Abstract
Herein we report the deoxygenated fluorination of readily available carboxylic acids. A series of acyl fluorides have been synthesized using shelf-stable N-trifluoromethylthiophthalimide as a fluorinated reagent for the first time. Scale-up reactions and sequential cross-couplings were performed successfully to demonstrate the practicability of this fluorination protocol.
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CITATION STYLE
APA
Zhu, C., Zhumagazy, S., Yue, H., & Rueping, M. (2022). Electrophilic: N -trifluoromethylthiophthalimide as a fluorinated reagent in the synthesis of acyl fluorides. Organic Chemistry Frontiers, 9(2), 342–346. https://doi.org/10.1039/d1qo01633d
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