4.4 Review

Recent Progress in Asymmetric Fluorination and Trifluoromethylation Reactions

Journal

CURRENT TOPICS IN MEDICINAL CHEMISTRY
Volume 14, Issue 7, Pages 901-940

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1568026614666140202205531

Keywords

Fluorine; fluorination; trifluoromethylation; chirality; asymmetric synthesis

Funding

  1. CNRS
  2. University of Rouen
  3. INSA of Rouen
  4. Tianjin University
  5. NSFC [21172170, 21225208]

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All domains of society are impacted by fluorine chemistry. In particular, fluorine plays a key role in medicinal, pharmaceutical and agrochemical sciences in which the synthesis and evaluation of molecules featuring one or more fluorine atoms is nowadays routine in every new discovery and development program. Since the beginning of this century, enantiopure fluorinated molecules are at the forefront of innovation of the tremendous achievements in fluorine chemistry. This review introduces the reader to the recent progress in asymmetric installation of one fluorine and a trifluoromethyl group via nucleophilic, electrophilic and radical diastereo- and enantioselective reactions.

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