Palladium-Catalyzed α-Arylation of Nitroalkanes with Aryl Fluorosulfonates for Convenient Access to α-Arylated Nitroalkanes

Palladium-catalyzed α-arylation of nitroalkanes by utilizing aryl fluorosulfonates as effective arylating agents can be realized. The reactions proceed effectively through C-O bond activation to produce a variety of valuable α-arylated nitroalkanes in modest to good yields with wide functional group compatibility. Additionally, late-stage functionalization of complex molecules and scale-up synthesis can be achieved.

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Journal
The Journal of Organic Chemistry
Published
2025-08-14
DOI
https://doi.org/10.1021/acs.joc.5c01502
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Palladium-Catalyzed α-Arylation of Nitroalkanes with Aryl Fluorosulfonates for Convenient Access to α-Arylated Nitroalkanes

Chenlong Zhu, Fei Zhao, Weidong Rao, Xue‐Qiang Chu et al.
The Journal of Organic Chemistry
Catalytic Cross-Coupling Reactions
article

Palladium-Catalyzed α-Arylation of Nitroalkanes with Aryl Fluorosulfonates for Convenient Access to α-Arylated Nitroalkanes

Chenlong Zhu, Fei Zhao, Weidong Rao, Xue‐Qiang Chu, Zhi‐Liang Shen, Hao Xu, Yuanyuan Wang, Chengping Miao
article en

Abstract

Palladium-catalyzed α-arylation of nitroalkanes by utilizing aryl fluorosulfonates as effective arylating agents can be realized. The reactions proceed effectively through C-O bond activation to produce a variety of valuable α-arylated nitroalkanes in modest to good yields with wide functional group compatibility. Additionally, late-stage functionalization of complex molecules and scale-up synthesis can be achieved.

The Journal of Organic ChemistryVol. 90(34)
Nanjing Tech University (CN), Nanjing Forestry University (CN), Jiaxing University (CN), Institute of Chemical Industry of Forest Products (CN), Fluorochem (United States) (US)
Nanjing Tech University
Openalex Percentile: Top 85%
Catalytic Cross-Coupling Reactions
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