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A Convenient Synthesis of Difluoroalkyl Ethers from Thionoesters Using Silver(I) Fluoride.
Newton, Josiah; Driedger, Daniel; Nodwell, Matthew B; Schaffer, Paul; Martin, Rainer E; Britton, Robert; Friesen, Chadron M.
Afiliação
  • Newton J; Department of Chemistry, Simon Fraser University, Burnaby, British Columbia, V5A 1S6, Canada.
  • Driedger D; Department of Chemistry, Trinity Western University, Langley, British Columbia, V2Y 1Y1, Canada.
  • Nodwell MB; Department of Chemistry, Trinity Western University, Langley, British Columbia, V2Y 1Y1, Canada.
  • Schaffer P; Department of Chemistry, Simon Fraser University, Burnaby, British Columbia, V5A 1S6, Canada.
  • Martin RE; Life Sciences Division, TRIUMF, Vancouver, British Columbia, V6T 2A3, Canada.
  • Britton R; Medicinal Chemistry, Roche Pharma Research and Early Development (pRED), Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, 4070, Basel, Switzerland.
  • Friesen CM; Department of Chemistry, Simon Fraser University, Burnaby, British Columbia, V5A 1S6, Canada.
Chemistry ; 25(70): 15993-15997, 2019 Dec 13.
Article em En | MEDLINE | ID: mdl-31538366
ABSTRACT
Herein we report the mild and rapid fluorodesulfurization of thionoesters using only silver(I) fluoride. This reaction demonstrates excellent functional group tolerance and complements existing strategies for difluoroalkyl ether synthesis, which rely on toxic and often dangerous reagents that demonstrate limited functional group compatibility. We additionally report the translation of this finding to the production of 18 F-labelled difluoroalkyl ethers using fluoride-derived [18 F]AgF. This new process should enable the synthesis of a wide range of difluoroalkyl ethers with applications in medicinal and materials chemistry, and radiotracer production.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article