Palladium nanoparticles for aerobic oxidative Heck arylation of alkenes
Abstract Herein, we report a palladium nanoparticle-catalyzed aerobic oxidative Heck arylation of alkenes with aryl boronic acids, yielding a range of (E)-β-aryl acrylates and (E)-stilbene derivatives. This reaction uses molecular oxygen as the terminal oxidant, requiring no base or additional oxidants. The catalyst displays notable tolerance to unprotected amide groups, surpassing conventional strategies.
Authors
- Yasushi Obora (ORCID: https://orcid.org/0000-0003-3702-9969)
- Kazuki Tabaru (ORCID: https://orcid.org/0000-0001-5587-5670)
- Takeyuki Suzuki (ORCID: https://orcid.org/0000-0002-2137-0276)
- Haruka Nishimura
Institutions
- Kansai University (JP)
Publication Details
- Journal
- Chemistry Letters
- Published
- 2025-03-27
- DOI
- https://doi.org/10.1093/chemle/upaf068
- Citations
- 2
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.87