4.7 Article

Nucleophilic radiosynthesis of boron neutron capture therapy-oriented PET probe [18F]FBPA using aryldiboron precursors

期刊

CHEMICAL COMMUNICATIONS
卷 57, 期 71, 页码 8953-8956

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cc03369g

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  1. Ministry of Science and Technology, China [2016YFE0103600, 2017YFC0107700]

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A reliable copper-mediated nucleophilic radiosynthesis method was developed for preparing the PET imaging probe [F-18]FBPA using novel aryldiboron precursors. The carrier-free [F-18]FBPA with radiochemical purity >99% can be routinely prepared via a two-step synthesis with an automatic module and utilized for clinical PET imaging of tumours.
A reliable copper-mediated nucleophilic radiosynthesis of the PET imaging probe [F-18]FBPA was developed using novel aryldiboron precursors. The carrier-free [F-18]FBPA with radiochemical purity >99% was prepared routinely via the two-step synthesis with an automatic module and can be used for clinical PET imaging of tumours.

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