eFluorination of activated alcohols using collidinium tetrafluoroborate

Article


Kiaku, C., Martinage, D., Sicim, Y., Leech, M.C., Walsh, J.M., Poole, D.L., Mason, J., Goodall, I.C.A., Devo, P. and Lam, K. 2023. eFluorination of activated alcohols using collidinium tetrafluoroborate. Organic Letters. 26 (14), pp. 2697-2701. https://doi.org/10.1021/acs.orglett.3c00976
TypeArticle
TitleeFluorination of activated alcohols using collidinium tetrafluoroborate
AuthorsKiaku, C., Martinage, D., Sicim, Y., Leech, M.C., Walsh, J.M., Poole, D.L., Mason, J., Goodall, I.C.A., Devo, P. and Lam, K.
Abstract

Tertiary C–F bonds are important structural designs; however, they suffer from challenging synthesis. Current methodologies use corrosive amine-HF salts or expensive and hazardous catalysts and reagents. Our group recently introduced collidinium tetrafluoroborate as an efficient fluorinating agent for anodic decarboxyfluorination reactions. Nevertheless, tertiary carboxylic acids are less readily available and more challenging to prepare than their alcohol analogues. Herein we report a practical, mild, and cheap electrochemical method to achieve deoxyfluorination of hindered carbon centers.

Sustainable Development Goals12 Responsible consumption and production
Middlesex University ThemeSustainability
PublisherAmerican Chemical Society (ACS)
JournalOrganic Letters
ISSN1523-7060
Electronic1523-7052
Publication dates
Online19 May 2023
Print12 Apr 2024
Publication process dates
Submitted26 Mar 2023
Deposited02 Jun 2025
Output statusPublished
Digital Object Identifier (DOI)https://doi.org/10.1021/acs.orglett.3c00976
Web of Science identifierWOS:001012080200001
Related Output
Has versionhttps://gala.gre.ac.uk/id/eprint/42709/
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