Related Experiment Video
Updated: Apr 1, 2026

A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species
Published on: August 16, 2018
Copper-Catalyzed Enantioconvergent Nucleophilic Fluorination of Alkyl Electrophiles to Generate α-Fluoroamides
1Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States of America.
Abstract:
Despite the pharmaceutical significance of alkyl fluorides wherein a fluorine-bearing carbon is stereogenic, progress in the development of catalytic asymmetric methods for their synthesis has been limited; furthermore, the approaches that have been described to date predominantly employ electrophilic fluorinating agents (e.g., NFSI and Selectfluor) rather than more economical nucleophilic fluorinating agents (e.g., CsF and KF). Herein, we describe a method for the catalytic asymmetric synthesis of alkyl fluorides through copper-catalyzed enantioconvergent substitutions of racemic alkyl halides, specifically, fluorinations of α-haloamides by CsF, enabling carbon-fluorine bond formation with good enantioselectivity and in good yield under simple and mild conditions. We have applied this new process to a streamlined, catalytic asymmetric synthesis of a bioactive α-fluoroamide and to the synthesis of other classes of enantioenriched fluorinated compounds.
More Related Videos
10:42Preparation of N-2-alkoxyvinylsulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
Published on: January 3, 2018
10:10Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes
Published on: July 28, 2018
Related Concept Videos
α-Alkylation of Ketones via Enolate Ions
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
Amines to Alkenes: Hofmann Elimination
Under thermal conditions, the hydroxide can abstract a proton from the β carbon; this generates an alkene with the simultaneous...
Synthesis of α-Substituted Carbonyl Compounds: The Stork Enamine Reaction
Acid-Catalyzed α-Halogenation of Aldehydes and Ketones
In the first step of the mechanism, the acid protonates the carbonyl oxygen resulting in a resonance-stabilized cation, which subsequently loses an α-hydrogen to form an enol tautomer. The C=C bond in an enol is highly nucleophilic because of the electron-donating nature of the –OH group. Consequently, the double bond attacks an electrophilic halogen to form a...
Base-Promoted α-Halogenation of Aldehydes and Ketones