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.

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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

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article

Cobalt-Catalyzed Alkene Alkylarylation: Access to Pyrrolidinones

Jie Li, Chenhao Huang, Changrui Nie, Qian Zhang et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Cobalt-Catalyzed Alkene Alkylarylation: Access to Pyrrolidinones

Jie Li, Chenhao Huang, Changrui Nie, Qian Zhang, Kaixin Chen, Junda Wang
article en

Abstract

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.

Organic LettersVol. 27(33)
University of Liverpool (GB), Soochow University (CN), Laboratoire de Synthèse Organique (FR), Materials Research Center (IN), Xi’an Jiaotong-Liverpool University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province
Clean water and sanitation
Openalex Percentile: Top 85%
Catalytic C–H Functionalization Methods
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