Organometallic Reagent-Free Iron-Catalyzed C–Cl Bond Activation of Aryl Chlorines

The formation of C-C and C-S bonds is fundamentally important for the production of pharmaceuticals, biologically active molecules, and organic natural products. Herein, we report an unprecedented iron-catalyzed process for C-C and C-S bond coupling to achieve the 1,2-arylthiolation of alkenes. This process proceeds efficiently without the use of organometallic reagents and features readily available starting materials, a broad substrate scope, and simple reaction conditions.

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Publication Details

Journal
Organic Letters
Published
2025-04-01
DOI
https://doi.org/10.1021/acs.orglett.5c00877
Citations
2
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
1.87

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article

Organometallic Reagent-Free Iron-Catalyzed C–Cl Bond Activation of Aryl Chlorines

Dayong Shi, Leifeng Yuan, Cong Shi, Xiangqian Li et al.
2 citations
Organic Letters
Catalytic Cross-Coupling Reactions
1.87
article

Organometallic Reagent-Free Iron-Catalyzed C–Cl Bond Activation of Aryl Chlorines

Dayong Shi, Leifeng Yuan, Cong Shi, Xiangqian Li, Zemin Wang, Xiaowei Li, Wenli Zhuang
article en
2 citations

Abstract

The formation of C-C and C-S bonds is fundamentally important for the production of pharmaceuticals, biologically active molecules, and organic natural products. Herein, we report an unprecedented iron-catalyzed process for C-C and C-S bond coupling to achieve the 1,2-arylthiolation of alkenes. This process proceeds efficiently without the use of organometallic reagents and features readily available starting materials, a broad substrate scope, and simple reaction conditions.

Organic LettersVol. 27(14)
Shandong University (CN), Qingdao Binhai University (CN), Qingdao National Laboratory for Marine Science and Technology (CN)
Department of Science and Technology of Shandong Province, Natural Science Foundation of Shandong Province, Key Technology Research and Development Program of Shandong, National Key Research and Development Program of China
Openalex Percentile: Top 17%
Catalytic Cross-Coupling Reactions
1.87
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