Methylative Cyclization of α-Substituted Styrenes Mediated by Excited Dibenzothiophene S-Oxide
Radical-mediated carbofunctionalization of olefins with alkyl radicals has been extensively studied as a powerful tool for skeletal construction in organic synthesis. However, methyl-functionalization reactions to introduce the smallest carbon substituent remain relatively unexplored because methods for generating methyl radicals are limited.In this study, we found that excited dibenzothiophene S-oxide promotes methyl radical generation from DMSO, enabling methylative cyclization of olefins to afford a variety of heterocycles. This transformation proceeds under mild conditions using an excited sulfoxide as the oxidant without relying on explosive peroxides.
Authors
- Hideki Yorimitsu (ORCID: https://orcid.org/0000-0002-0153-1888)
- Saki Maejima (ORCID: https://orcid.org/0009-0002-8043-1064)
- Yuto Tamba
- Toshisato Egashira
Institutions
- Kyoto University (JP)
Publication Details
- Journal
- Synthesis
- Published
- 2026-07-24
- DOI
- https://doi.org/10.1055/a-2921-1171
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00