Selective Synthesis of Monofluorinated Compounds Applying Amine/HF Reagents

Abstract

AbstractFor nucleophilic monofluorination, amine/HF reagents such as Et3N⋅3HF, Pyr⋅9HF (Olah's reagent) and similar combinations belong to the most frequently used fluoride sources, whereupon the selectivity of these reagents can be very different depending of its acidity, the nucleophilicity of the fluoride equivalent, and the structure of the particular substrate. These reagents can be used safely in ordinary chemistry laboratories for nucleophilic substitution reactions by fluoride at sp3‐hybridized carbon centers. For ring opening reactions of epoxides, the regio‐ and stereoselectivity is very much depending of the nature of the epoxide and the acidity of the HF reagent favoring either SN1 or SN2 type reactions. Similarly, the outcome of halofluorination and similar reactions with sulfur or seleno electrophiles can be controlled by the particular combination of the electrophile and the fluoride source. Examples for the application of these reaction types for the synthesis of fluorine‐containing analogues of natural products or biologically relevant compounds are in the focus of this personal account.