Copper(I)-Mediated 11C-Carboxylation of (Hetero)arylstannanes
Author(s) -
Ian R. Duffy,
Neil Vasdev,
Kenneth Dahl
Publication year - 2020
Publication title -
acs omega
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.0c00524
Subject(s) - carboxylation , radiosynthesis , chemistry , yield (engineering) , medicinal chemistry , stoichiometry , copper , carbon dioxide , nuclear chemistry , radiochemistry , organic chemistry , catalysis , in vivo , materials science , microbiology and biotechnology , metallurgy , biology
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 [ 11 C]CO 2 . The methodology was applied to the radiosynthesis of the retinoid X receptor agonist, [ 11 C]bexarotene, with a decay-corrected radiochemical yield of 32 ± 5% and molar activity of 38 ± 23 GBq/μmol ( n = 3).
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