S <sub>H</sub> 2 Decarboxylative Monofluoromethylation of Aliphatic Carboxylic Acids Enabled by Nickel/Photoredox Dual Catalysis
Abstract
Abstract Catalytic construction of alkyl fluorides through C─C bond‐forming transformations represents a formidable challenge in modern organofluorine chemistry. In this work, we present a decarboxylative monofluoromethylation protocol enabled by synergistic nickel/photoredox dual catalysis for aliphatic carboxylic acid derivatives. A structurally diverse array of tertiary, secondary, and primary N ‐hydroxyphthalimide (NHP) esters underwent efficient conversion to their corresponding fluoromethylated products with excellent functional group tolerance (68 examples, up to 91% yield). The methodology's versatility was highlighted through late‐stage monofluoromethylation of pharmaceutically relevant molecules. Mechanistic investigations reveal the involvement of a radical rebound pathway mediated by nickel (III) intermediate, with the homolytic substitution (S H 2) process at sterically congested center representing a critical mechanistic distinction from conventional cross‐coupling paradigms.
Article Details
Authors (5)
Ting‐Yu Fang
Department of Chemistry State Key Laboratory of Synthetic Biology Tianjin University Tianjin 300072 P.R. China
Meng‐Ye Jiang
Department of Chemistry State Key Laboratory of Synthetic Biology Tianjin University Tianjin 300072 P.R. China
Meng‐Meng Zheng
State Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences Shanghai 200032 P.R. China
Jun‐An Ma
Department of Chemistry State Key Laboratory of Synthetic Biology Frontiers Science Center For Synthetic Biology (Ministry of Education) Tianjin University Tianjin P. R. China
Fa‐Guang Zhang
Department of Chemistry State Key Laboratory of Synthetic Biology Frontiers Science Center For Synthetic Biology (Ministry of Education) Tianjin University Tianjin P. R. China