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DOI: 10.1055/a-2624-5212
Recent Update on Organic Electrochemical Reactions of Small-Molecule Alcohols
Supported by: The Lishui science & technology bureau, study on multifunctional composite coating for tunnels 2022GYX02
Funding Information We thank the Lishui Science and Technology Bureau for financial support under the project titled “Study on multifunctional composite coating for tunnels” (2022GYX02).

Abstract
Alcohols are among the most common organic reagents and are typically used as solvents. Small-molecule alcohols are inexpensive, water-soluble, easy to store, and stable in performance. Using alcohols as starting materials in organic electrochemical synthesis aligns with the principles of green chemistry. This review discusses organic electrochemical reactions involving small-molecule alcohols as reactants, mainly including etherification, esterification, and alkylation.
Publication History
Received: 22 April 2025
Accepted after revision: 29 May 2025
Accepted Manuscript online:
29 May 2025
Article published online:
31 July 2025
© 2025. Thieme. All rights reserved.
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References
- 1 Ali SK, Althikrallah HA, Alluhaibi MS. et al. Mol Catal 2024; 559: 114087
- 2 Budnikova YH, Dolengovski EL, Tarasov MV, Gryaznova TV. J Solid State Electrochem 2024; 28: 659
- 3a Novaes LFT, Liu J, Shen Y, Lu L, Meinhardt JM. Lin S Chem Soc Rev 2021; 50: 7941
- 3b Tian X, Liu Y, Yakubov S, Schütte J, Chiba S, Barham JP. Chem Soc Rev 2024; 53: 263
- 4 Liu J, Lu L, Wood D, Lin S. ACS Cent Sci 2020; 6: 1317
- 5a Villo P, Shatskiy A, Kärkäs MD, Lundberg H. Angew Chem Int Ed 2023; 62: e202211952
- 5b Qian H, Huang D, Bi Y, Yan G. Adv Synth Catal 2019; 361: 3240
- 6 Wala M, Simka W. Molecules 2021; 26: 2144
- 7 Wang T, Cao X, Jiao L. Angew Chem 2022; 134: e202213328
- 8 Christophe C, Baranton S. WIREs Energy Environ 2016; 5: 388
- 9 Wan J, Huang J. Org Lett 2022; 24: 8914
- 10 Wen L, Zhou N, Zhang Z. et al. Org Lett 2023; 25: 3308
- 11 Wang Y, Deng L, Mei H, Du B, Han J, Pan Y. Green Chem 2018; 20: 3444
- 12a Yang Z, Lu F, Li H. et al. Org Chem Front 2020; 7: 4064
- 12b Zhang H, Xiong Y, Luo M. et al. Org Chem Front 2023; 10: 3786
- 13a Liu C, Shen Y, Xiao Z. et al. Green Chem 2019; 21: 4030
- 13b Huang R, Yu C, Patureau F W. Chem Electro Chem 2021; 8: 3943
- 13c Braun M, Andronescu C. Chem Cat Chem 2025; 17: e202402013
- 14 Jiang X, Yang L, Ye L. et al. Eur J Org Chem 2020; 11: 1687
- 15 Bu F, Lu L, Hu X, Wang S, Zhang H, Lei A. Chem Sci 2020; 36: 10000
- 16 Liu H, Li L, Wang G. et al. Adv Synth Catal 2023; 365: 3586
- 17 Wang D, Jiang T, Wan H. et al. Angew Chem Int Ed 2022; 61: e202201543
- 18 Qin H, Yang Z, Zhang Z. et al. Chem Eur J 2021; 27: 13024
- 19 Hu Y, Liu X, Feng C, Wang J, Li M, Shen Z. Adv Synth Catal 2020; 2024: 366
- 20 Han J, Haines C, Piane J, Filien L, Nacsa E. J Am Chem Soc 2023; 145: 15680
- 21 Yu C, Özkaya B, Patureau FW. Chem Eur J 2021; 27: 3682
- 22 Zhong Q, Wang PL, Gao H, Liu F, Li H. J Org Chem 2024; 18: 13253
- 23 Yamamoto K, Kuriyama M, Onomura O. Isr J Chem 2024; 64: e202300068
- 24 Hilt G. ChemElectroChem 2020; 7: 395