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Radiosynthesis of the anticancer nucleoside analogue Trifluridine using an automated (18)F-trifluoromethylation procedure
Trifluoromethyl groups are widespread in medicinal chemistry, yet there are limited (18)F-radiochemistry techniques available for the production of the complementary PET agents. Herein, we report the first radiosynthesis of the anticancer nucleoside analogue trifluridine, using a fully automated, cl...
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| Publicado no: | Org Biomol Chem |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Royal Society of Chemistry
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5944245/ https://ncbi.nlm.nih.gov/pubmed/29629716 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c8ob00432c |
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