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March 10, 2026European Journal of Inorganic Chemistry0 citations

Double Functionalization of Atropisomeric Biphenyl Sulfoxides by Ortho ‐Metalation and DYKAT Toward Chiral Quaterphenyl‐Based Borane Lewis Acids

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JBJordan BerreurJBJulien BortoluzziLKLaura Köring

Key Points

  • The research aims to develop new chiral backbones for Lewis acids through functionalization of biphenyl sulfoxides.
  • Utilized ortho-metalation techniques on stereopure biphenyl tosyl sulfoxides.
  • Employed dynamic kinetic asymmetric arylative cross-coupling to create unique chiral compounds.
  • Converted sulfinyl groups to boron-based structures for chiral Lewis acid applications.
  • Successfully synthesized chiral quaterphenyl tolyl sulfoxides from biphenyl sulfoxides.
  • Achieved efficient transformation of sulfinyl groups into boron-based Lewis acids.
  • Demonstrated the potential utility of chiral boron-based acids in enantioselective catalysis.

Abstract

In the young field of enantioselective catalysis by frustrated Lewis pairs, the search for new chiral backbones for Lewis acids is desirable for future developments of the field. By taking advantage of the toluenesulfinyl group, a very useful traceless chiral auxiliary, it was possible to decorate stereopure axially chiral biphenyl tolyl sulfoxides and access unique chiral quaterphenyl tolyl sulfoxides by directed ortho ‐metalation and electrophile trapping as well as a dynamic kinetic asymmetric arylative cross‐coupling. The resulting chiral backbone is amenable to accessing chiral boron‐based Lewis acids by conversion of the sulfinyl group to boron‐based ones.

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Cite This Study

Berreur et al. (2026) studied this question.

synapsesocial.com/papers/69af951a70916d39fea4c498https://doi.org/10.1002/ejic.70158
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