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Sulfinamide Crossover Reaction.

Vladimír NosekJiří Míšek
Published in: The Journal of organic chemistry (2024)
This study unveils a new catalytic crossover reaction of sulfinamides. Leveraging mild acid catalysis, the reaction demonstrates a high tolerance to structural variations, yielding equimolar products across diverse sulfinamide substrates. Notably, small sulfinamide libraries can be selectively oxidized to sulfonamides, providing a new platform for ligand optimization and discovery in medicinal chemistry. This crossover chemotype provides a new tool for high-throughput experimentation in discovery chemistry.
Keyphrases
  • high throughput
  • open label
  • double blind
  • placebo controlled
  • small molecule
  • single cell
  • drug discovery
  • clinical trial
  • randomized controlled trial
  • mass spectrometry
  • visible light
  • simultaneous determination