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DOI: 10.1055/s-0040-1705951
Recent Advances in the Synthesis of Acyl Fluorides
We thank the Natural Sciences and Engineering Research Council of Canada (NSERC), the Fonds de recherche du Québec – Nature et technologies (FRQNT), OmegaChem, and the Université Laval.
Abstract
Acyl fluorides are valuable intermediates in organic synthesis. They are increasingly employed in peptide synthesis, in challenging esterification and amidation reactions or in transition-metal-catalyzed transformations. This review summarizes recent advances in their preparation.
1 Introduction
2 Nucleophilic Fluorination
2.1 α-Fluoroamine Reagents
2.2 Sulfur-Based Reagents
2.3 Metal Catalysts
2.4 Phosphorus-Based Reagents
2.5 N,N′-Dicyclohexylcarbodiimide/HF·Pyridine
2.6 Uranium Hexafluoride
2.7 Bromine Trifluoride
3 Radical Fluorination
4 Conclusion
Publication History
Received: 03 September 2020
Accepted: 28 September 2020
Article published online:
27 October 2020
© 2020. Thieme. All rights reserved
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