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Carbon-11 carboxylation of trialkoxysilane and trimethylsilane derivatives using [11C]CO2.


ABSTRACT: A novel carboxylation radiosynthesis methodology is described starting from cyclotron-produced [11C]CO2 and fluoride-activated silane derivatives. Six carbon-11 labelled carboxylic acids were obtained from their corresponding trimethylsilyl and trialkoxysilyl precursors in a one-pot labelling methodology. The radiochemical yields ranged from 19% to 93% within 12 minutes post [11C]CO2 delivery with a trapping efficiency of 21-89%.

SUBMITTER: Bongarzone S 

PROVIDER: S-EPMC7384297 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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Carbon-11 carboxylation of trialkoxysilane and trimethylsilane derivatives using [<sup>11</sup>C]CO<sub>2</sub>.

Bongarzone Salvatore S   Raucci Nicola N   Fontana Igor Camargo IC   Luzi Federico F   Gee Antony D AD  

Chemical communications (Cambridge, England) 20200325 34


A novel carboxylation radiosynthesis methodology is described starting from cyclotron-produced [<sup>11</sup>C]CO<sub>2</sub> and fluoride-activated silane derivatives. Six carbon-11 labelled carboxylic acids were obtained from their corresponding trimethylsilyl and trialkoxysilyl precursors in a one-pot labelling methodology. The radiochemical yields ranged from 19% to 93% within 12 minutes post [<sup>11</sup>C]CO<sub>2</sub> delivery with a trapping efficiency of 21-89%. ...[more]

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