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• W1842205747 abstract "The radiofluorination of N-heterocyclic carbene (NHC) boron trifluoride adducts affords novel [(18)F]-positron emission tomography probes which resist hydrolytic fluoride release. The labelling protocol relies on an (18)F-(19)F isotopic exchange reaction promoted by the Lewis acid SnCl4. Modification of the NHC backbone with a maleimide functionality provides access to a model peptide conjugate which shows no evidence of defluorination when imaged in vivo." @default.
• W1842205747 created "2016-06-24" @default.
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• W1842205747 date "2015-01-01" @default.
• W1842205747 modified "2023-10-14" @default.
• W1842205747 title "[¹⁸F]–NHC–BF₃ adducts as water stable radio-prosthetic groups for PET imaging" @default.
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• W1842205747 doi "https://doi.org/10.1039/c5cc04545b" @default.
• W1842205747 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5457534" @default.
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• W1842205747 hasPublicationYear "2015" @default.
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