Deoxyfluorination is a primary method for the formation of C-F bonds. Bespoke reagents are commonly used because of issues associated with the low reactivity of metal fluorides. Reported here is the development of a simple strategy for deoxyfluorination, using first-row transition-metal fluorides, and it overcomes these limitations. Using CuF as an exemplar, activation of an O-alkylisourea adduct, formed in situ, allows effective nucleophilic fluoride transfer to a range of primary and secondary alcohols. Spectroscopic investigations have been used to probe the origin of the enhanced reactivity of CuF . The utility of the process in enabling F-radiolabeling is also presented.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.202001015 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!