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| Hauptseite > Publikationsdatenbank > Minimalist approach meets green chemistry: Synthesis of 18F-labeled (hetero)aromatics in pure ethanol > print |
| Hauptseite > Publikationsdatenbank > Minimalist approach meets green chemistry: Synthesis of 18F-labeled (hetero)aromatics in pure ethanol > print |
| 001 | 863802 | ||
| 005 | 20210130002324.0 | ||
| 024 | 7 | _ | |a 10.1002/jlcr.3776 |2 doi |
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| 100 | 1 | _ | |a Zlatopolskiy, Boris D. |0 P:(DE-Juel1)176188 |b 0 |u fzj |
| 245 | _ | _ | |a Minimalist approach meets green chemistry: Synthesis of 18F-labeled (hetero)aromatics in pure ethanol |
| 260 | _ | _ | |a New York, NY [u.a.] |c 2019 |b Wiley |
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| 520 | _ | _ | |a The application of toxic solvents and additives is inevitable for most of the described protocols for 18F‐labeling. Herein, a novel “green” procedure for nucleophilic aromatic radiofluorination of highly activated (hetero)aromatic substrates in pure EtOH is described. Using this method a series of 18F‐labeled (hetero)arenes have been synthesized in radiochemical yields (RCYs) of up to 97%. |
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| 700 | 1 | _ | |a Neumaier, Bernd |0 P:(DE-Juel1)166419 |b 5 |e Corresponding author |
| 773 | _ | _ | |a 10.1002/jlcr.3776 |g Vol. 62, no. 8, p. 404 - 410 |0 PERI:(DE-600)1491841-9 |n 8 |p 404 - 410 |t Journal of labelled compounds and radiopharmaceuticals |v 62 |y 2019 |x 0362-4803 |
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