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- W4306762007 abstract "Radiolabeled amino acids are an important class of agents for positron emission tomography imaging that target amino acid transporters in many tumor types. Traditional 18F-labeled amino acid synthesis strategies are always based on nucleophilic aromatic substitution reactions with multistep radiosynthesis and low radiochemical yields. In recent years, new 18F-labeling methodologies such as metal-catalyzed radiofluorination and heteroatom (B, P, S, Si, etc.)-18F bond formation are being effectively used to synthesize radiopharmaceuticals. This review focuses on recent advances in the synthesis, radiolabeling, and application of a series of 18F-labeled amino acid analogs using new 18F-labeling strategies." @default.
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- W4306762007 date "2022-10-17" @default.
- W4306762007 modified "2023-10-14" @default.
- W4306762007 title "Recent Advances in 18F-Labeled Amino Acids Synthesis and Application" @default.
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- W4306762007 doi "https://doi.org/10.3390/pharmaceutics14102207" @default.
- W4306762007 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36297641" @default.
- W4306762007 hasPublicationYear "2022" @default.
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