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Ackermann, L. : 2022 Science of Synthesis, 2021/5: Electrochemistry in Organic Synthesis DOI: 10.1055/sos-SD-236-00213
Electrochemistry in Organic Synthesis

11 Electrophotocatalysis

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Herausgeber: Ackermann, L. 

Autoren: 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. 

Titel: Electrochemistry in Organic Synthesis

Print ISBN: 9783132442122; Online ISBN: 9783132442146; Buch-DOI: 10.1055/b000000126

1st edition © 2022. Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart

Fachgebiete: Organische Chemie;Chemische Reaktionen, Katalyse;Organometallchemie;Chemische Labormethoden, Stöchiometrie

Science of Synthesis Reference Libraries



Übergeordnete Publikation

Titel: Science of Synthesis

DOI: 10.1055/b-00000101

Reihenherausgeber: 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.

Typ: Mehrbändiges Werk

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Abstract

Electrocatalysis and photocatalysis have proven to be powerful strategies for molecular synthesis. Recently, methods that combine the power of light and electricity within a single catalyst have been reported. This area, termed electrophotocatalysis, offers new opportunities to promote challenging transformations. This chapter covers recent work in this area and demonstrates some of the possibilities offered by these approaches for rapidly constructing complex structures through the merger of electrochemical and photochemical energy.

Schlüsselwörter

organic electrochemistry - electrosynthesis - photochemistry - catalysis - redox chemistry
 
  • 1 Yoshida J.-i, Kataoka K, Horcajada R, Nagaki A. Chem. Rev. 2008; 108: 2265
    PubMed
  • 2 Francke R, Little RD. Chem. Soc. Rev. 2014; 43: 2492
    PubMed
  • 3 Yan M, Kawamata Y, Baran PS. Chem. Rev. 2017; 117: 13230
    PubMed
  • 4 Moeller KD. Chem. Rev. 2018; 118: 4817
    PubMed
  • 5 Liu J, Lu L, Wood D, Lin S. ACS Cent. Sci. 2020; 6: 1317
    PubMed
  • 6 Prier CK, Rankic DA, MacMillan DWC. Chem. Rev. 2013; 113: 5322
    PubMed
  • 7 Shaw MH, Twilton J, MacMillan DWC. J. Org. Chem. 2016; 81: 6898
    PubMed
  • 8 Narayanam JMR, Stephenson CRJ. Chem. Soc. Rev. 2011; 40: 102
    PubMed
  • 9 Romero NA, Nicewicz DA. Chem. Rev. 2016; 116: 10075
    PubMed
  • 10 Schultz DM, Yoon TP. Science (Washington, D. C.) 2014; 343: 1239 176
  • 11 Science of Synthesis: Photocatalysis in Organic Synthesis. König B. Thieme; Stuttgart 2019
    Google Scholar
  • 12 Barham JP, König B. Angew. Chem. Int. Ed. 2020; 59: 11732
    PubMed
  • 13 Moutet J.-C, Reverdy G. J. Chem. Soc., Chem. Commun. 1982; 654
  • 14 Scheffold R, Orlinski R. J. Am. Chem. Soc. 1983; 105: 7200
  • 15 Romero NA, Margrey KA, Tay NE, Nicewicz DA. Science (Washington, D. C.) 2015; 349: 1326
    PubMed
  • 16 Morofuji T, Shimizu A, Yoshida J.-i. J. Am. Chem. Soc. 2013; 135: 5000
    PubMed
  • 17 Huang H, Strater ZM, Rauch M, Shee J, Sisto TJ, Nuckolls C, Lambert TH. Angew. Chem. Int. Ed. 2019; 58: 13318
    PubMed
  • 18 Wu S, Žurauskas J, Domański M, Hitzfeld PS, Butera V, Scott DJ, Rehbein J, Kumar A, Thyrhaug E, Hauer J, Barham JP. Org. Chem. Front. 2021; 8: 1132
  • 19 Liu Z, Zheng C, Xu X. CCS Chem. 2021; 3: 904 10.31635/ccschem.020.202000285
    Crossref
  • 20 Hou Z.-W, Xu H.-C. ChemElectroChem 2021; 8: 1571
  • 21 Huang H, Lambert TH. Angew. Chem. Int. Ed. 2021; 60: 11163
    PubMed
  • 22 Yan H, Song J, Zhu S, Xu H.-C. CCS Chem. 2021; 3: 317
  • 23 Huang H, Strater ZM, Lambert TH. J. Am. Chem. Soc. 2020; 142: 1698
    PubMed
  • 24 Huang H, Lambert TH. Angew. Chem. Int. Ed. 2020; 59: 658
    PubMed
  • 25 Yan H, Hou Z.-W, Xu H.-C. Angew. Chem. Int. Ed. 2019; 58: 4592
    PubMed
  • 26 Qiu Y, Scheremetjew A, Finger LH, Ackermann L. Chem.–Eur. J. 2020; 26: 3241
    PubMed
  • 27 Xu P, Chen P.-Y, Xu H.-C. Angew. Chem. Int. Ed. 2020; 59: 14275
    PubMed
  • 28 Capaldo L, Quadri LL, Merli D, Ravelli D. Chem. Commun. (Cambridge) 2021; 57: 4424
    PubMed
  • 29 Quattrini MC, Fujii S, Yamada K, Fukuyama T, Ravelli D, Fagnoni M, Ryu I. Chem. Commun. (Cambridge) 2017; 53: 2335
    PubMed
  • 30 Chen B, Wu L.-Z, Tung C.-H. Acc. Chem. Res. 2018; 51: 2512
    PubMed
  • 31 Lai X.-L, Shu X.-M, Song J, Xu H.-C. Angew. Chem. Int. Ed. 2020; 59: 10626
    PubMed
  • 32 Herold S, Bafaluy D, Muñiz K. Green Chem. 2018; 20: 3191
  • 33 Hu X, Zhang G, Bu F, Nie L, Lei A. ACS Catal. 2018; 8: 9370
  • 34 Shono T, Matsumura Y, Katoh S, Takeuchi K, Sasaki K, Kamada T, Shimizu R. J. Am. Chem. Soc. 1990; 112: 2368
  • 35 Wang F, Stahl SS. Angew. Chem. Int. Ed. 2019; 58: 6385
    PubMed
  • 36 Cibulka R, Vasold R, König B. Chem.–Eur. J. 2004; 10: 6223
  • 37 Zhang W, Carpenter KL, Lin S. Angew. Chem. Int. Ed. 2020; 59: 409
    PubMed
  • 38 Shen T, Lambert TH. Science (Washington, D. C.) 2021; 371: 620
    PubMed
  • 39 Shen T, Lambert TH. J. Am. Chem. Soc. 2021; 143: 8597
    PubMed
  • 40 Niu L, Jiang C, Liang Y, Liu D, Bu F, Shi R, Chen H, Chowdhury AD, Lei A. J. Am. Chem. Soc. 2020; 142: 17693
    PubMed
  • 41 Huang H, Lambert TH. J. Am. Chem. Soc. 2021; 143: 7247
    PubMed
  • 42 Kim H, Kim H, Lambert TH, Lin S. J. Am. Chem. Soc. 2020; 142: 2087
    PubMed
  • 43 Cowper NGW, Chernowsky CP, Williams OP, Wickens ZK. J. Am. Chem. Soc. 2020; 142: 2093
    PubMed
  • 44 Tian X, Karl TA, Reiter S, Yakubov S, de Vivie-Riedle R, König B, Barham JP. Angew. Chem. Int. Ed. 2021; 60: 20817
    PubMed