Highly selective electrochemical fluorination of dithioacetal derivatives bearing electron-withdrawing substituents at the position α to the sulfur atom using poly(HF) salts

Scholarly Works

• Gombos, L. G.; Nikl, J.; Waldvogel, S. R. Dual Roles of Supporting Electrolytes in Organic Electrosynthesis. ChemElectroChem 2024, 11. doi:10.1002/celc.202300730
• Bhamare, V. S.; Kulkarni, R. M. An evolution in electrochemical and chemical synthesis applications in prospects of ionic liquids. Advanced Applications of Ionic Liquids; Elsevier, 2023; pp 113–154. doi:10.1016/b978-0-323-99921-2.00011-2
• Fuchigami, T.; Inagi, S. doi:10.1002/9780470682531.pat1010
• Yin, B.; Inagi, S.; Fuchigami, T. Selective electrochemical fluorination of O,S‐acetal derivatives bearing α‐electron‐withdrawing groups. Electrochemical Science Advances 2021, 2. doi:10.1002/elsa.202100181
• Thadathil, D. A.; Varghese, A.; Radhakrishnan, K. V. Review—Electrochemical Strategies for Selective Fluorination of Organic Compounds. Journal of The Electrochemical Society 2021, 168, 075503. doi:10.1149/1945-7111/ac148f
• Ito, S.; Kondo, K.; Ishii, H.; Inagi, S.; Fuchigami, T. Electrochemical Fluorination of (Arylthio)methyl Carboxylates and γ-Phenylthio-γ-butyrolactone Derivative. Journal of The Electrochemical Society 2021, 168, 065502. doi:10.1149/1945-7111/ac07c2
• Scheide, M. R.; Nicoleti, C. R.; Martins, G. M.; Braga, A. L. Electrohalogenation of organic compounds. Organic & biomolecular chemistry 2021, 19, 2578–2602. doi:10.1039/d0ob02459g
• Smeyne, D.; Verboom, K.; Bryan, M.; Lobue, J. M.; Shaikh, A. Electrochemical esterification via oxidative coupling of aldehydes and alcohols. Tetrahedron Letters 2021, 68, 152898. doi:10.1016/j.tetlet.2021.152898
• Haufe, G. Et3N·3HF Complex Fluorination for Preparing Alkyl Fluorides. Fluorination; Springer Singapore, 2020; pp 137–181. doi:10.1007/978-981-10-3896-9_26
• Yakubov, S.; Barham, J. P. Photosensitized direct C-H fluorination and trifluoromethylation in organic synthesis. Beilstein journal of organic chemistry 2020, 16, 2151–2192. doi:10.3762/bjoc.16.183
• Fuchigami, T.; Inagi, S. Recent Advances in Electrochemical Systems for Selective Fluorination of Organic Compounds. Accounts of chemical research 2020, 53, 322–334. doi:10.1021/acs.accounts.9b00520
• Spurlin, S.; Blocker, M.; Lobue, J. M.; Wu, J.; Padgett, C. W.; Shaikh, A. Regioselective Electrolytic 5,8-Difluorination of Quinolines. Tetrahedron Letters 2020, 61, 151474. doi:10.1016/j.tetlet.2019.151474
• Francke, R.; Gonzalez, L.; Little, R. D.; Moeller, K. D. Surface and Interface Science; Wiley, 2020; pp 827–891. doi:10.1002/9783527822508.ch79
• Oyanagi, S.; Ishii, H.; Inagi, S.; Fuchigami, T. Electrochemical Properties and Fluorination of Cyclopropane Derivatives Bearing Arylthio Groups. Journal of The Electrochemical Society 2020, 167, 155511. doi:10.1149/1945-7111/abb83b
• Haufe, G. Et 3 N·3HF Complex Fluorination for Preparing Alkyl Fluorides. Fluorination; Springer Singapore, 2018; pp 1–44. doi:10.1007/978-981-10-1855-8_26-1
• Sen, L.; Xu, K.; Zeng, C.-C.; Tian, H.; Sun, B. Recent Advances in the Electrochemical α‐C–H Bond Functionalization of Carbonyl Compounds. Advanced Synthesis & Catalysis 2018, 360, 4266–4292. doi:10.1002/adsc.201800519
• Kärkäs, M. D. Electrochemical strategies for C-H functionalization and C-N bond formation. Chemical Society reviews 2018, 47, 5786–5865. doi:10.1039/c7cs00619e
• Lopez-Lopez, E. E.; Pérez-Bautista, J. A.; Sartillo-Piscil, F.; Frontana-Uribe, B. A. Electrochemical Corey-Winter reaction. Reduction of thiocarbonates in aqueous methanol media and application to the synthesis of a naturally occurring α-pyrone. Beilstein journal of organic chemistry 2018, 14, 547–552. doi:10.3762/bjoc.14.41
• Lennox, A. J. J.; Nutting, J. E.; Stahl, S. S. Selective electrochemical generation of benzylic radicals enabled by ferrocene-based electron-transfer mediators. Chemical science 2017, 9, 356–361. doi:10.1039/c7sc04032f
• Xu, L.; Wang, H.; Zheng, C.; Zhao, G. One-pot synthesis of (ethoxycarbonyl)difluoromethylthioethers from thiocyanate sodium and ethyl 2-(trimethylsilyl)-2,2-difluoroacetate (TMS-CF2CO2Et). Tetrahedron 2017, 73, 6057–6066. doi:10.1016/j.tet.2017.08.048

Explore citations to this article at