW, Sherif SM, Gaber HM. Molecules 2003; 8: 793
  • 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
  • 176 Janeczko M, Demchuk OM, Strzelecka D, Kubiński K, Masłyk M. Eur. J. Med. Chem. 2016; 124: 1019
  • 177 Prati F, Bergamini C, Molina MT, Falchi F, Cavalli A, Kaiser M, Brun R, Fato R, Bolognesi ML. J. Med. Chem. 2015; 58: 6422
  • 178 Barba F, Batanero B, Barba I. J. Electroanal. Chem. 2017; 793: 66
  • 179 Dunetz JR, Magano J, Weisenburger GA. Org. Process Res. Dev. 2016; 20: 140
  • 180 Crozet D, Urrutigoïty M, Kalck P. ChemCatChem 2011; 3: 1102
  • 181 Patil MD, Grogan G, Bommarius A, Yun H. ACS Catal. 2018; 8: 10985
  • 182 Pandolfi F, Chiarotto I, Rocco D, Feroci M. Electrochim. Acta 2017; 254: 358
  • 183 Rocco D, Chiarotto I, Mattiello L, Pandolfi F, Zane D, Feroci M. Pure Appl. Chem. 2019; 91: 1709