Copper(I)-Mediated 11C-Carboxylation of (Hetero)arylstannanes

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Abstract

A novel copper-mediated carboxylation strategy of aryl- and heteroaryl-stannanes is described. The method serves as a mild (i.e., 1 atm) carboxylation method using stable carbon dioxide and is transferable as a radiosynthetic approach for carbon-11-labeled aromatic and heteroaromatic carboxylic acids using sub-stoichiometric quantities of [11C]CO2. The methodology was applied to the radiosynthesis of the retinoid X receptor agonist, [11C]bexarotene, with a decay-corrected radiochemical yield of 32 ± 5% and molar activity of 38 ± 23 GBq/μmol (n = 3).

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Duffy, I. R., Vasdev, N., & Dahl, K. (2020). Copper(I)-Mediated 11C-Carboxylation of (Hetero)arylstannanes. ACS Omega, 5(14), 8242–8250. https://doi.org/10.1021/acsomega.0c00524

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