Cobalt-Catalyzed Alkene Alkylarylation: Access to Pyrrolidinones
Practical cyclization and cross-coupling reactions between alkenyl-substituted alkyl bromides and arylzinc pivalates via cobalt-catalyzed sequential C(sp<sup>3</sup>)-C(sp<sup>3</sup>)/C(sp<sup>3</sup>)-C(sp<sup>2</sup>) bond formation have been disclosed, thus providing straightforward access to structurally diverse pyrrolidinones. Moreover, this approach could be also effective for the modular preparation of spirocyclic pyrrolidinones through spirocyclized alkene alkylarylation. Beyond that, rather mild conditions, synthetic simplicity, and excellent functional group compatibility show the potential applications of this method in synthetic chemistry.
Authors
- Jie Li (ORCID: https://orcid.org/0000-0002-6912-3346)
- Chenhao Huang (ORCID: https://orcid.org/0000-0001-8544-9103)
- Changrui Nie
- Qian Zhang (ORCID: https://orcid.org/0000-0002-8793-0520)
- Kaixin Chen (ORCID: https://orcid.org/0000-0002-1987-3800)
- Junda Wang
Institutions
- University of Liverpool (GB)
- Soochow University (CN)
- Laboratoire de Synthèse Organique (FR)
- Materials Research Center (IN)
- Xi’an Jiaotong-Liverpool University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-08-12
- DOI
- https://doi.org/10.1021/acs.orglett.5c02870
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Jiangsu Province