Asymmetric Fluorination Reactions promoted by Chiral Hydrogen Bonding‐based Organocatalysts

Fluorinated compounds can exhibit interesting biological properties. The importance of these species has made that the chemistry of fluorine has experienced a great development. On this review, the recent advances on asymmetric fluorination reactions promoted by chiral hydrogen bonding‐based organoc...

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Published in:Advanced synthesis & catalysis 2020-12, Vol.362 (23), p.5275-5300
Main Authors: Auria‐Luna, Fernando, Mohammadi, Somayeh, Divar, Masoumeh, Gimeno, M. Concepción, Herrera, Raquel P.
Format: Article
Language:English
Subjects:
(thio)urea
Asymmetry
Biological properties
Carboxylic acids
Chemical bonds
Fluorination
Fluorine
Hydrogen bonding
hydrogen-bond
organocatalysis
Phosphoric acid
squaramide
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description Fluorinated compounds can exhibit interesting biological properties. The importance of these species has made that the chemistry of fluorine has experienced a great development. On this review, the recent advances on asymmetric fluorination reactions promoted by chiral hydrogen bonding‐based organocatalysts are discussed. Hence, examples using phosphoric acid, carboxylic acid, (thio)urea and squaramide derivatives are illustrated. The growth of this field is amazing. We have only considered pivotal works in which direct fluorination takes place using a fluorinating agent, leaving aside the reactions where a fluorine atom is incorporated from the beginning as part of other reactants. Herein, the scarce existing examples on this field of research have been compiled.
doi_str_mv 10.1002/adsc.202000848
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subjects (thio)urea
Asymmetry
Biological properties
Carboxylic acids
Chemical bonds
Fluorination
Fluorine
Hydrogen bonding
hydrogen-bond
organocatalysis
Phosphoric acid
squaramide
title Asymmetric Fluorination Reactions promoted by Chiral Hydrogen Bonding‐based Organocatalysts
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