The first radiosynthesis of 2-amino-5-[18F]fluoropyridines via a “minimalist” radiofluorination/palladium-catalyzed amination sequence from anisyl(2-bromopyridinyl)iodonium triflate

Mathilde Pauton; Raphaël Gillet; Catherine Aubert; Guillaume Bluet; Florence Gruss-Leleu; Sébastien Roy; Cécile Perrio

doi:10.1039/C9OB01187K

Journal articles

The first radiosynthesis of 2-amino-5-[18F]fluoropyridines via a “minimalist” radiofluorination/palladium-catalyzed amination sequence from anisyl(2-bromopyridinyl)iodonium triflate

Mathilde Pauton ^{1, 2} Raphaël Gillet ¹ Catherine Aubert ² Guillaume Bluet ² Florence Gruss-Leleu ² Sébastien Roy ² Cécile Perrio ¹

1 ISTCT - Imagerie et Stratégies Thérapeutiques des pathologies Cérébrales et Tumorales

2 Sanofi [Vitry-sur-Seine]

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Journal articles

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Chemical Sciences

Chemical Sciences / Radiochemistry

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https://hal-normandie-univ.archives-ouvertes.fr/hal-02155028
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Submitted on : Thursday, June 13, 2019 - 12:08:01 PM
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The first radiosynthesis of 2-amino-5-[18F]fluoropyridines via a “minimalist” radiofluorination/palladium-catalyzed amination sequence from anisyl(2-bromopyridinyl)iodonium triflate

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The first radiosynthesis of 2-amino-5-[18F]fluoropyridines via a “minimalist” radiofluorination/palladium-catalyzed amination sequence from anisyl(2-bromopyridinyl)iodonium triflate

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