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Updated: Jan 18, 2026

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Strategic advances in C-OCF3 bond transformations.
Zhenbang Chang1, Arushi Garg1, Tatiana Besset1
1INSA Rouen Normandie, Univ Rouen Normandie, Univ Caen Normandie, ENSICAEN, CNRS, Institut CARMeN (UMR 6064), F-76000 Rouen, France. tatiana.besset@insa-rouen.fr.
Cleaving the aryl C-OCF3 bond is challenging but advances enable new C-C, C-H, and C-heteroatom bond formations. This review highlights progress in activating this strong bond for synthetic chemistry.
Area of Science:
- Organic Chemistry
- Synthetic Chemistry
Background:
- Trifluoromethoxylated arenes are important synthetic targets.
- The cleavage of the aryl C-OCF3 bond is synthetically challenging.
- Few methods exist for the selective activation of the C-OCF3 group.
Purpose of the Study:
- To review recent advances in the activation of the aryl C-OCF3 bond.
- To highlight methods enabling C-C, C-H, and C-heteroatom bond formations.
- To underscore the potential of this emerging field in synthetic chemistry.
Main Methods:
- Review of literature on C-OCF3 bond activation.
- Analysis of key synthetic transformations.
- Categorization of bond formation strategies.
Main Results:
- Significant progress has been made in activating the strong aryl C-OCF3 bond.
- Novel methodologies enable the formation of new carbon-carbon bonds.
- Methods for C-H and C-heteroatom bond formation have been developed.
Conclusions:
- The activation of the aryl C-OCF3 bond is a rapidly developing area.
- These advances offer new synthetic routes and possibilities.
- Further research holds transformative potential for organic synthesis.
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