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Electrochemical Partial Fluorination of α, β -Unsaturated Esters

  • Norihiko Yoneda
Conference paper

Abstract

A novel electrochemical partial fluorination of α, β-unsaturated esters efficiently took place accompanied by the rearrangement of the β-substituted alkyl groups to the α-position to afford gem-β,β-difluoroesters in good yields under the pulse electrolysis conditions using Et3N-5HF electrolyte.

Keywords

High Energy Efficiency Carboxylic Ester Unsaturated Ester Ring Expansion Fluorine Chemistry 
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Copyright information

© Springer Japan 1998

Authors and Affiliations

  • Norihiko Yoneda
    • 1
  1. 1.Division of Molecular Chemistry, Graduate School of EngineeringHokkaido UniversitySapporo 060Japan

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