AI Article Synopsis

  • Allyl sulfones are important components in many active pharmaceutical compounds, but their synthesis can be challenging due to existing barriers.* -
  • The authors present an effective method using organophotocatalysis, allowing for the creation of various allyl sulfone derivatives using affordable sodium sulfinate salts under mild conditions, achieving good yields and high selectivity.* -
  • This study also showcases the adaptability of the method for larger-scale synthesis and further functionalization of allyl sulfones, with a proposed mechanism for the sulfonylation process explained through control experiments.*

Article Abstract

Allyl sulfones are an essential pharmacophore in many bioactive compounds. To combat their synthetic barrier, we report a practical, straightforward organophotocatalyzed methodology for accessing miscellaneously functionalized allyl sulfone derivatives using inexpensive and bench-stable sodium sulfinate salts under mild conditions. This photo-catalyzed radical sulfonylation provides access to a variety of allyl sulfones in good to excellent yields with high E : Z selectivity. A wide range of vinyl cyclopropanes, as well as aryl/hetero and alkyl sodium sulfinates, were tolerated and reliable in gram-scale synthesis. Later on, further functionalization of allyl sulfones was demonstrated. A plausible mechanism for radical sulfonylation is proposed from the control experiments.

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Source
http://dx.doi.org/10.1002/chem.202303187DOI Listing

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